CXCL10 deficiency limits macrophage infiltration, preserves lung matrix, and enables lung growth in bronchopulmonary dysplasia

Hirani, Dharmesh V.; Thielen, Florian; Mansouri, Siavash; Danopoulos, Soula; Vohlen, Christina; Haznedar-Karakaya, Pinar; Mohr, Jasmine; Wilke, Rebecca; Selle, Jaco; Grosch, Thomas; Mizik, Ivana; Odenthal, Margarete; Alvira, Cristina M.; Kuiper-Makris, Celien; Pryhuber, Gloria S.; Pallasch, Christian; van Koningsbruggen-Rietschel, S.; Al-Alam, Denise; Seeger, Werner; Savai, Rajkumar; Dötsch, Jörg; Alejandre Alcazar, Miguel A.

doi:10.1186/s41232-023-00301-6

Research article
Open access
Published: 24 October 2023

CXCL10 deficiency limits macrophage infiltration, preserves lung matrix, and enables lung growth in bronchopulmonary dysplasia

Dharmesh V. Hirani^1,2^na1,
Florian Thielen¹^na1,
Siavash Mansouri³,
Soula Danopoulos⁴,
Christina Vohlen^1,2,5,
Pinar Haznedar-Karakaya¹,
Jasmine Mohr¹,
Rebecca Wilke¹,
Jaco Selle¹,
Thomas Grosch¹,
Ivana Mizik¹,
Margarete Odenthal^6,7,
Cristina M. Alvira⁸,
Celien Kuiper-Makris^1,6,
Gloria S. Pryhuber⁹,
Christian Pallasch¹⁰,
S. van Koningsbruggen-Rietschel⁵,
Denise Al-Alam⁴,
Werner Seeger^2,3,
Rajkumar Savai^2,3,
Jörg Dötsch⁵ &
…
Miguel A. Alejandre Alcazar ORCID: orcid.org/0000-0002-3176-0411^1,2,6,11

Inflammation and Regeneration volume 43, Article number: 52 (2023) Cite this article

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Abstract

Preterm infants with oxygen supplementation are at high risk for bronchopulmonary dysplasia (BPD), a neonatal chronic lung disease. Inflammation with macrophage activation is central to the pathogenesis of BPD. CXCL10, a chemotactic and pro-inflammatory chemokine, is elevated in the lungs of infants evolving BPD and in hyperoxia-based BPD in mice. Here, we tested if CXCL10 deficiency preserves lung growth after neonatal hyperoxia by preventing macrophage activation. To this end, we exposed Cxcl10 knockout (Cxcl10^−/−) and wild-type mice to an experimental model of hyperoxia (85% O₂)-induced neonatal lung injury and subsequent regeneration. In addition, cultured primary human macrophages and murine macrophages (J744A.1) were treated with CXCL10 and/or CXCR3 antagonist. Our transcriptomic analysis identified CXCL10 as a central hub in the inflammatory network of neonatal mouse lungs after hyperoxia. Quantitative histomorphometric analysis revealed that Cxcl10^−/− mice are in part protected from reduced alveolar. These findings were related to the preserved spatial distribution of elastic fibers, reduced collagen deposition, and protection from macrophage recruitment/infiltration to the lungs in Cxcl10^−/− mice during acute injury and regeneration. Complimentary, studies with cultured human and murine macrophages showed that hyperoxia induces Cxcl10 expression that in turn triggers M1-like activation and migration of macrophages through CXCR3. Finally, we demonstrated a temporal increase of macrophage-related CXCL10 in the lungs of infants with BPD. In conclusion, our data demonstrate macrophage-derived CXCL10 in experimental and clinical BPD that drives macrophage chemotaxis through CXCR3, causing pro-fibrotic lung remodeling and arrest of alveolarization. Thus, targeting the CXCL10-CXCR3 axis could offer a new therapeutic avenue for BPD.

Introduction

Bronchopulmonary dysplasia (BPD) is a chronic lung disease of the premature infant who often requires life-saving respiratory support such as supplemental oxygen and/or mechanical ventilation due to the immaturity of the lung. Despite significant advances in neonatal management and improved survival, BPD still occurs in up to 40% of infants born less than 29 weeks gestation [1]. Lungs of infants with BPD are characterized by alveolar and vascular hypoplasia that results in an emphysema-like lung structure that is evident beyond infancy. Extracellular matrix (ECM) is essential for alveolar formation by providing the "framework" for resident lung cells, regulating cellular signaling, and maintaining lung elasticity as well as the alveolar integrity [2, 3]. In contrast, perturbed assembly and increased degradation of the lung matrix favoring fibrosis are hallmarks of severe BPD [4,5,6,7].

Inflammation is central in the pathogenesis of BPD and a main regulator of lung matrix remodeling, but the mechanisms remain elusive. Previous studies have shown elevated concentrations of pro-inflammatory cytokines and chemokines, e.g., IL17, CCl7, CXCL5, and CCL2, in the lungs of infants with BPD [8,9,10]. Recent studies from our group demonstrated an activation of macrophages along with IL-6 signaling in human lungs with BPD as well as in the lungs of neonatal mice exposed to prolonged hyperoxia as a model of the BPD [8]. Excessive activation and recruitment of macrophages in murine lungs after hyperoxia caused apoptosis of epithelial cells, reduced alveolarization, and failed angiogenesis, ultimately aggravating the pathogenesis of BPD and resulting in a poor clinical outcome [10, 11]. Moreover, cross-talk of activated macrophages with fibroblasts also accompanies perturbed and increased ECM deposition [12,13,14,15,16,17,18] and might lead to irreversible matrix changes with aberrant lung growth in neonatal mice.

Various factors trigger the migration of activated macrophages in the lung, e.g., chemokines and cell adhesion molecules [19]. For example, the C-X-C motif chemokine 10 (CXCL10), also known as IFN-γ–induced protein (IP-10), binds to the CXCR3 receptor, triggers chemotaxis, cell growth as well as apoptosis [20, 21]. CXCL10 also modulates immune responses by recruiting inflammatory cells [i.e., neutrophils, T lymphocytes, and natural killer (NK) cells] to the sites of inflammation [22, 23]. Interestingly, CXCL10 is not only secreted by macrophages but also activates and attracts macrophages into tissues, and thus CXCL10 substantially controls the inflammatory response as well as the tissue and matrix homeostasis [24,25,26]. In contrast, either neutralization of CXCL10 or blockage of CXCR3 reduces the recruitment of immune cells, e.g., macrophages, thereby mitigating the inflammatory pulmonary and perivascular response [19, 27]. Initial studies indicate a controversial role of CXCL10 in the fibrotic processes. While CXCL10 has been described to act as an anti-fibrotic chemokine in an experimental model of bleomycin-induced lung fibrosis, it promotes liver fibrosis [28, 29]. However, the functional role of CXCL10 in BPD has not been addressed to date and remains elusive.

In the present study, the transcriptomic analysis identified an inflammatory profile in neonatal lungs after hyperoxia with a marked lung-intrinsic increase of Cxcl10 together with macrophage recruitment to the lung. In contrast, transgenic mice with Cxcl10 deficiency were in part protected from macrophage influx to the lung, epithelial cell apoptosis, loss of alveolar epithelial type 2 cells (AT2), perturbed elastic fiber deposition, and increased collagen deposition. Of note, these findings were not only found in hyperoxia-induced acute injury at postnatal day 14 (P14) but persisted during regeneration in normoxia at P28. Mechanistically, we show that the blockage of the CXCR3 receptor reduces the CXCL10-mediated human and murine macrophage invasion. Finally, the lungs of infants with BPD showed an age-dependent increase of macrophages that was related to a macrophage-specific elevation of CXCL10.

