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Dissection, Culture and Analysis of Primary Cranial Neural Crest Cells from Mouse for the Study of Neural Crest Cell Delamination and Migration
Published on: October 3, 2019
Abnormalities in neural crest cell migration in laminin alpha5 mutant mice
Edward G Coles1, Laura S Gammill, Jeffrey H Miner
1Division of Biology, California Institute of Technology, Pasadena, 91125, USA.
Developmental Biology
|December 1, 2005
Summary
Laminin alpha5 restricts neural crest cell migration and aids in ganglion formation. This protein is crucial for the proper migration and differentiation of specific neural crest populations during embryonic development.
Area of Science:
- Developmental Biology
- Cell Biology
- Molecular Biology
Background:
- Extracellular matrix molecules like laminin are suggested to influence neural crest migration in vitro.
- The in vivo function of laminin in embryonic development, particularly in neural crest cell behavior, remains largely unknown.
Purpose of the Study:
- To investigate the role of laminin alpha5 in neural crest cell migration and ganglion formation during embryonic development.
- To elucidate the function of laminin alpha5 as a potential regulator of neural crest cell pathways and differentiation.
Main Methods:
- Localization studies of laminin alpha5 in chick and mouse embryos.
- Analysis of neural crest migration in laminin alpha5 mutant mice.
- In vitro experiments exposing neural folds to laminin alpha5.
Main Results:
- Laminin alpha5 is localized in neural folds and neural crest migratory pathways in chick and mouse embryos.
- Laminin alpha5 mutant mice exhibit expanded neural crest migratory streams.
- In vitro, laminin alpha5 reduces the number of migratory neural crest cells.
- Mutants show defects in cranial sensory and trunk sympathetic ganglia condensation, with apparent recovery later.
Conclusions:
- Laminin alpha5 acts as a restrictive cue for neural crest cells, focusing their migration and condensation into ganglia.
- Laminin alpha5 is essential for the proper migration and timely differentiation of specific neural crest cell populations.
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