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Decrease in lipid levels of syncytiotrophoblast micro-particles reduced their potential to inhibit endothelial cell proliferation

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Abstract

Background

Preeclampsia is characterized by damage to the maternal endothelium that has been suggested to be mediated in part by elevated shedding of inflammatory placental syncytiotrophoblast micro-particles (STBM) into the maternal circulation. Previously, we have shown that STBM, prepared by three different methods: mechanical dissection, in vitro placental explants culture and perfusion of placenta, can inhibit endothelial cell proliferation. Only mechanically prepared STBM induced apoptosis in the endothelial cells. Now, we have examined lipid levels in the three STBM preparations and their differential responses on endothelial cells.

Methods

We examined the lipid levels in the three STBM preparations using thin layer chromatography. Furthermore, the effects of reduced lipid levels in the three STBM preparations using the pharmacological agent methyl-β-cyclodextrin were examined on endothelial cell proliferation and apoptosis.

Results

Among the three STBM preparations, mechanical STBM contained highest levels of lipids. The reduction in lipid levels in mechanical STBM reduced their potential to inhibit human umbilical vein endothelial cells (HUVEC) proliferation and blocked their potential to induce apoptosis. No similar effect was observed following lipid reduction in the two other STBM preparations.

Conclusions

As it has been suggested that mechanically derived STBM may more closely resemble placental micro-particles generated in preeclampsia, our data suggest that lipid content may play a role in the anti-endothelial defects present in this disease.

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Abbreviations

PBS:

Phosphate buffered saline

STBM:

Syncytiotrophoblast micro-particles

MβCD:

Methyl-β-cyclodextrin

HUVEC:

Human umbilical vein endothelial cells

References

  1. Redman CW, Sargent IL (2005) Latest advances in understanding preeclampsia. Science 308:1592–1594

    Article  PubMed  CAS  Google Scholar 

  2. Roberts JM, Cooper DW (2001) Pathogenesis and genetics of pre-eclampsia. Lancet 357:53–56

    Article  PubMed  CAS  Google Scholar 

  3. Redman CW, Sargent IL (2004) Preeclampsia and the systemic inflammatory response. Semin Nephrol 24:565–570

    Article  PubMed  Google Scholar 

  4. Redman CW, Sargent IL (2003) Pre-eclampsia, the placenta and the maternal systemic inflammatory response—a review. Placenta 24(Suppl A):S21–S27

    Article  PubMed  Google Scholar 

  5. Redman CW, Sargent IL (2000) Placental debris, oxidative stress and pre-eclampsia. Placenta 21:597–602

    Article  PubMed  CAS  Google Scholar 

  6. Chua S, Wilkins T, Sargent I, Redman C (1991) Trophoblast deportation in pre-eclamptic pregnancy. Br J Obstet Gynaecol 98:973–979

    PubMed  CAS  Google Scholar 

  7. Huppertz B, Frank HG, Kingdom JC, Reister F, Kaufmann P (1998) Villous cytotrophoblast regulation of the syncytial apoptotic cascade in the human placenta. Histochem Cell Biol 110:495–508

    Article  PubMed  CAS  Google Scholar 

  8. Johansen M, Redman CW, Wilkins T, Sargent IL (1999) Trophoblast deportation in human pregnancy—its relevance for pre-eclampsia. Placenta 20:531–539

    Article  PubMed  CAS  Google Scholar 

  9. Borzychowski AM, Sargent IL, Redman CW (2006) Inflammation and pre-eclampsia. Semin Fetal Neonatal Med 11:309–316

    Article  PubMed  CAS  Google Scholar 

  10. Knight M, Redman CW, Linton EA, Sargent IL (1998) Shedding of syncytiotrophoblast microvilli into the maternal circulation in pre-eclamptic pregnancies. Br J Obstet Gynaecol 105:632–640

    PubMed  CAS  Google Scholar 

  11. Lo YM, Leung TN, Tein MS, Sargent IL, Zhang J, Lau TK, Haines CJ, Redman CW (1999) Quantitative abnormalities of fetal DNA in maternal serum in preeclampsia. Clin Chem 45:184–188