Results

Transcriptomic analysis identified Cxcl10 as a central hub in hyperoxia-induced inflammation in newborn mice at postnatal day 14 (P14)

Hyperoxia promotes inflammation through the alteration of cytokine and chemokine signaling pathways in the lungs of neonatal mice. We recently identified an important role of macrophages in the pathogenesis of BPD using the RNA sequencing (RNA-Seq)-based transcriptomic profiling [8]. To further investigate central signaling hubs in the lung inflammatory response after hyperoxia, we now analyzed our publicly available lung bulk RNA-Seq data from newborn mice exposed to hyperoxia for 14 days (Fig. 1A). In the present study, the top 25 up and down-regulated differentially expressed genes (DEG) (Supplementary Table 1) were taken into account as depicted in the heatmap in Fig. 1B. Subsequently, an online open-source platform called SRPLOT (https://www.bioinformatics.com.cn/en) was used for in-silico data analysis and visualization. We performed KEGG pathway annotation analysis based on the enrichment score using SRPLOT and found that pathways associated with inflammation, e.g., cytokine-cytokine receptor interaction, chemokine signaling pathways, or IL-17 signaling pathways, are amongst the significantly regulated pathways in lungs of newborn mice after hyperoxia (Fig. 1C). To identify central molecular hubs in the inflammatory network, we used DEGs associated with the top-ten KEGG pathways as input for gene ontology (GO) analysis. We visualized the interaction of the DEGs with the pathways based on GO annotation using a sneaky plot and found central DEGs, notable amongst those Cxcl10 (Fig. 1D). For validation of these findings, we next assessed gene expression of Cxcl10 in lungs at postnatal day 7 (P7) and P28 (Fig. 1E) and found a 4- to 6-fold upregulation in neonatal mouse lungs after hyperoxia at both time points. In addition, we performed a serum ELISA for CXCL10 and detected a significant reduction of CXCL10 protein after hyperoxia at P28 (Fig. 1F), indicating a lung-intrinsic upregulation of Cxcl10 as an inflammation and macrophage-regulating chemokine [19, 22, 23, 27]. In contrast, the expression of Cxcr3, the CXCL10 receptor, was not altered between normoxia and hyperoxia at P7, but significantly downregulated at P28 after a prolonged exposure to hyperoxia (Fig. 1G). Collectively, our data indicate that CXCL10 could play a central role in the inflammatory response in neonatal lungs after hyperoxia.

Loss of CXCL10 enables alveolar formation, reduces apoptosis, and protects alveolar epithelial type 2 cells (AT2) in newborn mice after hyperoxia

Next, we tested if Cxcl10 is mechanistically important in alveolarization and cell survival during acute hyperoxia-induced neonatal lung injury. To this end, wild-type (WT) or Cxcl10 knockout (Cxcl10^−/−) mice were exposed to normoxia (NOX; 21% O₂) or hyperoxia (HYX; 85% O₂) after birth for 14 days, and lungs were studied at P14 as illustrated in Fig. 2A. Neonatal hyperoxia markedly blocked alveolar formation in WT mice as indicated by an increased average surface area of a single alveolus and a reduced radial alveolar count (RAC); in contrast, Cxcl10^−/−HYX were partially protected from these effects when compared to WT^HYX (Fig. 2B-D). In addition, co-immunofluorescent staining for TUNEL (a marker for apoptotic cells) and surfactant protein C (SFTPC; a marker for AT2) showed an almost 10-fold increased number of apoptotic cells in lungs of WT^HYX that was significantly attenuated in lungs of Cxcl10^−/−HYX (Fig. 2E, F). Similarly, the loss of Cxcl10 partially protected from the reduction of SFTPC⁺ cells after hyperoxia by 50% (Fig. 2G). These data indicate a pro-apoptotic effect of CXCL10 in neonatal lungs exposed to prolonged hyperoxia that could in part explain an arrest of alveolarization observed in lungs with BPD.

Loss of CXCL10 attenuates fibrotic remodeling in hyperoxia-exposed neonatal lungs through preserved spatial elastic fiber distribution and reduced collagen deposition

Extracellular matrix (ECM) plays an important role in normal lung development and alveolar formation [2, 30]. In contrast, perturbed assembly and distribution of elastic fibers as well as increased collagen production are intimately linked to aberrant alveolarization [6, 7]. Here, we show a significant increase of septal thickness in WT^HYX, indicating increased ECM deposition. In contrast, Cxcl10^−/−NOX and Cxcl10^−/−HYX exhibited a reduced septal thickness when compared to WT^NOX and WT^HYX, respectively (Fig. 3A, B). We next studied the deposition of matrix components in the neonatal lung after hyperoxia. First, we found a reduction of elastic fiber fraction in the lungs of WT^HYX and Cxcl10^−/−HYX when compared to WT^NOX and Cxcl10^−/−NOX, respectively. While elastic fibers are predominantly localized at the tip of the secondary crests in lung lungs of WT^NOX, in neonatal WT^HYX lungs, we found them as “brushed-like” structures in the primary septae and not at the tip of the secondary septae as previously described [5]. Interestingly, Cxcl10^−/−HYX were not protected from the reduced abundance of elastic fibers, but the spatial distribution was predominantly at the tip of the secondary crests (Fig. 3A, C). Since elastic fibers and collagen are interrelated in lung matrix biology, we next performed Sirius red staining as an indicator of collagen. Hyperoxia induced a more than 3-fold increase of collagen in lungs from WT mice, whereas Cxcl10^−/−HYX was partially protected when compared to WT^HYX (Fig. 3D, E). To further understand the mechanisms by which elastic fiber and collagen synthesis as well as deposition are regulated, we assessed the activity of two key matrix metalloproteinases (MMP), MMP2 and MMP9, using zymography. The analysis revealed that hyperoxia significantly induced the activity of MMP2 in both WT and Cxcl10^−/− mice. In contrast, MMP9 activity was not increased in neonatal lungs of WT^HYX when compared to WT^NOX. Lungs of Cxcl10^−/−HYX, however, exhibited a 2-fold higher MMP9 activity than lungs of Cxcl10^−/−NOX or WT^NOX (Fig. 3F, G). TGFβ signaling plays a central role in lung fibrotic processes and matrix remodeling. Since prior studies from our group showed an activation of the TGFβ pathways in neonatal lungs after hyperoxia, we now assessed phosphorylated SMAD2 (pSMAD2) as a downstream effector of TGFβ [4, 30]. Immunoblot for pSMAD2 and total SMAD2 showed an almost 10-fold activation of pSMAD2 in the lungs of WT^HYX, whereas this effect was attenuated by almost 50% in lungs of Cxcl10^−/−HYX, indicating a pro-fibrotic function of CXCL10 in neonatal lungs after hyperoxia (Fig. 3H, I). Interestingly, the gene expression of key collagens (Col1a1, Col3a1, and Col4a4) (Supplementary Fig. 1A-C), were not significantly regulated by CXCL10, suggesting that the pro-fibrotic effect might be primarily mediated through an imbalance of lung matrix assembly, deposition, and degradation through proteolytic activity. Collectively, these data show that CXCL10 has a modulatory function on elastic fiber assembly as well as localization and a pro-fibrotic effect through the regulation of MMP9 and TGFβ signaling.

