Mechanism of SCD Participation in Lipid Droplet-Mediated Steroidogenesis in Goose Granulosa Cells

Abstract

Stearoyl-CoA desaturase (SCD) is a key enzyme catalyzing the rate-limiting step in monounsaturated fatty acids (MUFAs) production. There may be a mechanism by which SCD is involved in lipid metabolism, which is assumed to be essential for goose follicular development. For this reason, a cellular model of SCD function in goose granulosa cells (GCs) via SCD overexpression and knockdown was used to determine the role of SCD in GC proliferation using flow cytometry. We found that SCD overexpression induced and SCD knockdown inhibited GCs proliferation. Furthermore, ELISA analysis showed that SCD overexpression increased the total cholesterol (TC), progesterone, and estrogen levels in GCs, while SCD knockdown decreased TC, progesterone, and estrogen levels (p < 0.05). Combining these results with those of related multi-omics reports, we proposed a mechanism of SCD regulating the key lipids and differentially expressed gene (DEGs) in glycerophospholipid and glycerolipid metabolism, which participate in steroidogenesis mediated by the lipid droplet deposition in goose GCs. These results add further insights into understanding the lipid metabolism mechanism of goose GCs.

1. Introduction

Recent research has revealed the significant role of stearoyl-CoA desaturase (SCD) in lipid metabolism in vivo [1,2]. SCD is a pivotal lipogenic enzyme predominantly located in the endoplasmic reticulum (ER). It converts saturated long-chain fatty acids (SFAs) into monounsaturated fatty acids (MUFAs) and is the rate-limiting enzyme in MUFA biosynthesis in vivo [3]. The resulting MUFAs are major components of triglycerides, cholesterol esters, and phospholipids [4,5,6,7]. In addition to being lipid components, MUFAs may also serve as mediators of signal transduction, cellular differentiation, and apoptosis [8,9]. Alteration in SCD expression alters the fatty acid profile of these lipids, yielding diverse effects on cellular function. High SCD activity and alteration in the balance between saturated and monounsaturated fatty acids are implicated in various diseases, including cancer, diabetes, atherosclerosis, and obesity [8,10].

Lipid droplets (LDs) are fat-storing organelles comprising a hydrophobic core of triacylglycerols (TAGs) and cholesterol esters surrounded by a phospholipid monolayer with various embedded proteins [11,12]. Accumulation of LDs in the cytoplasm plays a vital role in energy balance, membrane synthesis, and cell signal transduction. The turnover of LDs (e.g., through hydrolysis) can transfer hormone synthesis precursors, release lipid components for membrane synthesis, and secrete signaling molecules as lipid mediators [13]. Steroidogenic cells of the adrenal cortex, testes, and ovaries contain tiny LDs that primarily store cholesterol esters and serve as a reservoir of cholesterol for the synthesis and maintenance of membranes [14,15]. Although all animal cells package and store neutral lipids as discrete intracellular storage droplets, there is little information on the molecular processes that govern the deposition or catabolism of stored lipid components.

Indigenous Tianfu goose (Anas cygnoides) are commercially important farm animals in southern China. However, their poor egg-laying performance hinders their industrial application [16]. Many growing follicles undergo atresia as they advance toward ovulation. Numerous factors are involved in goose follicle maturation, and little attention has been paid to lipid metabolism in granulosa cells (GCs). In our previous research, we confirmed for the first time that de novo lipogenesis occurs in goose GCs [17]. Furthermore, SCD overexpression enhanced the intracellular level of cholesterol esters, particularly CE (20:4), which facilitates the synthesis and subsequent esterification of cholesterol into LDs in goose GCs [18]. While studies have demonstrated that SCD is an important rate-limiting enzyme in lipid metabolism, research on goose follicular steroidogenesis is lacking. Therefore, this study explored the effect of SCD on cell proliferation as well as total cholesterol (TC), estrogen, and progesterone levels in Tianfu goose GCs. Thus, we aim to deepen our understanding of the mechanisms of SCD in lipid metabolism during goose GC follicle development.

