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A distinct developmental programme for the cranial paraxial mesoderm in the chick embryo
1Department of Developmental Neurobiology, UMDS, Guy's Hospital, London, SE1 9RT, UK.
Summary
Cranial paraxial mesoderm cells migrate to branchial arches to form head muscles. Trunk somitic mesoderm can also migrate cranially, but gene expression changes upon arrival, indicating environmental influence on muscle development.
Area of Science:
- Developmental Biology
- Cell Migration
- Molecular Biology
Background:
- Cranial paraxial mesoderm contributes to head skull and muscle formation.
- Mesoderm cells migrate from the hindbrain region to branchial arches for muscle differentiation.
Purpose of the Study:
- To characterize migratory pathways of cranial paraxial mesoderm cells.
- To investigate gene expression changes in migrating and differentiating myogenic cells.
- To determine the potential of trunk mesoderm to contribute to cranial muscle development.
Main Methods:
- DiI-labeling of chick embryo mesoderm cells.
- Orthotopic grafting of quail cranial paraxial mesoderm.
- Grafting of quail trunk mesoderm into cranial regions.
- Analysis of myogenic gene expression (Myf5, MyoD, myogenin, Pax3, Pax1).
Main Results:
- Cranial paraxial mesoderm cells migrate to specific branchial arches based on their position.
- Myogenic gene expression in branchial arch muscles occurs later than in somites.
- Pax3 is not expressed in migrating branchial arch myogenic cells.
- Somitic mesoderm, but not segmental plate mesoderm, can migrate cranially and integrate into branchial arch muscles.
- Migrating somitic cells downregulate Pax3 in the branchial arches, suggesting environmental regulation.
Conclusions:
- Hindbrain and branchial arch signals influence gene expression and developmental trajectories of migrating myogenic cells.
- Environmental cues play a critical role in modulating gene expression and differentiation pathways of mesoderm-derived muscle cells.