Loss of CXCL10 limits macrophage influx into neonatal lungs after hyperoxia

Since CXCL10 acts as a chemoattractant for macrophages, we next tested if the loss of CXCL10 may reduce hyperoxia-induced macrophage influx to the lung. To this end, we performed immunohistochemical staining for CD68, a marker of active macrophages, and found a significantly increased number of macrophages in lungs of WT^HYX when compared to WT^NOX. In contrast, Cxcl10^−/−, however, were protected from macrophage influx in neonatal lungs after hyperoxia (Fig. 4A, B). Moreover, the expression of CXCL10 receptor Cxcr3 increased in WT^HYX and was attenuated in Cxcl10^−/−HYX (Fig. 4C). Moreover, the mRNA expression of the CC-chemokine ligand 2 (Ccl2; monocyte chemotactic protein 1) was more than 20-fold increased in WT^HYX when compared to WT^NOX, whereas loss of CXCL10 significantly reduced this effect (Fig. 4D). The expression of the M1-like macrophage marker Tnfa, but not Il1b was higher in Cxcl10^−/−HYX when compared to Cxcl10^−/−NOX or WT^HYX (Supplementary Fig. 1D, E). The gene expression of M2-like macrophages (Arg1 and Il4) was neither affected in WT or Cxcl10^−/− exposed to normoxia or hyperoxia (Supplementary Fig. 1F, G). On the contrary, we found a significant higher mRNA expression of Lgals3 and C1qb in CXCL10^−/−HYX when compared to WT^HYX (Fig. 4E, F). Galectin3 (Lgals3) and C1qb have been described to regulate migration/chemotaxis [31, 32] and to limit inflammasome activity [33], respectively. These results strengthened the notion that CXCL10 acts as a central hub of the immune response in neonatal lungs after hyperoxia through chemoattraction of macrophages with subsequent release of cytokines that can affect inflammation, cell survival and lung matrix remodeling.

The beneficial effect of CXCL10 deficiency on alveolarization and lung matrix in lungs of neonatal mice exposed to hyperoxia persists after a regeneration phase

The preceding findings demonstrate that CXCL10 is important in the hyperoxia-induced arrest of alveolarization through a regulation of macrophage invasion, the inflammatory response, cell survival, and lung matrix remodeling. However, the impact of CXCL10 during regeneration after neonatal hyperoxia has not been addressed to date. Therefore, we exposed WT and Cxcl10^−/− mice to either normoxia (21% O₂) or hyperoxia (85% O₂) from birth until P14, followed by recovery in normoxia for the next 14 days until P28 as shown in Fig. 5A. First, the quantitative histomorphometric analysis revealed a persistent increased average surface area of a single alveolus and a reduced RAC in WT^HYX when compared to WT^NOX at P28, indicating an irreversible arrest of alveolarization after hyperoxia. In contrast, loss of CXCL10 partially preserved alveolar formation as indicated by a lower average surface area of a single alveolus and an increased RAC in Cxcl10^−/−HYX when compared to WT^HYX (Fig. 5B-D). Next, we measured gene expression of collagens (Col1a1, Col3a1, and Col4a4) and did not detect any differences between WT^HYX and WT^NOX. However, Col1a1 was significantly reduced Cxcl10^−/−HYX when compared to Cxcl10^−/−NOX. Similarly, Col4a4 was lower in Cxcl10^−/−HYX than in WT^HYX (Supplementary Fig. 2A-C). Alveolar septae remained threefold thicker in WT^HYX than in WT^NOX even after recovery, whereas the septal thickness was attenuated by approximately 50% in Cxcl10^−/−HYX when compared to WT^HYX (Fig. 5E). To further substantiate the notion that changes in septal thickness is caused by lung matrix remodeling, we next assessed elastic fibers and collagen in the lungs. Interestingly, in contrast to P14, WT^HYX exhibited up to a 3-fold increase of elastic fibers relative to lung tissue in comparison to WT^NOX at P28, and the spatial distribution remained perturbed with “brush-like” structures. In Cxcl10^−/−HYX, however, the elastic fiber fraction was attenuated when compared to WT^HYX and the spatial distribution remained at the secondary crests with less “brush-like” structures than WT^HYX (Fig. 5F, H). Similar to the findings in lungs after acute injury at P14, WT^HYX continued with a marked increase in collagen deposition relative to lung tissue when compared to WT^NOX at P28, whereas loss of CXCL10 fully protected from these effects (Fig. 5G, I). It is noteworthy, that Cxcl10^−/−NOX showed a significantly higher elastic fiber and lower collagen content than WT^NOX (Fig. 5H, I), further supporting the notion that CXCL10 plays a vital role in lung matrix remodeling, not only during acute injury, but also during regeneration.

Loss of CXCL10 limits macrophage influx into the lung during regeneration from neonatal hyperoxia

Activated macrophages regulate lung matrix remodeling that can adversely affect alveolar development. Thus, preventing the migration of macrophages to the lung could not only preserve normal lung matrix synthesis and assembly but thereby also promote alveolar growth. We assessed the number of activated macrophages in the lungs after recovery from neonatal hyperoxia at P28 using immunohistochemical staining for CD68 and found an almost 2-fold increase of macrophages in WT^HYX when compared to WT^NOX. Cxcl10^−/−HYX, however, were significantly protected from the increase of macrophages during regeneration after neonatal hyperoxia when compared to WT^HYX (Fig. 6A, B). The increase of macrophage invasion in WT^HYX was related to a persistent increase of Cxcl10 expression in lungs at P28 after recovery from HYX (Supplementary Fig. 3). Interestingly, in contrast to P14, we did not determine changes in the gene expression of Cxcr3, the CXCL10 receptor, in WT or Cxcl10^−/− at P28 after neonatal hyperoxia. (Fig. 6C). However, the mRNA expression of Ccl2 was significantly reduced in Cxcl10^−/−NOX and by trend in Cxcl10^−/−HYX when compared to WT^NOX and WT^HYX, respectively (Fig. 6D). Moreover, we assessed pro-inflammatory markers and found a significant reduction of Tnfa by 50% in Cxcl10^−/−HYX when compared to WT^HYX. Similarly Il1b mRNA was markedly lower in in Cxcl10^−/−HYX than in Cxcl10^−/−NOX. On the other hand, M2-like macrophage markers (Arg1, Il4) were not altered by hyperoxia or Cxcl10^−/− (Supplementary Fig. 4A-D). Interestingly, Lgals3 was significantly downregulated in WT^HYX when compared to WT^NOX, whereas this effect was attenuated in Cxcl10^−/−HYX. Lgals3 encodes for Galectin3, a protein that limits invasion of immune cell; a loss of Galectin3 expression as seen in WT^HYX but not in Cxcl10^−/−HYX could partly explain increased macrophage invasion in WT but not Cxcl10^−/− after hyperoxia (Fig. 6E). Next, we measured the gene expression of C1qb, encoding for a protein with anti-inflammasome function, and found a significant increase in Cxcl10^−/−NOX when compared to WT^NOX lungs (Fig. 6F). Our data indicate that CXCL10 is a key regulator of macrophage function, and its effect is dependent on the microenvironment and exposome. While loss of CXCL10 promotes macrophage invasion to the lung under normoxia, the macrophages do not seem to be polarized towards a pro-inflammatory sub-type. Conversely, knockout of CXCL10 under hyperoxia results in protection from invasion, suggesting a microenvironment-modulated CXCL10-dependent differentiation of macrophages.

Hyperoxia induces Cxcl10 that drives migration of human and murine macrophages through its receptor CXCR3