2. Materials and Methods

2.1. Animals and Granulosa Layer Isolation

A maternal line of Tianfu geese was raised under natural temperature and light conditions at the waterfowl breeding experimental station at Sichuan Agricultural University. For granulosa layer isolation, six geese showing regular laying schedules were randomly selected and sacrificed 2 h after oviposition via post-anesthesia exsanguination. A pool of hierarchical follicles was immediately collected from six goose abdominal cavities and placed in sterile normal saline. The outer connective tissue was removed from the follicles, and follicles were bisected to allow the yolk and adherent granulosa layer to flow out. GCs were isolated as previously described [19]. All experimental procedures involving animal manipulation were approved by the Committee of the School of Farm Animal Genetic Resources Exploration and Innovation Key Laboratory, College of Animal Science and Technology, Sichuan Agricultural University, under permit no. DKY20170913 and were performed in accordance with the Regulations of the Administration of Affairs Concerning Experimental Animals (China 1988). All efforts were made to minimize animal suffering in accordance with the requirements of the Beijing Animal Welfare Committee.

2.2. Primary Cell Culture and Transfection

The granulosa layer was dispersed by incubation in 0.1% type II collagenase (Sigma-Aldrich, Burlington, MA, USA) for 10 min in a 37 °C water bath. After centrifugation, the GCs were dispersed and pelleted by centrifugation at 1000× g for 10 min. Then, the supernatant was discarded, and GCs were resuspended in 3 mL of fresh basic medium without collagenase and centrifuged. The washing procedure was repeated twice. The GCs were dispersed in DMEM supplemented with 1% antibiotic/antimycotic solution (Solarbio, Beijing, China) and 3% fetal bovine serum (Gibco, Waltham, MA, USA). The viability of GCs was always greater than 90% and incubated in a water-saturated atmosphere of 95% air and 5% CO₂ at 37 °C in an incubator (Thermo, Waltham, MA, USA). Transient transfections based on the GCs cellular model of SCD function (SCD-specific overexpression and knockdown) were performed using Lipofectamine^® 3000 and Lipofectamine™ RNAiMAX Transfection Reagent (Invitrogen, Waltham, MA, USA), according to the manufacturer’s protocol. SCD-specific overexpression was used to achieve SCD mRNA overexpression, termed pEGFP-N1/SCD, and the pEGFP-N1/empty vector (GFP vector) served as the negative control. Another control with no transfection components was also included. Specific small interfering RNA (SCD siRNA-210 and siRNA-405) were used to achieve SCD mRNA knockdown, with scrambled siRNA as a negative control. The primers of pEGFP-N1/SCD and the sequences of the siRNAs were determined as previously described [18,20].

2.3. Cell Proliferation Assay

The effect of SCD overexpression and SCD knockdown on the cell cycle stages of GCs was analyzed using an Accuri C6 flow cytometer (BD Biosciences, San Jose, CA, USA) with PI/RNase staining buffer (BD Biosciences). Briefly, 1 × 10⁵ cells were incubated overnight in 6-well plates. After 48 h transfection treatment, the cells were washed once with phosphate-buffered saline (PBS) solution and collected by centrifugation at 250× g for 5 min. Cells were then resuspended in 75% cold ethanol at −20 °C for 24 h. Before flow cytometry analysis, cells were washed with PBS and mixed with PI/RNase staining buffer for 30 min. Finally, the data were analyzed using ModFit software (Ashland, OR, USA). The cell proliferative index (PI) was calculated according to the following formula: PI (%) = (S + G2/M)/(G0/G + S+G2/M) × 100%, as described previously [21].

2.4. Measuring TC, Progesterone, and Estrogen Levels

After SCD overexpression and SCD knockdown in GCs, changes in the intracellular and extracellular cholesterol, estrogen, and progesterone levels were measured using the Goose TC ELISA Kit, Goose Progesterone ELISA Kit, and Goose estrogen (E) ELISA Kit (NJJCBIO, Nanjing, China), respectively. Each cell and culture medium was diluted five times with sample diluent, and 50 µL of the resultant dilution was added to the enzyme label plate. Plates were incubated at 37 °C for 30 min, washed five times with wash buffer, and air-dried at room temperature. A standard reagent (50 µL) was added to the plates, which were then washed five times. Next, 50 µL each of reagents A and B were added to the plates, which were incubated at 37 °C in the dark for 10 min. Finally, a 50 µL stop buffer was added, and the optical density (OD) value was measured using an automatic enzyme immunoassay analyzer at 450 nm.

