Skip to main content
Log in

A comparison of human amnion tissue and amnion cells in primary culture by morphological and biochemical criteria

  • Published:
In Vitro Aims and scope Submit manuscript

Summary

Prostaglandins, which are believed to mediate the initiation or maintenance of human labor or both, are synthesized from arachidonic acid. We have shown previously that the arachidonic acid content of two glycerophospholipids (diacyl phosphatidylethanolamine and phosphatidylinositol) in amnion tissue obtained during early labor is decreased compared with that in amnion tissue obtained before labor commenced. We and others have demonstrated that amnion tissue synthesizes prostaglandin E2 from exogenous and endogenous arachidonic acid. Thus, the amnion may be a source of prostaglandins involved in the initiation of parturition. We have investigated whether amnion cells in monolayer culture could be utilized as an in vitro model system for the study of glycerophospholipid and arachidonic acid metabolism in amnion. Several morphological biochemical, and enzymatic characteristics of amnion cells in culture were compared with those of amnion tissue. Morphologically, the amnion cells in culture and amnion tissue are similar. The lipid composition and arachidonic acid content of lipid fractions of amnion cells in culture and of amnion tissue also are similar. The specific activities of phospholipases A2 and C, the enzymes that initiate and thus probably regulate the release of arachidonic acid from phosphatidylethanolamine and phosphatidylinositol, are lower in amnion cells in culture than in amnion tissue obtained from term placentas. The specific activities of diacylglycerol lipase, monoacylglycerol lipase, and diacylglycerol kinase, enzymes that catalyze the release of arachidonic acid from diacylglycerol produced by the action of phospholipase C on phosphatidylinositol, are similar in amnion cells in culture and in amnion tissue. Therefore, we conclude that, based on morphology, lipid composition and enzymatic activities amnion cells in primary culture seem to be an appropriate in vitro model system for the investigation of the regulation of arachidonic acid metabolism in amnion.

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

  1. Zitcer, E. M.; Fogh, J.; Dunnebacke, T. H.: Human amnion cells for large scale production of polio virus. Science 122: 30; 1955.

    Article  PubMed  CAS  Google Scholar 

  2. Gaffney, E. V.; Grimaldi, M. A. Regulation of human amnion cell growth and morphology by sera, plasma and growth factors. Cell Tissue Res. 220: 611–621; 1981.

    Article  PubMed  CAS  Google Scholar 

  3. Dell'Aquila, M. L.; Gaffney, E. V. Growth of normal human amnion epithelial cells in serum-free medium. Exp. Cell Res. 137: 441–446; 1982.

    Article  PubMed  Google Scholar 

  4. Conover, J. H.; Hirschhorm, K. Establishment and genetic stability of human amnion cell lines. Lab. Invest. 24: 38–40; 1971.

    PubMed  CAS  Google Scholar 

  5. Hayflick, L. The establishment of a line (WISH) of human amnion cells in continuous cultivation. Exp. Cell Res. 23: 14–20; 1961.

    Article  PubMed  CAS  Google Scholar 

  6. MacDonald, P. C.; Porter, J. C.; Schwartz, B. E.; Johnston, J. M. Initiation of parturition in the human female. Semin. Perinatol. 2: 273–286; 1978.

    PubMed  CAS  Google Scholar 

  7. Okita, J. R.; MacDonald, P. C.; Johnston, J. M. Mobilization of arachidonic acid from specific glycerophospholipids of human fetal membranes during early labor. J. Biol. Chem. 257: 14029–14034; 1982.

    PubMed  CAS  Google Scholar 

  8. Okazaki, T.; Okita, J. R.; MacDonald, P. C.; Johnston, J. M. Initiation of human parturition. X. Substrate specificity of phospholipase A2 in human fetal membranes. Am. J. Obstet. Gynecol. 130: 432–438; 1978.

    PubMed  CAS  Google Scholar 

  9. Di Renzo, G. C.; Johnston, J. M.; Okazaki, T.; Okita, J. R.; MacDonald, P. C.; Bleasdale, J. E. Phosphatidylinositol-specific phospholipase C in fetal membranes and uterine decidua. J. Clin. Invest. 67: 847–856; 1981.

    Article  PubMed  Google Scholar 

  10. Okazaki, T.; Sagawa, N.; Okita, J. R.; Bleasdale, J. E.; MacDonald, P. C.; Johnston, J. M. Diacylglycerol metabolism and arachidonic acid release in human fetal membranes and decidua vera. J. Biol. Chem. 256: 7316–7321; 1981.

    PubMed  CAS  Google Scholar 

  11. Okazaki, T.; Casey, M. L.; Okita, J. R.; MacDonald, P. C.; Johnston, J. M. Initiation of human parturition. XII. Biosynthesis and metabolism of prostaglandins in human fetal membranes and uterine decidua. Am. J. Obstet. Gynecol. 139: 373–381; 1981.

    PubMed  CAS  Google Scholar 

  12. Humason, G. L. Animal tissue techniques. San Francisco, CA: W. H. Freeman and Company; 1967: 157–159; 306–307.

    Google Scholar 

  13. Pearse, A. G. E. Histochemistry. Boston, MA: Little, Brown and Company; 1968: 460–467.

    Google Scholar 

  14. Rittenhouse-Simmons, S. Indomethacin-induced accumulation of diglyceride in activated human platelets. The role of diglyceride lipase. J. Biol. Chem. 255: 2259–2262; 1980.

    PubMed  CAS  Google Scholar 

  15. Wynn, R. M.; French, G. L. Comparative ultrastructure of the mammalian amnion. Obstet. Gynecol. 31: 759–774; 1968.

    PubMed  CAS  Google Scholar 

  16. Helmy, F. M.; Hack, M. H. Histochemical and lipid studies on human and rat placentas. Am. J. Obstet. Gynecol. 88: 578–583; 1964.

    PubMed  CAS  Google Scholar 

  17. Yoshimura, S.; Nishimura, T.; Yoshida, Y. The morphometry of the Sudan-III-positive granules in the cytoplasm of the human amniotic epithelium. Acta Cytol. (Baltimore) 24: 44–48; 1980.

    CAS  Google Scholar 

  18. McCoshen, J. A.; Chudasama, S.; Tyson, J. E. Differential responsiveness of cells of human amniotic epithelium to ferritin and125I-prolactin in vitro. Placenta Suppl. 3: 33–47; 1981.

    PubMed  CAS  Google Scholar 

  19. McCoshen, J. A.; Tomita, K.; Fernandez, C.; Tyson, J. E. Specific cells of human amnion selectivity localize prolactin. J. Clin. Endocrinol. Metab. 55: 166–169; 1982.

    Article  PubMed  CAS  Google Scholar 

  20. Sagawa, N.; Okazaki, T.; MacDonald, P. C.; Johnston, J. M. Regulation of diacylglycerol metabolism in human amniotic tissue. J. Biol. Chem. 257: 8158–8162; 1982.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

in part, by U.S. Public Health Service Grant 1-T32-HD07190. This investigation was supported in part, by U.S. Public Health Service Grant 5-P50-HD11149 and by a grant-in-aid from the Robert A. Welch Foundation, Houston, Texas.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Okita, J.R., Sagawa, N., Casey, M.L. et al. A comparison of human amnion tissue and amnion cells in primary culture by morphological and biochemical criteria. In Vitro 19, 117–126 (1983). https://doi.org/10.1007/BF02621895

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02621895

Key words

Navigation