Hyperoxia significantly induced mRNA expression of Cxcl10 in mouse peritoneal macrophages (J774A.1; mMΦ), confirming the impact of increased oxygen concentration on CXCL10 signaling (Fig. 7A). To further understand the possible role of a CXCL10-CXCR3 axis in the regulation of macrophage function, we first treated J774A.1 with CXCL10 (10 ng/ml) or DMSO as vehicle control for 48 h in serum-reduced medium, followed by assessment of gene expression using qRT-PCR. Stimulation with CXCL10 caused an almost 2-fold induction of Il6, Il1b, Nos2 (iNOS), and Ccl2, indicating an M1-like activation of murine macrophages (Fig. 7B, C). For the migration assay, we used the Boyden chamber assay and stimulated J7741.A with either CXCL10 (10 ng/l) [lower chamber with 1% FBS medium] alone or in combination with CXCR3 antagonist (300 nM/ml) [upper chamber with serum-reduced medium] for 24 h; DMSO served as vehicle control. Stimulation with CXCL10 induced a 2-fold increase in the migration rate of murine macrophages, whereas blocking the CXCR3 receptor significantly reduced the CXCL10-induced migration of macrophages (Fig. 7D, E). Treatment with the CXCR3 receptor antagonist alone did not affect murine macrophage migration (Supplementary Fig. 5A, B). To translate our data to human, we next used human blood monocyte-derived macrophages. Since prior studies from our group demonstrated that hyperoxia causes M1-like polarization in mouse lungs [8], we now polarized human macrophages towards M1-like phenotype by treatment with GM-CSF (100 ng/ml for 7 days with media change at alternating days) (hM1Φ; Fig. 7F). Similar to mice, exposure of hM1Φ to hyperoxia (85% O₂) for 48 h induced gene expression of CXCL10 and IL1B, whereas CCL2 was downregulated (Fig. 7G). In analogy to the mMΦ, we treated hM0Φ with either CXCL10 (10 ng/ml) alone or in combination with CXCR3 antagonist (300 nM/ml) for 24 h; DMSO served as vehicle control. The analysis of the migration assay revealed a significant increase in hM0Φ migration that was prevented by blocking the CXCR3 receptor (Fig. 7H, I); CXCR3 receptor blocker alone did not have a marked effect on macrophage migration (Supplementary Fig. 5C, D). These data do not only demonstrate that hyperoxia induces Cxcl10 expression, but also that CXCL10 further triggers M1-like inflammatory phenotype and promotes migration of macrophages.

Macrophage (CD68⁺) influx with elevated CXCL10 expression in lungs of infants with BPD

Finally, we analyzed the lungs of age-matched infants with or without BPD (Table 1). To this end, we first performed immunofluorescent staining for CD68 (marker of activated macrophages) combined with in situ hybridization of CXCL10. Lungs with BPD showed a significant increase of CD68⁺ cells (macrophages) per field of view with age when compared to non-BPD lungs (p = 0.0185) (Fig. 8A, B). Subsequent quantification showed a decrease in the intensity of CXCL10 per DAPI⁺ cell in non-BPD lungs with age, whereas the intensity of CXCL10 per DAPI⁺ cell increased significantly in BPD lungs with age (R² = 0.9495; p = 0.0049) (Fig. 8C). In addition, the intensity of CXCL10 per CD68⁺ cell was significantly higher in lungs with BPD than in non-BPD lungs with age (R² = 0.8706; p = 0.0206) (Fig. 8D). In summary, these findings support the hypothesis that hyperoxia-induced activation of CXCL10 signaling in M1-like macrophages could contribute to the progression of BPD over time.

Table 1 Clinical data of lungs of infants with and without bronchopulmonary dysplasia (BPD)

Full size table

Discussion

The present study investigates the role of the CXCL10-CXCR3 signaling in the inflammatory response and macrophage influx in experimental and clinical BPD. In a murine model of hyperoxia-induced neonatal lung injury, transcriptome analysis identified CXCL10 as a central hub in lung inflammation of neonatal mice exposed to hyperoxia. Neonatal Cxcl10 null mice were protected from (i) macrophage influx to the lung, (ii) lung matrix remodeling with increased collagen deposition and perturbed spatial distribution of elastic fibers as well as (iii) lung cell apoptosis and loss of AT2, (iv) thereby preserving alveolar formation during hyperoxia-induced acute lung injury. Analysis of murine and human macrophages revealed a hyperoxia-induced M1-like differentiation and a CXCR3-mediated macrophage migration. Finally, our data demonstrate an increased CXCL10 expression in macrophages over time in the lungs of infants with BPD vs non-BPD, offering CXCL10-CXCR3 as a potential target for inflammation-driven progression of BPD.

Inflammation is important in the pathogenesis of BPD [9, 34, 35]. In particular, macrophages accumulate in the lungs of infants with BPD as well as in hyperoxia-induced lung injury as a model of BPD [8]. While recent studies report multiple macrophage subtypes along with diverse immunomodulatory functions in the developing lung [36] as well as after neonatal hyperoxia [9], the mechanisms regulating macrophage homeostasis and activation remain poorly understood. Prior studies from our group showed a macrophage influx to the lung and a differentiation towards pro-inflammatory (M1-like) phenotype in neonatal mouse lungs after hyperoxia, resulting in a reduced alveolarization and an excessive epithelial cell apoptosis [8]. Our current transcriptomic approach identified CXCL10 to be central in the lung inflammatory network in neonatal mice after hyperoxia. The clinical relevance of CXCL10 was further supported by clinical studies in which elevated concentrations of CXCL10 in tracheal aspirates were associated with evolving BPD or death in premature infants [37]. In the present study, we examined the time course of CXCL10 expression in lungs of non-BPD and BPD infants. While the CXCL10 expression was high at the early stage in non-BPD lungs and decreased over time, we detected an opposite trend with a significant correlation of increasing CXCL10 expression in BPD lungs with age. Of note, this finding was associated with a higher number of macrophages as well as increased CXCL10 per macrophage in BPD when compared to non-BPD lungs. CXCL10 as a macrophage-regulating chemokine may contribute to the migration of immune cells, inflammation, and clinical course of BPD, and could thereby serve as a biomarker of BPD in very premature infants.

This notion was further supported by our experimental BPD model, where we associated hyperoxia-induced Cxcl10 with macrophage infiltration to the lung. In contrast, Cxcl10 null mice were protected from macrophage influx, resulting in an attenuated lung growth arrest. Various studies pointed out the role of CXCL10 as a chemokine that plays a critical role in the migration of immune cells, particularly T cells, NK cells, and macrophages [22, 23, 38]. Migration of immune cells is induced by the binding of CXCL10 to its receptor, CXCR3 that is expressed on the surface of T cells, NK cells, and macrophages, resulting in macrophage migration towards the site of CXCL10 production [22, 23]. Here, we demonstrate that exposure of cultured macrophages to hyperoxia increases the expression of CXCL10, which in turn increases mRNA expression of Il6, Il1b, Nos2, and Ccl2 in murine macrophages. CXCL10 signals through the CXCR3 receptor and thereby regulates the infiltration of immune cells and macrophage homeostasis in the tissue [23, 39,40,41]. Our in vitro study shows that CXCL10 drives migration of murine and human macrophages significantly, a process that is inhibited by the CXCR3 antagonist. However, other immune and epithelial cells produce different chemokines and may be involved in chemoattraction in the pathogenesis of the BPD as well [42]. Our in vitro data combined with the in vivo findings indicate a migratory and immunomodulatory role of CXCL10 in hyperoxia-induced neonatal lung injury and BPD, offering a possible target for pharmacological treatment or prevention.

Inflammation and macrophage activation can contribute to lung matrix remodeling in BPD through an interplay with other cell types, e.g., fibroblasts and epithelial cells [8, 43,44,45]. For example, reports demonstrate an important role of the imbalance in macrophage activation in the initiation of fibrotic remodeling in lungs with idiopathic pulmonary fibrosis (IPF). Moreover, a recent study showing a pro-fibrotic macrophage response in SARS-CoV2 infection points out the plasticity of macrophages and their important role in matrix remodeling and lung repair [14]. Similarly, targeting subtypes of pro-fibrotic macrophages or targeting CXCR3 limits the progression of fibrosis [46]. Collectively, these studies shed light on the role of macrophages in altering ECM composition and deposition. Studies to determine cell–cell communication between macrophages and fibroblasts could help to understand how certain signals promote fibrotic changes and differentiation of subsets of mesenchymal cell populations. For example, the CXCR3-CXCL10 axis modulates the immune cell proportion in tissue in part through the regulation of infiltration, e.g., inhibiting NK cells and anti-tumor T cells [29, 47] or promoting neutrophils and macrophages [38, 40]. An imbalance in immune cell proportion can favor a microenvironment for fibrosis-related tissue remodeling [47]. Moreover, CXCL10 secreted by activated fibroblasts plays a crucial role in triggering M1-like polarization of macrophages in an inflammatory environment [24]. It also is involved in the regulation of inflammation and immune responses, which can affect the disease progression [37, 48, 49]. Here, we observed an increased number of macrophages in the lungs of Cxcl10 null exposed to room air. The mechanisms by which CXCL10 interferes with the macrophage infiltration under physiological conditions remain unclear but could be related to an imbalance in chemoattractant chemokines and distinct polarization of macrophages. Moreover, our data demonstrate that the functional impact of CXCL10 on the expression of macrophage markers depends on the micro-environment such as the oxygen concentration. While loss of CXCL10 itself promotes macrophage invasion to the lung under normoxia, they do not seem to be polarized towards a pro-inflammatory sub-type. Conversely, knockout of CXCL10 under hyperoxia results in protection from invasion, possibly by regulating Lgals3 (Galectin3) and C1qb that limits immune cell invasion and inflammasome activity, respectively [31,32,33]. This immunomodulatory function of CXCL10 may underlie the reduced increase in septal thickness and deposition of collagen in the alveolar septa and thus may also provide an advantage for alveolar structure and function during regeneration. Our current findings suggest a distinct CXCL10-mediated differentiation of macrophages depending on oxygen concentration. Further studies are required to explore the role of CXCL10 in macrophage homeostasis and migration in healthy and different disease conditions.

