MyoD-Positive Epiblast Cells Regulate Skeletal Muscle Differentiation in the Embryo

Jacquelyn Gerhart, Justin Elder, Christine Neely, Jared Schure, Tage Kvist, Karen Knudsen, Mindy George-Weinstein

Research output: Contribution to journalArticlepeer-review

Abstract

MyoD mRNA is expressed in a subpopulation of cells within the embryonic epiblast. Most of these cells are incorporated into somites and synthesize Noggin. Ablation of MyoD-positive cells in the epiblast subsequently results in the herniation of organs through the ventral body wall, a decrease in the expression of Noggin, MyoD, Myf5, and myosin in the somites and limbs, and an increase in Pax-3-positive myogenic precursors. The addition of Noggin lateral to the somites compensates for the loss of MyoD-positive epiblast cells. Skeletal muscle stem cells that arise in the epiblast are utilized in the somites to promote muscle differentiation by serving as a source of Noggin.

Original languageAmerican English
JournalThe Journal of Cell Biology
Volume175
StatePublished - Oct 23 2006

Keywords

  • Animals
  • Carrier Proteins
  • Cell Differentiation
  • Chick Embryo
  • Developmental
  • Embryo
  • Epithelium
  • Extremities
  • Fluorescent Antibody Technique
  • Gene Expression Regulation
  • In Situ Hybridization
  • Mammalian
  • Morphogenesis
  • Muscle
  • MyoD Protein
  • Myogenic Regulatory Factor 5
  • Myosins
  • Nonmammalian
  • Paired Box Transcription Factors
  • Skeletal
  • Somites
  • Stem Cells

Disciplines

  • Cell Biology
  • Developmental Biology
  • Medicine and Health Sciences

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