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Related Experiment Video

Updated: Jun 6, 2026

A Quantitative Cell Migration Assay for Murine Enteric Neural Progenitors
08:26

A Quantitative Cell Migration Assay for Murine Enteric Neural Progenitors

Published on: September 18, 2013

Bone morphogenetic proteins regulate enteric gliogenesis by modulating ErbB3 signaling.

Alcmène Chalazonitis1, Fabien D'Autréaux, Tuan D Pham

  • 1Department of Pathology & Cell Biology, Columbia University, New York, NY 10032, USA. ac83@columbia.edu

Developmental Biology
|November 25, 2010
PubMed
Summary
This summary is machine-generated.

Bone morphogenetic proteins (BMPs) are crucial for enteric gliogenesis, promoting glial cell development in the gut's nervous system by enhancing responsiveness to ErbB3 ligands.

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Last Updated: Jun 6, 2026

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Analyzing Murine Schwann Cell Development Along Growing Axons
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Published on: November 21, 2012

Area of Science:

  • Developmental Biology
  • Neuroscience
  • Gastroenterology

Background:

  • The enteric nervous system (ENS) is derived from neural crest-derived cells (ENCDC).
  • Bone morphogenetic proteins (BMPs) are known to influence neuronal differentiation in the ENS.
  • The role of BMPs in enteric gliogenesis (glial cell development) remains largely unexplored.

Purpose of the Study:

  • To investigate the role of BMPs (specifically BMPs 2 and 4) in enteric gliogenesis.
  • To determine if BMPs promote glial differentiation similarly to their known role in neuronal differentiation.
  • To elucidate the molecular mechanisms by which BMPs influence glial cell development in the ENS.

Main Methods:

  • Analysis of enteric gliogenesis in mice with altered BMP signaling (noggin overexpression or BMP4 overexpression).
  • In vitro studies using immunoisolated ENCDC treated with BMPs.
  • Assessment of phosphorylated SMAD proteins, glial differentiation markers, ErbB3 expression, and glial apoptosis.

Main Results:

  • BMP signaling modulation significantly altered glial density and the glia/neuron ratio in the ENS.
  • BMPs enhanced glial differentiation and ErbB3 receptor expression in ENCDC.
  • The ErbB3 ligand, glial growth factor 2 (GGF2), stimulated gliogenesis and proliferation, while BMPs increased dependence on GGF2.

Conclusions:

  • BMPs are essential for enteric gliogenesis, playing a key role in glial cell development within the ENS.
  • BMPs likely function by increasing the responsiveness of ENCDC to ErbB3 ligands like GGF2.
  • These findings reveal a novel mechanism regulating glial cell fate and proliferation in the developing enteric nervous system.