    PubMed  CAS  Google Scholar 

  12. Zhong XY, Laivuori H, Livingston JC, Ylikorkala O, Sibai BM, Holzgreve W, Hahn S (2001) Elevation of both maternal and fetal extracellular circulating deoxyribonucleic acid concentrations in the plasma of pregnant women with preeclampsia. Am J Obstet Gynecol 184:414–419

    Article  PubMed  CAS  Google Scholar 

  13. Hahn S, Holzgreve W (2002) Fetal cells and cell-free fetal DNA in maternal blood: new insights into pre-eclampsia. Hum Reprod Update 8:501–508

    Article  PubMed  CAS  Google Scholar 

  14. Gupta AK, Rusterholz C, Huppertz B, Malek A, Schneider H, Holzgreve W, Hahn S (2005) A comparative study of the effect of three different syncytiotrophoblast micro-particles preparations on endothelial cells. Placenta 26:59–66

    Article  PubMed  CAS  Google Scholar 

  15. Gupta AK, Rusterholz C, Holzgreve W, Hahn S (2005) Syncytiotrophoblast micro-particles do not induce apoptosis in peripheral T lymphocytes, but differ in their activity depending on the mode of preparation. J Reprod Immunol 68:15–26

    Article  PubMed  CAS  Google Scholar 

  16. Var A, Kuscu NK, Koyuncu F, Uyanik BS, Onur E, Yildirim Y, Oruc S (2003) Atherogenic profile in preeclampsia. Arch Gynecol Obstet 268:45–47

    PubMed  CAS  Google Scholar 

  17. Bayhan G, Kocyigit Y, Atamer A, Atamer Y, Akkus Z (2005) Potential atherogenic roles of lipids, lipoprotein(a) and lipid peroxidation in preeclampsia. Gynecol Endocrinol 21:1–6

    Article  PubMed  CAS  Google Scholar 

  18. Belo L, Caslake M, Gaffney D, Santos-Silva A, Pereira-Leite L, Quintanilha A, Rebelo I (2002) Changes in LDL size and HDL concentration in normal and preeclamptic pregnancies. Atherosclerosis 162:425–432

    Article  PubMed  CAS  Google Scholar 

  19. Jaffe EA, Nachman RL, Becker CG, Minick CR (1973) Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria. J Clin Invest 52:2745–2756

    Article  PubMed  CAS  Google Scholar 

  20. Nachman RL, Jaffe EA (2004) Endothelial cell culture: beginnings of modern vascular biology. J Clin Invest 114:1037–1040

    Article  PubMed  CAS  Google Scholar 

  21. Hao M, Mukherjee S, Maxfield FR (2001) Cholesterol depletion induces large scale domain segregation in living cell membranes. Proc Natl Acad Sci USA 98:13072–13077

    Article  PubMed  CAS  Google Scholar 

  22. Thomas JP, Geiger PG, Girotti AW (1993) Lethal damage to endothelial cells by oxidized low density lipoprotein: role of selenoperoxidases in cytoprotection against lipid hydroperoxide- and iron-mediated reactions. J Lipid Res 34:479–490

    PubMed  CAS  Google Scholar 

  23. Huppertz B, Kingdom J, Caniggia I, Desoye G, Black S, Korr H, Kaufmann P (2003) Hypoxia favours necrotic versus apoptotic shedding of placental syncytiotrophoblast into the maternal circulation. Placenta 24:181–190

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

We thank Dr. Sachin Shelke for his kind help in the TLC of STBM. This work was supported in part by a grant from The Special Non-Invasive Advances in Fetal and Neonatal Evaluation Network (SAFE) (No. DMS-2007).

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Correspondence to Anurag Kumar Gupta.

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Gupta, A.K., Holzgreve, W. & Hahn, S. Decrease in lipid levels of syncytiotrophoblast micro-particles reduced their potential to inhibit endothelial cell proliferation. Arch Gynecol Obstet 277, 115–119 (2008). https://doi.org/10.1007/s00404-007-0425-2

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  • DOI: https://doi.org/10.1007/s00404-007-0425-2

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