Skip to main content
Log in

A comparison of two populations of decidual cells by immunocytochemistry and prostaglandin production

  • Published:
Histochemistry Aims and scope Submit manuscript

Summary

The decidua has been implicated in the control of human labour, particularly through changes in prostaglandin production, but this tissue contains a number of different cell types. A density gradient system was used to obtain two populations of cells from term human decidua, and these populations were characterised. The more dense cells (population B) was a mixed population, predominantly macrophages (80%), but small numbers of T- and B-lymphocytes were also present, as identified by immunocytochemistry. Most of these cell types also contained detectable levels of cyclooxygenase enzyme. The less-dense cell population (population A) did not contain significant numbers of the above cell types and released prolactin, suggesting that they were decidual stromal cells. This preparation of decidual stromal cells may be of use in defining the functions of these cells in labour.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ashboth G, Gimes G, Hertelendy F, Toth M (1989) The relation between thromboxane and prostaglandin synthesis in human decidua tissues: a comparison of eicosanoid synthesis in minced tissue with that in a cell-free preparation. Biochim Biophys Acta 1002:101–108

    Google Scholar 

  • Bennett PR, Chamberlain GVP, Patel L, Elder MG, Myatt L (1990) Mechanisms of parturition: the transfer of prostaglandin E2 and 5-hydroxy-eicosatetraenoic acid across fetal membranes. Am J Obstet Gynecol 162:683–687

    Google Scholar 

  • Bleasdale JE, Johnston JM (1984) Prostaglandins and human parturition: regulation of arachidonic acid mobilization. Rev Perinat Med 5:151–191

    Google Scholar 

  • Bryant-Greenwood GD, Rees MCP, Turnbull AC (1987) Immunocytochemical localisation of relaxin, prolactin and prostaglandin synthase in human amnion, chorion and decidua. J Endocrinol 114:491–496

    Google Scholar 

  • Bulmer JN, Pace D, Ritson A (1988) Immunoregulatory cells in human decidua: morphology, immunocytochemistry and function. Reprod Nutr Dev 28:1599–1614

    Google Scholar 

  • Bygdeman M, Kwon SU, Mukherjee T, Wiqvist N (1968) Effect of intravenous infusion of prostaglandin E1 and E2 on motility of the pregnant human uterus. Am J Obstet Gynecol 102:317–326

    Google Scholar 

  • Bygdeman M (1984) The use of prostaglandins and their analogues for abortion. Clin Obstet Gynecol 11:573–584

    Google Scholar 

  • Casey ML, MacDonald PC (1986) The initiation of labour in women: regulation of phospholipid and arachidonic acid metabolism and of prostaglandin production. Semin Perinatol 10:270–275

    Google Scholar 

  • Casey ML, MacDonald PC (1988) Biomolecular processes in the initiation of parturation: decidual activation. Clin Obstet Gynecol 31:533–552

    Google Scholar 

  • Casey ML, Cox SM, Beutler B, Milewich L, MacDonald PC (1989) Cachetin/tumor necrosis factor-α formation in human decidua. J Clin Invest 83:430–436

    Google Scholar 

  • Dray F, Frydman R (1975) Primary prostaglandins in amniotic fluid in pregnancy and spontaneous labour. Am J Obstet Gynecol 126:13–19

    Google Scholar 

  • Gery I, Waksman BH (1972) Potentiation of the T-lymphocyte response to mitogens. II. The cellular source of potentiating mediator(s). J Exp Med 136:143–155

    Google Scholar 

  • Healy DL, Kimpton WG, Muller HK, Burger HG (1979) The synthesis of immunoreactive prolactin by decidua-chorion. Br J Obstet Gynaecol 86:307–313

    Google Scholar 

  • Hoshina M, Boothby M, Boime I (1982) Cytological localization of chorionic gonadotropin α and placental lactogen mRNAs during development of human placenta. J Cell Biol 93:190–198

    Google Scholar 

  • Karim SMM, Hillier K, Trussell RR, Patel RC, Tamusange S (1970) Induction of labour with prostaglandin E2. J Obstet Gynaecol Br Commonw 77:200–210

    Google Scholar 

  • Keirse MJNC, Turnbull AC (1976) The fetal membranes as a possible source of amniotic fluid prostaglandins. Br J Obstet Gynaecol 83:146–151

    Google Scholar 

  • Matsui S, Yoshimura N, Oka T (1989) Characterization and analysis of soluble suppressor factor from early human decidual cells. Transplantation 47:678–683

    Google Scholar 

  • Nakla S, Skinner K, Mitchell BF, Challis JRG (1986) Changes in prostaglandin transfer across human fetal membranes obtained after spontaneous labor. Am J Obstet Gynecol 155:1337–1341

    Google Scholar 

  • Okazaki T, Casey ML, Okita JR, MacDonald PC, Johnston JM (1981) Initiation of human parturition. XII: Biosynthesis and metabolism of prostaglandins in human fetal membranes and uterine decidua. Am J Obstet Gynecol 139:373–381

    Google Scholar 

  • Price TM, Kauma SW, Curry TE, Clark MR (1989) Immunohistochemical localization of prostaglandin endoperoxide synthase in human fetal membranes and decidua. Biol Reprod 41:701–705

    Google Scholar 

  • Riddick DH, Luciano AA, Kusmik WF, Maslar IA (1978) De novo synthesis of prolactin by human decidua. Life Sci 23:1913–1922

    Google Scholar 

  • Roseblade CK, Sullivan MHF, Khan H, Lumb MR, Elder MG (1990) Limited transfer of prostaglandin E2 across the fetal membranes before and after labour. Acta Obstet Gynecol Scand 69:399–403

    Google Scholar 

  • Starkey PM, Sargent IL, Redman CWG (1988) Cell populations in human early pregnancy decidua: characterization and isolation of large granular lymphocytes by flow cytometry. Immunology 65:129–134

    Google Scholar 

  • Vince GS, Starkey PM, Jackson MC, Sargent IL, Redman CWG (1990) Flow cytometric characterisation of cell populations in human pregnancy decidua and isolation of decidual macrophages. J Immunol Methods 132:181–189

    Google Scholar 

  • Warrick C, Skinner K, Mitchell BF, Challis JRG (1985) Relation between cyclic adenosine monophosphate and prostaglandin output by dispersed cells from human amnion and decidua. Am J Obstet Gynecol 153:66–71

    Google Scholar 

  • Wilson T, Liggins GC, Whittaker DJ (1988) Oxytocin stimulates the release of arachidonic acid and prostaglandin F from human decidual cells. Prostaglandins 35:771–780

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Khan, H., Ishihara, O., Elder, M.G. et al. A comparison of two populations of decidual cells by immunocytochemistry and prostaglandin production. Histochemistry 96, 149–152 (1991). https://doi.org/10.1007/BF00315985

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00315985

Keywords

Navigation