open access

Vol 91, No 6 (2020)
Research paper
Published online: 2020-06-30
Get Citation

Expression of CD44 and IL-10 in normotensive and preeclamptic placental tissue

Mehmet Obut1, Süleyman Cemil Oğlak1
·
Pubmed: 32627155
·
Ginekol Pol 2020;91(6):334-341.
Affiliations
  1. Department of Perinatology, Ministry of Health, Ankara City Hospital, Ankara, Turkey

open access

Vol 91, No 6 (2020)
ORIGINAL PAPERS Obstetrics
Published online: 2020-06-30

Abstract

Objectives: We aimed to demonstrate cell-cell adhesion and apoptotic changes in preeclamptic placentas by examining the expression of CD44 and IL-10. Material and methods: Placenta samples of 15 preeclamptic and 15 healthy 35–38th week-pregnant women were involved in the study. Tissue samples were taken only from the maternal side of the placenta and fixed in 10% formaldehyde, then blocked in paraffin wax and 5 μm-thick sections were cut and stained with Masson Trichrome. Antigen retrieval was performed for sections, incubated with CD44 antibody and anti-IL-10 antibody. After the application of streptavidin peroxidase followed by AEC chromogen solution, sections were counterstained with Mayer hematoxylin. Results: In the preeclampsia group, increased CD44 positive expression was observed in maternal decidua cells and fibroblast cells close to root villi. CD44 was positively expressed in muscle cells around the blood vessels, mucosal connective tissue areas, syncytial nodes, and syncytial bridges. In the preeclampsia group, significant increased IL-10 expression was seen in subendothelial layers of the medium-sized vessels in the maternal region. IL-10 was also positively expressed in decidua cells outside the vessels, and inflamed connective tissue areas, chorionic villus cells with intense inflammation in intervillous spaces. Conclusions: CD44 was found to be an essential molecule in the regulation of vascular permeability, inflammatory response, activation of the cells, cell-to-cell interaction, and the signaling pathways to which they are associated. Since IL-10 regulates appropriate pregnancy outcomes and contributes to the balance of anti-inflammatory signals via both paracrine and autocrine regulators of trophoblast activity, we proposed that it might be a key to elucidate the etiology of preeclampsia with CD44 receptor.

Abstract

Objectives: We aimed to demonstrate cell-cell adhesion and apoptotic changes in preeclamptic placentas by examining the expression of CD44 and IL-10. Material and methods: Placenta samples of 15 preeclamptic and 15 healthy 35–38th week-pregnant women were involved in the study. Tissue samples were taken only from the maternal side of the placenta and fixed in 10% formaldehyde, then blocked in paraffin wax and 5 μm-thick sections were cut and stained with Masson Trichrome. Antigen retrieval was performed for sections, incubated with CD44 antibody and anti-IL-10 antibody. After the application of streptavidin peroxidase followed by AEC chromogen solution, sections were counterstained with Mayer hematoxylin. Results: In the preeclampsia group, increased CD44 positive expression was observed in maternal decidua cells and fibroblast cells close to root villi. CD44 was positively expressed in muscle cells around the blood vessels, mucosal connective tissue areas, syncytial nodes, and syncytial bridges. In the preeclampsia group, significant increased IL-10 expression was seen in subendothelial layers of the medium-sized vessels in the maternal region. IL-10 was also positively expressed in decidua cells outside the vessels, and inflamed connective tissue areas, chorionic villus cells with intense inflammation in intervillous spaces. Conclusions: CD44 was found to be an essential molecule in the regulation of vascular permeability, inflammatory response, activation of the cells, cell-to-cell interaction, and the signaling pathways to which they are associated. Since IL-10 regulates appropriate pregnancy outcomes and contributes to the balance of anti-inflammatory signals via both paracrine and autocrine regulators of trophoblast activity, we proposed that it might be a key to elucidate the etiology of preeclampsia with CD44 receptor.