CXCL10 is associated with the pathogenesis of lung diseases, including BPD and IPF [37, 50]. In contrast, experimental studies show that blocking CXCL10 has therapeutic potential [40]. The present study did not only focus on the role of CXCL10 in acute neonatal lung injury after hyperoxia, but also studied the impact of CXCL10 on lungs during the recovery from postnatal hyperoxia. We demonstrate that the simplified alveolar structure after neonatal hyperoxia persists beyond the regeneration phase and is associated with irreversible changes in the lung matrix over time. The loss of CXCL10, however, increased the lung proteolytic activity (MMP9) and inhibited fibrotic TGFβ-SMAD2 signaling, which was associated with protection of the lung from collagen deposition and perturbed elastic fiber assembly during the acute injury, but in particular during the regeneration phase. These effects could be in part mediated by a blockade of macrophage influx to lungs in neonatal mice with Cxcl10 knockout. The possible relationship between fibro angiogenetic changes and macrophage migration as well as activation has been previously reported [23, 39,40,41] and might contribute to hyperoxia-induced lung injury. Since we did not find marked changes in the gene expression of collagens in the lungs after hyperoxia, the protective effect of the Cxcl10^−/− on lung matrix remodeling could be likely related to other interrelated mechanisms, including attenuation of pro-fibrotic signaling pathways or balancing of proteolytic processes and degradation of lung matrix. In the present study, the knockout of Cxcl10 attenuates the activation of TGFβ signaling (Fig. 3H, I) and increases the proteolytic activity of MMP9. Both Cxcl10-dependent effects could change the balance of matrix synthesis, deposition, and degradation after hyperoxia favoring anti-fibrotic effects.

Conclusion

In summary, our data identified CXCL10-CXCR3 signaling to be central in the pathogenesis of hyperoxia-induced neonatal lung injury as a model of BPD and in lungs of infants with BPD. We demonstrate that hyperoxia-induced CXCL10 promotes macrophage infiltration to murine lungs possibly through CXCR3, drives collagen deposition, perturbs elastic fiber formation and positioning, causes lung cell apoptosis, and ultimately leads to reduced alveolar formation. In contrast, CXCL10 deficiency protects neonatal lungs from macrophage influx, lung matrix remodeling, and loss of AT2, enabling thereby lung growth after hyperoxia (Fig. 8 E–G). Since we show macrophage influx with increased CXCL10 expression in lungs of infants with progressive BPD, blocking CXCR3-CXCL10 could offer a new avenue to treat infants at risk for BPD and ameliorate the course of BPD.

Material and methods

Sub-analysis of our publicly available RNA sequencing (RNA-Seq) data set

For transcriptomic analysis, we used an RNA-Seq dataset of lungs of newborn mice exposed to normoxia (21% O₂, NOX) or hyperoxia (80% O₂, HYX) from birth until P14. This RNA-Seq dataset was previously published by our group and is deposited and publicly available in Dryad repository (https://doi.org/10.5061/dryad.rr4xgxd8m). Genes with p < 0.05 and fold change > 1.5-fold were considered differentially expressed genes (DEG). In the present study, first, we generated a heatmap of the 25 most up- and down-regulated DEG based on their fold change using heat mapper (http://heatmapper.ca/) [51]. For subsequent data analysis we used http://www.bioinformatics.com.cn/srplot, a free online platform for data analysis and visualization. We performed KEGG pathway annotation analysis based on the enrichment score using SRPLOT [52, 53]. For studying the inflammatory network, DEGs associated with the top-ten most up- or downregulated KEGG pathways were used as input for gene ontology (GO) analysis. Visualization of the interaction of the DEGs with the pathways based on GO annotation was performed with a sneaky plot [54, 55].

Animal studies and ethical approval

All animal studies were approved by the local government authorities (LANUV, NRW, Germany; 87–51.04.2010.A372; 84–02.04.2015.A120; 84–02.04.2020.A95). Adult and neonatal male and female C57BL/6 J (WT), as well as B6.129S4-Cxcl10tm1Adl/J (Cxcl10^−/−; Jackson laboratory; strain #: 006087) mice, were housed in humidity- and temperature-controlled rooms exposed to a 12 h dark/light cycle and were allowed food and water ad libitum.

Neonatal hyperoxia-induced lung injury model

Newborn mice were exposed to hyperoxia as described previously [56]. In brief, newborn mice were pooled and randomized to dams on the day of birth (born within 12 h of each other). Half of the litters were exposed to 85% O₂ (hyperoxia, HYX), whereas the other pups were at room air [21% O₂; normoxia, NOX]. The dams were rotated between hyperoxia and normoxia daily. Neonatal mice were exposed to hyperoxia in a 90 × 42 × 38 cm plexiglas chamber and the oxygen concentration was monitored with a Miniox II monitor (ProOx 360, Biospherix, USA). The study design comprised two sets of experiments: (i) neonatal mice were exposed to hyperoxia or normoxia from birth until postnatal day 14 (P14); and (ii) after exposure to hyperoxia from birth until P14, mice were transferred to normoxia for regeneration until P28; the control mice were in normoxia from birth until P28. At the end of both time points (P14 and P28), lungs were excised and studied.

Tissue preparation

We sacrificed the mice and excised the lungs at P14 and P28 as previously described [56,57,58]. After ligation of the right bronchus, the right lung was excised and immediately snap-frozen and stored at -80 °C for molecular assessment; the left lung was pressure-fixed with 4% paraformaldehyde (PFA) in phosphate-buffered saline (PBS), followed by paraffin embedding as described in prior studies from our group [57].

Quantitative histomorphometric analysis

PFA-fixed and paraffin-embedded lung sections were used for quantitative histomorphometric analysis as previously described by [8]. Briefly, Isotropic Uniform Random (IUR) sectioning was performed to obtain 3 µm lung sections. Afterwards, four tissue sections were randomly chosen for hematoxylin and eosin (H&E) staining [59]. For imaging, the stained lung sections were scanned with a slide scanner (Leica SCN400 Slide Scanner, Houston, USA), followed by measurement of histomorphometric parameters in up to ten fields of view per lung Sect. (20x) as described previously [8]: radial alveolar count (RAC), average surface area of a single alveolus, and septal thickness. Fields of view were not analyzed when airways or vessels covered approximately more than 15% or lungs were atelectatic or not well inflated.

