Growth factor action in neural crest cell diversification
- 1 November 1997
- journal article
- review article
- Published by Wiley in Journal of Anatomy
- Vol. 191 (4) , 493-499
- https://doi.org/10.1046/j.1469-7580.1997.19140493.x
Abstract
At the onset of their migration into the embryo, many neural crest cells are pluripotent in the sense that they have the capacity to generate progeny that consist of more than one cell type. More recently, we have found that there are pluripotent neural crest cell-derived cells even at sites of terminal differentiation. These findings support the notion that cues originating from the microenvironment, at least in part, direct neural crest cell type specification. Based on the rationale that growth factors that are known to support survival of neural crest cell derivatives may have additional functions in progenitor cell development, we have examined the action of pertinent growth factors. Trophic, mitogenic, antiproliferative and differentiation promoting activities were found. Stem cell factor (SCF) is trophic for pluripotent neural crest cells. Contrary to expectation, SCF plus a neurotrophin, rather than SCF alone is trophic for committed melanogenic cells. Basic fibroblast growth factor (bFGF) is mitogenic both for pluripotent cells and committed melanogenic cells. However, the cells become dependent on another factor for survival. Whereas any neurotrophin tested can rescue bFGF-activated pluripotent neural crest cells, the factor that rescues melanogenic cells remains to be determined. Transforming growth factor beta 1 (TGF-beta 1) is a powerful antimitotic signal for all neural crest cells that overrides the bFGF/neurotrophin proliferative signal. Furthermore, SCF promotes differentiation of neural crest cells into cells of the sensory neuron lineage. Neurotrophin-3 (NT-3) specifically promotes high affinity uptake of norepinephrine by neural crest cells and is thus thought to play a critical role in the differentiation of sympathetic neuroblasts. In summary, our data indicate that neurotrophins and other pertinent growth factors affect survival, proliferation and differentiation of neural crest cells at multiple levels and in different lineages. Moreover, our findings emphasise the importance of the concerted action of combinations of growth factors, rather than of individual factors.Keywords
This publication has 57 references indexed in Scilit:
- The Trk family of neurotrophin receptorsJournal of Neurobiology, 1994
- Steel factor is required for maintenance, but not differentiation, of melanocyte precursors in the neural crestDevelopmental Biology, 1992
- Identification of early neurogenic cells in the neural crest lineageDevelopmental Biology, 1992
- Partial restriction in the developmental potential of late emigrating avian neural crest cellsDevelopmental Biology, 1992
- In vitro clonal analysis of quail cardiac neural crest developmentDevelopmental Biology, 1991
- In vitro clonal analysis of progenitor cell patterns in dorsal root and sympathetic ganglia of the quail embryoDevelopmental Biology, 1991
- SSEA-1 is a specific marker for the spinal sensory neuron lineage in the quail embryo and in neural crest cell culturesDevelopmental Biology, 1989
- In vitro proliferation and terminal differentiation of quail neural crest cells in a defined culture mediumExperimental Cell Research, 1985
- Clonal analysis of quail neural crest cellsDevelopmental Biology, 1980
- The relationship of cell division to the acquisition of adrenergic characteristics by developing sympathetic ganglion cell precursorsDevelopmental Biology, 1978