ZFIN ID: ZDB-PUB-130211-11
On the embryonic origin of adult melanophores: the role of ErbB and Kit signalling in establishing melanophore stem cells in zebrafish
Dooley, C.M., Mongera, A., Walderich, B., and Nüsslein-Volhard, C.
Date: 2013
Source: Development (Cambridge, England) 140(5): 1003-1013 (Journal)
Registered Authors: Dooley, Christopher, Nüsslein-Volhard, Christiane, Walderich, Brigitte
Keywords: none
MeSH Terms: Age Factors; Animals; Animals, Genetically Modified; Cell Lineage/genetics*; Cell Movement/genetics (all 27) expand
PubMed: 23364329 Full text @ Development
FIGURES   (current status)
ABSTRACT

Pigment cells in vertebrates are derived from the neural crest (NC), a pluripotent and migratory embryonic cell population. In fishes, larval melanophores develop during embryogenesis directly from NC cells migrating along dorsolateral and ventromedial paths. The embryonic origin of the melanophores that emerge during juvenile development in the skin to contribute to the striking colour patterns of adult fishes remains elusive. We have identified a small set of melanophore progenitor cells (MPs) in the zebrafish (Danio rerio, Cyprinidae) that is established within the first 2 days of embryonic development in close association with the segmentally reiterated dorsal root ganglia (DRGs). Lineage analysis and 4D in vivo imaging indicate that progeny of these embryonic MPs spread segmentally, giving rise to the melanophores that create the adult melanophore stripes. Upon depletion of larval melanophores by morpholino knockdown of Mitfa, the embryonic MPs are prematurely activated; their progeny migrate along the spinal nerves restoring the larval pattern and giving rise to postembryonic MPs associated with the spinal nerves. Mutational or chemical inhibition of ErbB receptors blocks all early NC migration along the ventromedial path, causing a loss of DRGs and embryonic MPs. We show that the sparse like (slk) mutant lacks larval and metamorphic melanophores and identify kit ligand a (kitlga) as the underlying gene. Our data suggest that kitlga is required for the establishment or survival of embryonic MPs. We propose a model in which DRGs provide a niche for the stem cells of adult melanophores.

ADDITIONAL INFORMATION