RNA-Seq identifies genes whose proteins are upregulated during syncytia development in murine C2C12 myoblasts and human BeWo trophoblasts

Physiol Rep. 2021 Jan;9(1):e14671. doi: 10.14814/phy2.14671.

Abstract

The fusion of villous cytotrophoblasts into the multinucleated syncytiotrophoblast is critical for the essential functions of the mammalian placenta. Using RNA-Seq gene expression, quantitative protein expression, and siRNA knockdown we identified genes and their cognate proteins which are similarly upregulated in two cellular models of mammalian syncytia development (human BeWo cytotrophoblast to syncytiotrophoblast and murine C2C12 myoblast to myotube). These include DYSF, PDE4DIP, SPIRE2, NDRG1, PLEC, GPR146, HSPB8, DHCR7, and HDAC5. These findings provide avenues for further understanding of the mechanisms underlying mammalian placental syncytiotrophoblast development.

Keywords: cell fusion; placenta; syncytialization.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Fusion / methods*
  • Cells, Cultured
  • Female
  • Giant Cells / cytology
  • Giant Cells / metabolism*
  • Humans
  • Mice
  • Myoblasts / cytology
  • Myoblasts / metabolism*
  • Placenta / cytology
  • Placenta / metabolism*
  • Pregnancy
  • RNA-Seq / methods*
  • Trophoblasts / cytology
  • Trophoblasts / metabolism*