2.5. Statistical Analysis

The experiment was repeated three times, and multiple means were compared using independent t-tests in the SPSS 19.0 statistical software (SPSS Inc., Chicago, IL, USA). All data are expressed as mean ± SD, and significance was assumed at p < 0.05. All data were visualized using GraphPad Prism 6.01 (GraphPad Software, San Diego, CA, USA).

3. Results

3.1. Effect of SCD Regulated Cell Cycle and Proliferation of Goose GCs

We used PI/RNase staining buffer to assess the goose GCs cell cycle after SCD overexpression and SCD knockdown (Figure 1). The results showed that after SCD overexpression, the proportion of GCs in the S phase was lower. The PI of GCs in the SCD overexpression group was markedly higher than that of the control or GFP groups (

Table 1. Cell cycle results detected by flow cytometry.

Group	G0/G1 (%)	G2/M (%)	S (%)	PI (%)
Control	67.21	2.15	29.64	0.32
GFP	62.41	3.02	34.57	0.38
GFP-SCD	51.49	3.74	44.76	0.49
Scramble	52.51	1.91	45.58	0.48
SiRNA-210	69.99	2.28	27.73	0.30
SiRNA-405	60.99	2.44	36.57	0.39

). We further conducted SCD knockdown studies as shown in Table 1. Compared with the scramble group, the S cells to PI ratio markedly decreased in both the siRNA-210 and siRNA-405 groups.

3.2. SCD Regulated TC Content of Goose GCs

The production of TC content in the supernatant culture medium and cells was determined using ELISA. SCD overexpression led to significantly (p < 0.05) increased TC content in the culture medium. Additionally, the SCD overexpression group had higher TC content than the control and GFP groups (Figure 2A). In addition, compared with the scramble group, the TC content in the culture medium showed a post-transfection decrease in the siRNA-405 group; however, the siRNA-405 group revealed a contrasting trend. Meanwhile, SCD knockdown decreased TC content in the cells, among which the siRNA-210 group showed significantly (p < 0.05) decreased TC content in the cells (Figure 2B).

3.3. SCD Regulated Progesterone and Estrogen Secretion of Goose GCs

We also investigated the effects of SCD overexpression and SCD knockdown on progesterone and estrogen secretion in goose GCs using ELISA. Compared with the control and GFP groups, SCD overexpression significantly (p < 0.05) increased progesterone secretion in the culture medium and cells (Figure 3A). Meanwhile, compared with the scramble group, progesterone secretion in the culture medium and cells decreased after SCD knockdown; among them, the siRNA-210 group significantly (p < 0.05) decreased progesterone secretion in the cells (Figure 3B). In addition, SCD overexpression increased estrogen secretion in the culture medium and significantly increased estrogen secretion in cells (Figure 3C). SCD knockdown decreased estrogen secretion in the culture medium and cells (Figure 3D).

4. Discussion

In the present study, we used a GC model of SCD function to obtain new evidence that SCD participates in GC proliferation and steroidogenesis. We demonstrated that SCD overexpression induced GC proliferation, whereas SCD knockdown inhibited GC proliferation (Table 1). SCD is the rate-limiting enzyme in the biosynthesis of monounsaturated fatty acids from saturated fatty acids, and accumulating evidence suggests SCD is a target for growth factors related to cell growth [22,23]. Notably, most cancer cells contain a high SCD activity to demand an even higher particular lipogenesis to support the rapid growth and de novo synthesis of membranes [8,24]. In our previous report, we investigated the metabolic mechanism of SCD during goose follicular development, among lipid metabolism-related pathways, LC-MS/MS analysis revealed the critical role of the steroid hormone biosynthesis/steroid biosynthesis pathway [20]. In this study, we confirmed that SCD overexpression increases TC content, and SCD knockdown decreases TC content in goose GCs, as evidenced by ELISA (Figure 2). The presence of normal MUFA levels would maintain a more appropriate ratio of cholesterol to other lipids, helping maintain cell membrane integrity [25]. Excess-free cholesterol has been known to lead to cell death [26]. It is tempting to speculate that TC content in the supernatant culture medium was higher than that in the cells, probably due to an increase in the amount of cellular free cholesterol secreted by cells. In addition, SCD is a resident ER protein; recent data show that an excess of SFAs and cholesterol disrupts lipid homeostasis in the ER membrane and induces ER stress, resulting in cell apoptosis and death [27]. Overall, these studies suggest that SCD activity and the availability of MUFAs correlate with malignant cell survival and proliferation [28,29].

