Defects in pathfinding by cranial neural crest cells in mice lacking the neuregulin receptor ErbB4.

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 Biol

journal_title

Nature cell biology

authors

Golding JP,Trainor P,Krumlauf R,Gassmann M

doi

10.1038/35000058

keywords:

subject

Has Abstract

pub_date

2000-02-01 00:00:00

pages

103-9

issue

2

eissn

1465-7392

issn

1476-4679

journal_volume

2

pub_type

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