RNA isolation and quantitative reverse transcriptase PCR (RT-PCR)

Lung tissue, mouse ascites macrophages (J774A.1), and human primary macrophages were used for RNA extraction as described previously [56]. For subsequent cDNA synthesis, 1 μg of mRNA of each sample was used. For measurement of gene expression, quantitative RT-PCR (qRT-PCR) was performed in 96 well plates (FrameStar, 96 well plate #4ti-0770/C, UK) with DNA-DYE (GoTaq® qPCR Master Mix, #A600A, Madison, USA or Platinum™ Quantitative PCR SuperMix-UDG w/ROX, #11743500, Netherlands) using a 7500 Real-Time PCR System (Applied BiosystemsTM, Foster City, USA) as previously described [59]. The Primers were designed using Primer Express Software 3.0 (Applied BiosystemsTM, Foster City, USA) and sequences are listed in Supplementary Table 2. Gene expression was quantified based on the ΔΔCt-method and expressed as fold induction of mRNA expression. The housekeeping gene 18 s rRNA was used to normalize genes of interest.

Immunoblot

Proteins were isolated from snap-frozen lungs and the concentration was measured for immunoblots as described previously [59]. In brief, a concentration of 20 µg of protein per sample was separated using SDS-PAGE and transferred onto a nitrocellulose membrane. Afterwards, the membrane was blocked with 5% milk (Roth, #T145.3, Germany) and 2% bovine serum albumin (BSA; Roth, # 8076.3, Germany) in TBS-Tween (0.1% Tween®20; Sigma Aldrich, #P1379, Germany). Next, the membrane was probed with primary antibodies at 4° C overnight: rabbit anti-phosphorylated SMAD2 (pSMAD2 (Ser465/467; 138D4; Cell Signaling, # 3108, Danvers, USA, 1:1000), rabbit anti-total SMAD2 (D43B4; Cell Signaling, # 5339, Danvers, USA, 1:1000), mouse anti-β-ACTIN (Cell Signaling, #3700, Danvers, USA, 1:10,000). Next day, after washing, horseradish-peroxidase (HRP)-linked secondary antibody (anti-mouse IgG, HRP-linked antibody, #7076 or anti-rabbit IgG, HRP-linked antibody, #7074, Cell Signaling, Danvers, MA, USA) was applied at room temperature (RT) for 1 h. Protein bands were visualized using ChemiDoc XRS + Imaging System (Bio-Rad Laboratories GmbH, Germany). Densitometric analysis was performed using Image Lab software 5.2.1 (Bio-Rad Laboratories GmbH, Germany) to quantify protein amounts as previously described [57].

CXCL10 ELISA

As described previously serum samples were collected and protein concentration was measured and used for assessment of CXCL10 serum concentration using commercially available ELISA kit. The ELISA was performed according to the manufacturer’s guidance (Mouse IP-10, CXCL10, SimpleStep ELISA® Kit, Abcam, #ab214563). In brief, the ELISA plate was incubated with CXCL10 capture antibody at 4 °C overnight; afterwards, a 100 μl protein sample was added per well and incubated at RT for 2 h. The wells were then washed with washing buffer and 100 μl of the detection antibody was added to each well and incubated at RT for 1 h. Next, each well was washed and exposed to 100 μl of avidin-HRP conjugated antibody for 30 min at RT. Finally, after washing, additional 100 μl of TMB solution (substrate for avidin-HRP) was added per well and incubated for 15 min; the reaction was then stopped by the stop solution (2N H₂SO₄). In the end, the optical density (OD) was measured at 450/570 nm (Tecan Infinite® 200 PRO, Switzerland).

Zymography for detection of matrix metalloproteinase 2 (MMP2) and MMP9

Proteins from total lung homogenates were isolated in PBS, concentration was measured, and 30 μg protein per sample was used for zymography as previously described [59]. Briefly, first, the proteins were incubated with the 3.5X loading buffer (0,22 M TRIS pH 6,8; 35% Glycerol; 7% SDS; Bromphenolblue) for 10 min at RT, followed by protein separation using SDS-PAGE gel. The separation gel was supplemented with 2 mg/ml gelatin (G2500 Sigma-Aldrich, Germany) as a substrate for MMP2 and MMP9. After the protein separation, the gel was incubated in 1X renaturation buffer (25% TritonX-100) for 30 min at RT. Next, the gel was treated with the development buffer (0,5 M TRIS; 2 M NaCl; 50 nM CaCl₂; 0,2% Brij-35; pH 8,0) for 30 min at RT, and then overnight at 37 °C. To visualize the degradation of the gelatin as an indicator of MMP2 and MMP9 activity during development, the gel was then incubated with Coomassie staining solution (0,1% Coomassie Brilliant Blue; 25% Isopropanol; 10% acetic acid) for 30 min at RT. Excess Coomassie staining solution was removed by washing in dH₂O. The bands of degraded gelatin were determined with UV transillumination using a ChemiDoc XRS + Imaging System and Image Lab™ software (Bio-Rad Laboratories GmbH, Germany). The bands were analyzed by densitometry. For this purpose, the program Image Lab™ was used to generate a negative image of the zymogram, after which the band density was measured.

TUNEL and SFTPC immunofluorescent staining

Co-immunofluorescent staining was performed as previously described [8]. In brief, tissue sections were deparaffinized and rehydrated, followed by antigen retrieval with proteinase K solution (Thermo Scientific™, #EO0491, Waltham, MA, USA) for 15 min at 37 °C. Using Sea Block (Thermo Scientific™, #37527, Waltham, MA, USA), tissue sections were blocked. Then, the lung sections were incubated with terminal uridine deoxynucleotidyl transferase dUTP terminal nick end labeling (TUNEL) solution as per the manufacturer’s instructions (In Situ Cell Death Detection Kit, Roche, #11684795910, Germany) for 1 h at 37 °C. Subsequently, the sections were washed with PBS-T and incubated with rabbit anti-pro-SFTPC antibody (Merck, #AB3786, Germany, 1:200) in dark at 4 °C overnight. The next day, the sections were washed with PBS-T and treated with a secondary antibody conjugated with CY3 (Dianova, #111–165-003, USA) for 1 h at RT; cell nuclei were stained with DAPI (Sigma-Aldrich, #D9542, Germany). Finally, the tissue sections were mounted and images were taken directly at 40 × and 100 × magnification using a fluorescence microscope (Olympus, Hamburg, Germany). Images were used to calculate the total TUNEL⁺ and SFTPC⁺ cells in four fields of view per animal.

Immunohistochemical staining

Tissue sections were deparaffinized and rehydrated as previously described [8]. Afterwards, antigen retrieval was performed by cooking slides with 10 mM Citrate buffer pH 6 (Dako, Cat. No. S2369, Germany) at 99 °C for 25 min. Next, the tissue sections were treated with a blocking solution (Sea Block, Thermo Scientific™, Cat. No. 37527, Netherlands) at RT for 1 h. Slides were incubated overnight with the primary antibody rabbit anti-CD68 (Abcam, Cat. No. ab125212, UK, 1:200) at 4 °C. Next, the slides were washed with PBS and then exposed to the secondary antibody (Histofine® MOUSESTAIN KIT, Nichirei, #414341F, Japan, for rabbit primary antibody) for 1 h at RT, followed by mounting using Neo-Mount® (Merck, #109,016, Germany). The whole tissue section was scanned with a slide scanner (Leica SCN400 Slide Scanner, Houston, USA). CD68⁺ cells (macrophages) were counted in up to ten fields of view per slide and randomly selected lung sections per animal from 5–7 animals per group were analyzed.

Picro Sirius-Red staining

Lung matrix remodeling, including collagen deposition and fibrotic processes, was analyzed using Picro Sirius-Red staining. First, sections were deparaffinized, rehydrated and washed in distilled water. Then, they were immersed for 4 min in a 0.2% phosphomolybdic acid solution and then stained for 75 min with a Picro Sirius-Red solution as described previously [59]. After washing twice in 0.5% acetic acid, the sections were dehydrated with EtOH [2 × 100% (vol/vol) EtOH] and clarified in Neo-Clear to be subsequently covered. Imaging of the tissue section was performed with a slide scanner (Leica SCN400 Slide Scanner, Houston, USA). Two to four sections per animal were used for staining and up to 6 fields of view per section were analyzed.