Increasing evidence has shown the importance of lipid metabolism in goose follicle development [30,31]; we also demonstrated that de novo lipogenesis occurs in goose GCs [17], revealing that the LD accumulation capacity of goose GCs depends on the different stages of follicle development, with the highest accumulation capacity during the preovulatory follicle stage [32]. The accumulation of LDs in the cytoplasm plays a key role in the energy balance, membrane synthesis, and cell signal transduction [33,34]. In addition, SCD also plays a crucial role in lipid metabolism [35,36]; however, a causal relationship between the function of SCD and goose follicle development has not yet been well established. Further lipidomic profiling research on the LD accumulation capacity and abundance regulated by SCD in goose GCs identified that altered SCD expression affects LD content and changes lipid classes [18]. We speculate that endogenous LDs are a source of energy for steroidogenesis and proliferation in GCs and confirmed that SCD overexpression increases progesterone and estrogen secretion. Conversely, SCD knockdown decreases progesterone and estrogen secretion in goose GCs (Figure 3). Most other types of steroidogenic cells, such as those of the adrenal cortex, testes, and ovaries, contain tiny LDs that primarily store cholesterol esters and use them as substrates for steroid hormone synthesis [37,38]. We also confirmed that SCD overexpression results in increased esterification of cholesterol in goose GCs [20]. Similar studies have been confirmed in mice Chinese hamster ovary cells [39], whose results demonstrate that SCD expression is required to generate MUFAs as the preferred substrates for cholesterol ester synthesis.

Although goose GCs store neutral lipids in LDs, there is little information on the molecular processes governing the deposition or catabolism of stored lipid components. Evidence indicates that SCD might be the pivotal control point regulating hepatic lipogenesis and lipid oxidation. SCD deficiency decreases the transcription of lipogenic genes, down-regulates de novo fatty acid synthesis, and increases the β-oxidation rate [40]. Consistent results were also confirmed in adipose tissues [41]. SCD deficient mice are characterized by a reduction in the percentage of fatty acids comprising MUFA, thereby significantly decreasing the synthesis of neutral lipids, such as triglycerides and cholesterol esters [39,42]. Even when the diet was supplemented with high levels of MUFA, decreasing SCD activity seemingly decreased lipid accumulation by limiting the supply of endogenously synthesized MUFAs [43]. There is ample evidence indicating that SCD can influence the partitioning of fatty acids into and out of neutral lipid species, which is essential in lipid metabolism and body weight control [44,45]. SCD is emerging as a potential therapeutic target for treating obesity, diabetes, and other metabolic diseases [46,47]. Lipid metabolism is highly regulated and complex; therefore, previous studies applied a multi-omics approach to analyze the changes in specific genes, metabolites, and lipid classes associated with SCD overexpression and SCD knockdown in goose GCs [18,20]. Combined with these studies, Figure 4 illustrates a potential mechanism of SCD-mediated regulation of key lipids as well as DEG of glycerophospholipid and glycerolipid metabolic pathways, participating in steroidogenesis and proliferation mediated by LD deposition in goose GCs.

5. Conclusions

In summary, our findings point to the vital role of SCD expression in mediating proliferation and steroidogenesis in goose GCs. These understandings should shed light on providing a new direction for exploring the mechanisms of lipid metabolism in goose follicle development.