PMID:11401406

Citation	Wehrle-Haller, B, Meller, M and Weston, JA (2001) Analysis of melanocyte precursors in Nf1 mutants reveals that MGF/KIT signaling promotes directed cell migration independent of its function in cell survival. Dev. Biol. 232:471-83
Abstract	Neural crest-derived melanocyte precursors (MPs) in avian and murine embryos emerge from the dorsal neural tube into a migration staging area (MSA). MPs subsequently migrate from the MSA on a dorsolateral pathway between the dermamyotome and the overlying epithelium. In mouse embryos, MPs express the receptor tyrosine kinase, KIT, and require its cognate ligand, Mast cell growth factor (MGF), for survival and differentiation. Prior to the onset of MP migration, MGF is expressed on the dorsolateral pathway at some distance from cells in the MSA and appears to be required for normal MP development. To learn if MGF is required solely for MP survival on this pathway, or if it also provides directional cues for migration, we uncoupled survival from chemoattractive or motogenic functions of this ligand using mice that carry a targeted mutation at the Neurofibromin (Nf1) locus and consequently lack RAS-GAP function. We show that Nf1-mutant MPs survive in the absence of MGF in vitro and in vivo and that Nf1-mutant MPs disperse normally on the lateral migration pathway in the presence of MGF. In contrast, Nf1-mutant MPs persist in the location of the MSA but are not observed on the lateral migration pathway in double-mutant mice that also lack MGF. We conclude that MGF/KIT function provides a signal required for directed migration of the MPs on the lateral pathway in vivo, independent of its function in survival. We further suggest that the MGF mediates MP migration through a signaling pathway that does not involve RAS.
Links	PubMed Online version:10.1006/dbio.2001.0167
Keywords	Animals; Cell Differentiation; Cell Movement/physiology; Cell Survival; Melanocytes/cytology; Melanocytes/physiology; Mice; Mice, Inbred C57BL; Mice, Knockout; Models, Biological; Mutation; Nerve Tissue Proteins/genetics; Nerve Tissue Proteins/physiology; Neural Crest/cytology; Neurofibromin 1; Oncogene Proteins/physiology; Proto-Oncogene Proteins c-kit; Signal Transduction; Stem Cell Factor/genetics; Stem Cell Factor/physiology; Stem Cells/cytology; Stem Cells/physiology; ras GTPase-Activating Proteins/physiology
edit table

Annotations

Gene product	Qualifier	GO ID	GO term name	Evidence Code	with/from	Aspect	Notes	Status
edit table

References

See Help:References for how to manage references in GONUTS.