Abstract:
:Mouse embryos with a loss-of-function mutation in the gene encoding the receptor tyrosine kinase ErbB4 exhibit misprojections of cranial sensory ganglion afferent axons. Here we analyse ErbB4-deficient mice, and find that morphological differences between wild-type and mutant cranial ganglia correlate with aberrant migration of a subpopulation of hindbrain-derived cranial neural crest cells within the paraxial mesenchyme environment. In transplantation experiments using new grafting techniques in cultured mouse embryos, we determine that this phenotype is non-cell-autonomous: wild-type and mutant neural crest cells both migrate in a pattern consistent with the host environment, deviating from their normal pathway only when transplanted into mutant embryos. ErbB4 signalling events within the hindbrain therefore provide patterning information to cranial paraxial mesenchyme that is essential for the proper migration of neural crest cells.
journal_name
Nat Cell Bioljournal_title
Nature cell biologyauthors
Golding JP,Trainor P,Krumlauf R,Gassmann Mdoi
10.1038/35000058keywords:
subject
Has Abstractpub_date
2000-02-01 00:00:00pages
103-9issue
2eissn
1465-7392issn
1476-4679journal_volume
2pub_type
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