Immunohistochemical localization of podoplanin in the placentas of HIV-positive preeclamptic women

Turk J Med Sci. 2018 Oct 31;48(5):916-924. doi: 10.3906/sag-1706-88.

Abstract

Background/aim: Impaired lymphatic function is associated with pathological conditions. The presence of placental lymphatics is still under debate. This study evaluates the placental podoplanin expression in normotensive and preeclamptic women with and without HIV. Materials and methods: Normotensive (n = 60) and preeclamptic (n = 120) pregnant women were stratified into early and late onset preeclampsia and further divided by HIV status. Immunostaining was performed using the podoplanin antibody prior to the morphometric image analysis. Results: Podoplanin was immunolocalized in a reticular-like stroma complex within the exchange and conducting villi. The immunoexpression of podoplanin was significantly upregulated in the exchange villi (P = 0.001) irrespective of the pregnancy type and HIV status. Based on pregnancy type, podoplanin was downregulated in early onset preeclampsia (15.33 ± 4.27%) compared to late onset preeclampsia in the exchange villi (17.85 ± 4.74%; P = 0.04). Podoplanin was upregulated in HIV+ vs. HIV- cases regardless of pregnancy and villi type. Irrespective of pregnancy type, podoplanin immunoexpression within exchange villi was different (P = 0.008) between the HIV+ and HIV- groups. Conclusion: Placental fluid homeostasis is maintained by a podoplanin reticular-like complex within conducting and exchange villi, being upregulated in HIV-positive pregnancies.

Keywords: Podoplanin; HIV infection; preeclampsia; pregnancy.

MeSH terms

  • Adult
  • Female
  • HIV Infections / complications*
  • Humans
  • Immunohistochemistry
  • Membrane Glycoproteins* / analysis
  • Membrane Glycoproteins* / chemistry
  • Membrane Glycoproteins* / metabolism
  • Placenta / chemistry*
  • Placenta / metabolism
  • Pre-Eclampsia / metabolism*
  • Pregnancy
  • Pregnancy Complications, Infectious / metabolism*
  • Young Adult

Substances

  • Membrane Glycoproteins
  • PDPN protein, human