Hart’s elastin stain

Lung sections were stained for elastic fibers (purple) using Resorcin Fuchsin from Weigert (Weigert’s Iron Resorcin and Fuchsin Solution; Carl Roth, X877.3) and counterstained yellow with Tartrazine [0.5% in 0.25% acetic acid (Dianova, cat. no. TZQ999, USA)]. After washing with PBS, slides were dehydrated with EtOH and slides were covered with mounting media.

Semi-quantitative analysis of lung collagen and elastic fiber content

Quantification of the collagen and elastic fiber content in the lung tissue was performed with ImageJ [60]. For this purpose, a light microscope (BX43; Olympus, Germany) was used; after white-balance, images of up to ten fields of view at 20 × magnification per lung section were taken applying a constant exposure time. We next set a uniform color threshold for the ImageJ2 software [61] to differentiate between elastic fibers (Hart’s stain) or collagen (Picro Sirius-Red stain) and lung tissue (Hue: 160–255; Saturation: 31–255; Brightness: 70–255). First, images were converted to RGB, and blue color images were selected for further analysis. Next, the threshold was set to cover the whole lung tissue area in the field of view; this value was considered the threshold value. The positive-stained area was defined manually as elastic fibers or collagen; next, the total elastic fiber or collagen-positive area was measured and related to the total area of tissue on the slide. The elastic fiber content is relative to the total tissue and served as a surrogate parameter for elastic fiber density (elastic fiber fraction). Similarly, the collagen content was related to the total tissue area and served as an indicator of fibrosis (collagen fraction). Large bronchioles and vessels were avoided for imaging and not well-inflated tissue areas were excluded from the analysis. All images for calculation were taken at 40 × magnification using a bright field microscope (Olympus, Hamburg, Germany).

Cell culture experiments

Murine macrophages

Murine ascites macrophages (J774A.1, ATCC® TIB-67™) were cultured with DMEM (Dulbecco's Modified Eagle Medium, Gibco, #41966–029, Netherlands) supplemented with 10% FBS (serum-rich medium) and 1% Penicillin/Streptomycin (P/S) according to the recommendations of ATCC.

Human monocyte-derived macrophages and differentiation

Human blood was collected from the hospital bank (for ethical consent see below).

Human M1-like macrophages

Isolation of monocyte-derived macrophages was performed as described previously [62]. In brief, a buffy coat from the blood was collected from the hospital blood bank of the University Hospital Cologne (approval No 06.062) and a magnetic beads-containing antibody against CD14 cell marker was used. CD14⁺ cells were collected and kept in a serum-rich medium (RPMI supplemented with 10% FBS and 1% P/S). For differentiation in M1-like macrophages, CD14⁺ cells were treated with granulocyte–macrophage colony-stimulating factor (GM-CSF; 100 ng/ml; ImmunoTools, 11343123, Friesoythe, Germany) for 7 days; the media was changed on alternate days. At the end of 7 days, M1-like macrophages were cultured with GM-CSF in serum-reduced medium (1% FBS) and exposed to normoxia (21% O₂) or hyperoxia (85% O₂) for 48 h. At the end of the experiments, mRNA was isolated and gene expression was assessed by qRT-PCR.

M0 macrophages

Human macrophages were isolated from peripheral blood mononuclear cells (PBMCs) as previously described [63, 64]. Briefly, ficoll density gradient centrifugation was used for the isolation of PBMCs from buffy coats provided by the blood bank of the Universities of Giessen and Marburg Lung Center (AZ 58/15). Red blood cell (RBC) lysis buffer (BD Biosciences) was used to remove platelets and RBC followed by two washing steps with phosphate-buffered saline (PBS). Finally, macrophages were differentiated from monocytes by culturing cells in RPMI containing 2.5% human serum, 4 mML-glutamine, and penicillin/streptomycin in six-well tissue culture plates for 10 days. Next, we subjected for migration assay.

Macrophage assays and reagents

Migration assay

When murine or human M0-like macrophages were 80% confluent, they were trypsinized and used for the Boyden chamber migration assay. To this end, 100.000 cells were seeded per cell culture insert with serum-free DMEM medium. Subsequently, the inserts (upper chamber) were placed in a 24-well plate (lower chamber) with DMEM supplemented with 1% FBS + 1% P/S.

Reagents

For assessment of migration, the following treatments were used: (i) CXCL10 (10 ng/ml; R&DSystems, #466-CR050, Minneapolis, USA) was added to the well (lower chamber), (ii) CXCR3 antagonist alone (300 nm/ml; Merckmillipore, #PS372424, Darmstadt, Germany) was added to the insert; (iii) CXCR3 antagonist (300 nm/ml; Merckmillipore, #PS372424, Darmstadt, Germany) was added to the insert (upper chamber) and CXCL10 (10 ng/ml) to the well (lower chamber); (iv) DMSO served as vehicle control. Macrophages were allowed to migrate for 24 h. At the end of the experiment, H&E staining of the transwell membrane was performed to visualize; macrophages were counted per field of view, a total of eight fields of view per transwell membrane.

In situ hybridization of human lungs

Fluorescent in situ hybridization was conducted as per manufacturer’s instructions (the Advanced Cell Diagnostics RNAscope Fluorescent Multiplex Assay) with minor adjustments as described previously [8]. First, tissue sections were treated with Protease Plus. Next, tissue was incubated with a CXCL10 probe (Advanced Cell Diagnostics; #311851) for 2 h at 40 °C on protocol day 1. Afterward, section was washed with RNAscope wash buffer, and stored overnight at RT in 5X SSC. On day 2 the protocol was continued as described in the manual until the HRP blocker step was completed. Slides were then washed with RNAscope wash buffer and blocked using 3% bovine serum albumin/5% normal goat serum/0.1% Triton for at least 1 h at RT, and incubated overnight at 4 °C with primary mouse anti-CD68 (eBioscience, #14–0688-82; 1:200, San Diego, USA). The next day slides were washed with TBST and incubated for 1 h at RT with Cy5-goat-anti-mouse-conjugated secondary antibody (Jackson Immunoresearch Laboratories, Inc., West Grove, PA, USA). Slides were then counterstained using DAPI (DE571; LifeTechnologies) and mounted using ProLong Diamond Antifade Mountant (LifeTechnologies).

Statistical analysis

All measurements are expressed as mean ± standard error of the mean (SEM) and p < 0.05 denoted significant differences. To compare outcomes between two groups, we used the unpaired t-test or the Mann Whitney test. We used two-way or one-way analysis of variance followed by Sidak’s multiple comparison test if there were more than two groups. For human studies, we performed a linear regression analysis. For statistical analysis, we use the GraphPad Prism software (Software version 8.3.0).

Availability of data and materials

The datasets analysed during the current study are available in the Dryad repository (https://doi.org/10.5061/dryad.rr4xgxd8m).

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Acknowledgements

We thank the imaging facility of the Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) for their technical support.

Funding

Open Access funding enabled and organized by Projekt DEAL. This work was supported by Deutsche Forschungsgemeinschaft [1636/5–1; MAAA], Marga und Walter Boll Stiftung (210–01.03–21; 210–02-16; MAAA); Else-Kröner Fresenius Stiftung (2021_EKEA.148); Center for Molecular Medicine Cologne (CMMC; MAAA), Oskar Helene Heim Stiftung (OHH; MAAA), and University Hospital Cologne; NIH R01HL141856 (DA), NHLBI LungMAP Research Center. U01HL122681 (SD, DA), Biorepository (1U01HL122700, GP) and Data Coordinating Center (1U01HL122638, GP).

Author information

Dharmesh V. Hirani and Florian Thielen contributed equally to this work.