Get Citation

Keywords

CD44; IL-10; normotensive and preeclampsia; placenta

About this article
Title

Expression of CD44 and IL-10 in normotensive and preeclamptic placental tissue

Journal

Ginekologia Polska

Issue

Vol 91, No 6 (2020)

Article type

Research paper

Pages

334-341

Published online

2020-06-30

Page views

1752

Article views/downloads

1203

DOI

10.5603/GP.2020.0058

Pubmed

32627155

Bibliographic record

Ginekol Pol 2020;91(6):334-341.

Keywords

CD44
IL-10
normotensive and preeclampsia
placenta

Authors

Mehmet Obut
Süleyman Cemil Oğlak

References (34)
  1. Brown HL, Small MJ. Overview of maternal mortality and morbidity updated: Jan 2018. Erişim: 13 Mart 2018.
  2. Patel A, Dash PR. Formation of atypical podosomes in extravillous trophoblasts regulates extracellular matrix degradation. Eur J Cell Biol. 2012; 91(3): 171–179.
  3. Lyall F, Robson SC, Bulmer JN. Spiral artery remodeling and trophoblast invasion in preeclampsia and fetal growth restriction: relationship to clinical outcome. Hypertension. 2013; 62(6): 1046–1054.
  4. Chaiworapongsa T, Chaemsaithong P, Yeo L, et al. Pre-eclampsia part 1: current understanding of its pathophysiology. Nat Rev Nephrol. 2014; 10(8): 466–480.
  5. Gathiram P, Moodley J. Pre-eclampsia: its pathogenesis and pathophysiolgy. Cardiovasc J Afr. 2016; 27(2): 71–78.
  6. Madazli R, Budak E, Calay Z, et al. Correlation between placental bed biopsy findings, vascular cell adhesion molecule and fibronectin levels in pre-eclampsia. BJOG. 2000; 107(4): 514–518.
  7. Toole B. Hyaluronan: from extracellular glue to pericellular cue. Nature Reviews Cancer. 2004; 4(7): 528–539.
  8. Vikesaa J, Hansen TVO, Jønson L, et al. RNA-binding IMPs promote cell adhesion and invadopodia formation. EMBO J. 2006; 25(7): 1456–1468.
  9. Roth I, Corry DB, Locksley RM, et al. FisherHuman placental cytotrophoblasts produce the immunosuppressive cytokine interleukin. J Exp Med. 1996; 184: 539–548.
  10. HEIKKINEN J, MOTTONEN M, KOMI J, et al. Phenotypic characterization of human decidual macrophages. Clin Exp Immunol. 2003; 131(3): 498–505.
  11. Lidstrom C, Matthiesen L, Berg G, et al. Cytokine secretion patterns of NK cells and macrophages in early human pregnancy decidua and blood: implications for suppressor macrophages in decidua . Am J Reprod Immunol. 2003; 50: 444–452.
  12. Hanna N, Hanna I, Hleb M, et al. Gestational age-dependent expression of IL-10 and its receptor in human placental tissues and isolated cytotrophoblasts. J Immunol. 2000; 164: 5721–5728.
  13. Chaouat G, Cayol V, Mairovitz V, et al. Localization of the Th2 cytokines IL-3, IL-4, IL-10 at the fetomaternal interface during human and murine pregnancy and lack of requirement for Fas/Fas ligand interaction for a successful allogeneic pregnancy. Am J Reprod Immunol. 1999; 42: 1–13.
  14. American College of Obstetricians and Gynecologists. Hypertension in Pregnancy. Obstet Gynecol. 2013; 122: 1122–1131.
  15. Steegers E, Dadelszen Pv, Duvekot J, et al. Pre-eclampsia. Lancet. 2010; 376(9741): 631–644.
  16. Şencan İ, Engin-Üstün Y, Sanisoğlu S. 2014 yılı Türkiye ulusal anne ölümlerinin demografi k verilere göre değerlendirilmesi. J Gynecol Obstet Neonatal. 2016; 13: 45.
