Syndecan-1 regulates BMP signaling and dorso-ventral patterning of the ectoderm during early Xenopus development

Dev Biol. 2009 May 15;329(2):338-49. doi: 10.1016/j.ydbio.2009.03.007. Epub 2009 Mar 18.

Abstract

Extracellular regulation of growth factor signaling is a key event for embryonic patterning. Heparan sulfate proteoglycans (HSPG) are among the molecules that regulate this signaling during embryonic development. Here we study the function of syndecan1 (Syn1), a cell-surface HSPG expressed in the non-neural ectoderm during early development of Xenopus embryos. Overexpression of Xenopus Syn1 (xSyn1) mRNA is sufficient to reduce BMP signaling, induce chordin expression and rescue dorso-ventral patterning in ventralized embryos. Experiments using chordin morpholinos established that xSyn1 mRNA can inhibit BMP signaling in the absence of chordin. Knockdown of xSyn1 resulted in a reduction of BMP signaling and expansion of the neural plate with the concomitant reduction of the non-neural ectoderm. Overexpression of xSyn1 mRNA in xSyn1 morphant embryos resulted in a biphasic effect, with BMP being inhibited at high concentrations and activated at low concentrations of xSyn1. Interestingly, the function of xSyn1 on dorso-ventral patterning and BMP signaling is specific for this HSPG. In summary, we report that xSyn1 regulates dorso-ventral patterning of the ectoderm through modulation of BMP signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Body Patterning / physiology*
  • Bone Morphogenetic Proteins / metabolism*
  • DNA Primers
  • Ectoderm / embryology*
  • RNA, Messenger / genetics
  • RNA, Small Interfering
  • Signal Transduction / physiology*
  • Syndecan-1 / genetics
  • Syndecan-1 / physiology*
  • Xenopus laevis / embryology*

Substances

  • Bone Morphogenetic Proteins
  • DNA Primers
  • RNA, Messenger
  • RNA, Small Interfering
  • Syndecan-1