Role of Slit2/Robo1 in trophoblast invasion and vascular remodeling during ectopic tubal pregnancy

Placenta. 2015 Oct;36(10):1087-94. doi: 10.1016/j.placenta.2015.08.002. Epub 2015 Aug 10.

Abstract

Introduction: For ectopic tubal pregnancy to be viable, it requires a supporting vascular network and functioning trophoblast. Slit2/Robo1 signaling plays an important role in placental angiogenesis during normal pregnancy. Hence, we here investigated whether or not Slit2/Robo1 signaling also had an impact in ectopic tubal pregnancy.

Methods: The Slit2 and Robo1 expression pattern relevant to trophoblast invasive behavior and vascular remodeling was studied in human tubal placenta obtained from patients with ectopic pregnancy (5-8weeks gestation), The trophoblast development, vascular architecture and Robo1 expression pattern were observed in Slit2 overexpression (Slit2-Tg) and C57BL mice placenta (E13.5 and E15.5).

Results: Marked with CK-7 and Vimentin, the vessel profiles of fallopian tube were classified into four stages. In the presence of extravillous trophoblast (EVT), stellate-shaped and polygonal-shaped EVTs were observed, and the stellate-shaped EVT showed the higher Slit2 expression (P < 0.01) but lower Robo1 expression (P < 0.05) than polygonal-shaped cells. By contrast, a temporary Slit2 up-regulation in remodeling vessel and Slit2 down-regulation in remodeled vessel of polygonal-shape extravillous trophoblast cells occurred in tubal pregnancies. In Slit2-Tg mice E13.5 and E15.5 placenta, Slit2 overexpression promoted vascular remodeling by increasing in the diameter of the maternal blood sinusoids and fetal capillaries, but enhanced the thickness of trophoblast and vasculature at E15.5 Slit2-Tg mice.

Conclusions: The varying Slit2 and Robo1 expression in EVTs was associated with trophoblast invasion and probably plays an important role in the events of blood vessel remodeling of the fallopian tube tissues.

Keywords: Extravillous trophoblast; Slit2/Robo1; Tubal pregnancy; Vascular remodeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadherins / metabolism
  • Epithelial-Mesenchymal Transition*
  • Fallopian Tubes / pathology
  • Female
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Nerve Tissue Proteins / metabolism*
  • Pregnancy
  • Pregnancy, Tubal / metabolism*
  • Pregnancy, Tubal / pathology
  • Receptors, Immunologic / metabolism*
  • Roundabout Proteins
  • Trophoblasts / physiology*
  • Vascular Remodeling
  • Vimentin / metabolism
  • beta Catenin / metabolism

Substances

  • Cadherins
  • Intercellular Signaling Peptides and Proteins
  • Nerve Tissue Proteins
  • Receptors, Immunologic
  • Vimentin
  • beta Catenin
  • Slit homolog 2 protein