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 language | American English |
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Journal | The Journal of Cell Biology |
Volume | 175 |
State | Published - 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