Galectin-4 expression is down-regulated in response to autophagy during differentiation of rat trophoblast cells

Sci Rep. 2016 Aug 30:6:32248. doi: 10.1038/srep32248.

Abstract

Placental development and trophoblast invasion of the maternal endometrium establish the maternal-fetal interface, which is critical for the developing embryo and fetus. Herein we show that overexpression of Galectin-4 (Gal-4) during trophoblast differentiation inhibited the enlargement of Rcho-1 cells (a model for rat trophoblast differentiation) and promoted cell-cell adhesion, whereas trophoblast specific markers and MMP-9 activity were not affected. In the rat placenta, microtubule associated protein 1 light chain 3 alpha (LC3) protein, an autophagy marker, is highly expressed on the maternal side of the decidua where Gal-4 expression is weak. In vitro assays showed that the expression of trophoblast-specific differentiation markers was reduced by 3-Methyladenine (3-MA) and Bafilomycin A1, known as autophagy inhibitors, compared to control cells. Furthermore, Gal-4 expression in Rcho-1 cells, which is normally down-regulated during differentiation, was not attenuated in the presence of autophagy inhibitors, suggesting that autophagy is upstream of Gal-4 expression. We herein describe a possible mechanism by which autophagy regulates trophoblast differentiation via regulation of Gal-4 expression in order to establish the maternal-fetal interface.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / genetics*
  • Cell Adhesion / genetics
  • Cell Differentiation / genetics*
  • Cell Line, Tumor
  • Down-Regulation*
  • Female
  • Galectin 4 / genetics*
  • Galectin 4 / metabolism
  • Gene Expression Regulation, Developmental*
  • Placenta / metabolism
  • Placentation / genetics
  • Pregnancy
  • Rats, Wistar
  • Time-Lapse Imaging / methods
  • Trophoblasts / metabolism*

Substances

  • Galectin 4