Authors and Affiliations

Department of Pediatric and Adolescent Medicine, Translational Experimental Pediatrics, Experimental Pulmonology, University Hospital Cologne, Faculty of Medicine, University of Cologne, Kerpener Strasse 62, Cologne, 50937, Germany
Dharmesh V. Hirani, Florian Thielen, Christina Vohlen, Pinar Haznedar-Karakaya, Jasmine Mohr, Rebecca Wilke, Jaco Selle, Thomas Grosch, Ivana Mizik, Celien Kuiper-Makris & Miguel A. Alejandre Alcazar
Universities of Giessen and Marburg Lung Center (UGMLC), member of the German Center for Lung Research (DZL), Institute for Lung Health (ILH) and Cardio-Pulmonary Institute (CPI), Gießen, Germany
Dharmesh V. Hirani, Christina Vohlen, Werner Seeger, Rajkumar Savai & Miguel A. Alejandre Alcazar
Department of Lung Development and Remodeling, Max-Planck-Institute for Heart and Lung Research, Member of the German Center for Lung Research (DZL), Bad Nauheim, Germany
Siavash Mansouri, Werner Seeger & Rajkumar Savai
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA
Soula Danopoulos & Denise Al-Alam
Department of Pediatric and Adolescent Medicine, Faculty of Medicine, University Hospital Cologne, and University of Cologne, Cologne, Germany
Christina Vohlen, S. van Koningsbruggen-Rietschel & Jörg Dötsch
Center for Molecular Medicine Cologne (CMMC), University Hospital Cologne, Faculty of Medicine, and University of Cologne, Cologne, Germany
Margarete Odenthal, Celien Kuiper-Makris & Miguel A. Alejandre Alcazar
Institute for Pathology, University Hospital Cologne, Faculty of Medicine, and University of Cologne, Cologne, Germany
Margarete Odenthal
Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA
Cristina M. Alvira
Department of Pediatrics, Division of Neonatology, University of Rochester Medical Center, Rochester, NY, USA
Gloria S. Pryhuber
Department I of Internal Medicine, Center for Integrated Oncology (CIO) Köln-Bonn, University of Cologne, Cologne, Germany
Christian Pallasch
Cologne Excellence Cluster On Stress Responses in Aging-Associated Diseases (CECAD), University Hospital of Cologne, University of Cologne, Cologne, Germany
Miguel A. Alejandre Alcazar

Authors

Dharmesh V. Hirani
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Florian Thielen
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Siavash Mansouri
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Soula Danopoulos
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Christina Vohlen
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Pinar Haznedar-Karakaya
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Jasmine Mohr
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Rebecca Wilke
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Jaco Selle
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Thomas Grosch
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Ivana Mizik
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Margarete Odenthal
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Cristina M. Alvira
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Celien Kuiper-Makris
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Gloria S. Pryhuber
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Christian Pallasch
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S. van Koningsbruggen-Rietschel
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Denise Al-Alam
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Werner Seeger
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Rajkumar Savai
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Jörg Dötsch
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Miguel A. Alejandre Alcazar
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Contributions

D.H, F.T., S.D., D.A., C.P., R.S., and M.A.A.A. conceived and designed research; D.H., F.T., S.M., S.D., C.V., P.H.K.., J.M., R.W., J.S., I.M., C.M.A., C.K.M., and M.A.A.A. performed experiments; D.H., F.T, S.M., S.D., C.V., P.H.K., J.S., T.G., I.M., C.K.M., and M.A.A.A. analyzed data; D.H., F.T., S.D., J.S., I.M., M.O., C.K.M., S.v.K.R., D.A., J.D., and M.A.A.A. interpreted results of experiments; D.H., F.T., and M.A.A.A. prepared figures; D.H., F.T., and M.A.A.A. drafted manuscript; D.H., F.T., S.D., D.A., W.S., R.S., J.D., and M.A.A.A. edited and revised the manuscript. D.H., F.T., S.M., S.D., C.V., P.H.K.., J.M., R.W., J.S., I.M., M.O., C.M.A., C.K.M., G.P.S., C.P., S.v.K.R., D.A., W.S., R.S., J.D. and M.A.A.A. approved the final version of manuscript.

Corresponding author

Correspondence to Miguel A. Alejandre Alcazar.

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Ethics approval and consent to participate

All animal studies were approved by the local government authorities (LANUV, NRW, Germany; 87–51.04.2010.A372; 84–02.04.2015.A120; 84–02.04.2020.A95).

For macrophage studies, buffy coat from the blood was collected from the hospital blood bank of the University Hospital Cologne (approval No 06.062) or provided by the blood bank of the Universities of Giessen and Marburg Lung Center (AZ 58/15).

BPD and control (non-diseased) lung tissues were obtained through the National Heart, Lung, and Blood Institute LungMAP Consortium Human Tissue Core Biorepository. The biorepository is approved by the University of Rochester Research Subjects Review Board (RSRB00056775). Consent for research use has been provided for each sample. Clinical metadata and histopathology are listed in Table 1.

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Not applicable.

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The authors declare that they have no competing interest.

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Additional file 2.

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Hirani, D.V., Thielen, F., Mansouri, S. et al. CXCL10 deficiency limits macrophage infiltration, preserves lung matrix, and enables lung growth in bronchopulmonary dysplasia. Inflamm Regener 43, 52 (2023). https://doi.org/10.1186/s41232-023-00301-6

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Received: 23 May 2023
Accepted: 10 October 2023
Published: 24 October 2023
DOI: https://doi.org/10.1186/s41232-023-00301-6

CXCL10 deficiency limits macrophage infiltration, preserves lung matrix, and enables lung growth in bronchopulmonary dysplasia

Abstract

Introduction

Results

Transcriptomic analysis identified Cxcl10 as a central hub in hyperoxia-induced inflammation in newborn mice at postnatal day 14 (P14)

Loss of CXCL10 enables alveolar formation, reduces apoptosis, and protects alveolar epithelial type 2 cells (AT2) in newborn mice after hyperoxia

Loss of CXCL10 attenuates fibrotic remodeling in hyperoxia-exposed neonatal lungs through preserved spatial elastic fiber distribution and reduced collagen deposition

Loss of CXCL10 limits macrophage influx into neonatal lungs after hyperoxia

The beneficial effect of CXCL10 deficiency on alveolarization and lung matrix in lungs of neonatal mice exposed to hyperoxia persists after a regeneration phase

Loss of CXCL10 limits macrophage influx into the lung during regeneration from neonatal hyperoxia

Hyperoxia induces Cxcl10 that drives migration of human and murine macrophages through its receptor CXCR3

Macrophage (CD68+) influx with elevated CXCL10 expression in lungs of infants with BPD

Discussion

Conclusion

Material and methods

Sub-analysis of our publicly available RNA sequencing (RNA-Seq) data set

Animal studies and ethical approval

Neonatal hyperoxia-induced lung injury model

Tissue preparation

Quantitative histomorphometric analysis

RNA isolation and quantitative reverse transcriptase PCR (RT-PCR)

Immunoblot

CXCL10 ELISA

Zymography for detection of matrix metalloproteinase 2 (MMP2) and MMP9

TUNEL and SFTPC immunofluorescent staining

Immunohistochemical staining

Picro Sirius-Red staining

Hart’s elastin stain

Semi-quantitative analysis of lung collagen and elastic fiber content

Cell culture experiments

Murine macrophages

Human monocyte-derived macrophages and differentiation

Human M1-like macrophages

M0 macrophages

Macrophage assays and reagents

Migration assay

Reagents

In situ hybridization of human lungs

Statistical analysis

Availability of data and materials

References

Acknowledgements

Funding

Author information

Authors and Affiliations

Contributions

Corresponding author

Ethics declarations

Ethics approval and consent to participate

Consent for publication

Competing interests

Additional information

Publisher’s Note

Supplementary Information

Additional file 1.

Additional file 2.

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About this article

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Keywords

Inflammation and Regeneration

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Macrophage (CD68⁺) influx with elevated CXCL10 expression in lungs of infants with BPD