  17. Peres GM, Mariana M, Cairrão E. Pre-Eclampsia and Eclampsia: An Update on the Pharmacological Treatment Applied in Portugal. J Cardiovasc Dev Dis. 2018; 5(1).
  18. Sava RI, March KL, Pepine CJ. Hypertension in pregnancy: Taking cues from pathophysiology for clinical practice. Clin Cardiol. 2018; 41(2): 220–227.
  19. Çelik N, Saruhan A. Gebelikte riskli durumlar. In: Sevil Ü, Ertem G. ed. Perinataloji ve bakım. Ankara Nobel Tıp Kitabevleri, Ankara 2016: 231–246.
  20. Walentin K, Hinze C, Schmidt-Ott KM. The basal chorionic trophoblast cell layer: An emerging coordinator of placenta development. Bioessays. 2016; 38(3): 254–265.
  21. Chaiworapongsa T, Chaemsaithong P, Yeo L, et al. Pre-eclampsia part 1: current understanding of its pathophysiology. Nat Rev Nephrol. 2014; 10(8): 466–480.
  22. Balsak D, Togrul C, Ekinci C, et al. Severe pre-eclampsia complicated by HELLP syndrome alterations in the structure of the umbilical cord (morphometric and immunohistochemical study). Biotechnol Biotechnol Equip. 2015; 29(2): 345–350.
  23. Zhu R, Wang SC, Sun C, et al. Hyaluronan-CD44 interaction promotes growth of decidual stromal cells in human first-trimester pregnancy. PLoS One. 2013; 8(9): e74812.
  24. Jacques S, Dadi H, Letarte M. CD44 in human placenta: Localization and binding to hyaluronic acid. Placenta. 1993; 14(1): 25–39.
  25. Thapa R, Wilson GD. The Importance of CD44 as a Stem Cell Biomarker and Therapeutic Target in Cancer. Stem Cells Int. 2016; 2016: 2087204.
  26. Mambetsariev N, Mirzapoiazova T, Mambetsariev B, et al. Hyaluronic Acid binding protein 2 is a novel regulator of vascular integrity. Arterioscler Thromb Vasc Biol. 2010; 30(3): 483–490.
  27. Singleton PA, Dudek SM, Ma SF, et al. Transactivation of sphingosine 1-phosphate receptors is essential for vascular barrier regulation. Novel role for hyaluronan and CD44 receptor family. J Biol Chem. 2006; 281(45): 34381–34393.
  28. Ziganshina MM, Pavlovich SV, Bovin NV, et al. Hyaluronic Acid in Vascular and Immune Homeostasis during Normal Pregnancy and Preeclampsia. Acta Naturae. 2016; 8(3): 59–71.
  29. Lesley J, Hyman R, Kincade PW. CD44 and its interaction with extracellular matrix. Adv Immunol. 1993; 54: 271–335.
  30. Bowen JM, Chamley L, Mitchell MD, et al. Cytokines of the placenta and extra-placental membranes: biosynthesis, secretion and roles in establishment of pregnancy in women. Placenta. 2002; 23(4): 239–256.
  31. Thaxton JE, Sharma S. Interleukin-10: a multi-faceted agent of pregnancy. Am J Reprod Immunol. 2010; 63(6): 482–491.
  32. Chatterjee P, Chiasson VL, Bounds KR, et al. Regulation of the anti-inflammatory cytokines interleukin-4 and interleukin-10 during pregnancy. Frontiers in Immunology |Inflammation. 2014; 5: Article 253.
  33. Hennessy A, Pilmore HL, Simmons LA, et al. A deficiency of placental IL-10 in preeclampsia. J Immunol. 1999; 163(6): 3491–3495.
  34. Wilczyński JR, Tchórzewski H, Głowacka E, et al. Cytokine secretion by decidual lymphocytes in transient hypertension of pregnancy and pre-eclampsia. Mediators Inflamm. 2002; 11(2): 105–111.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp. z o.o., ul. Świętokrzyska 73, 80–180 Gdańsk
tel.:+48 58 320 94 94, faks:+48 58 320 94 60, e-mail:  viamedica@viamedica.pl