PUBLICATION

Melanophores in the stripes of adult zebrafish do not have the nature to gather, but disperse when they have the space to move

Authors
Takahashi, G., and Kondo, S.
ID
ZDB-PUB-081218-10
Date
2008
Source
Pigment cell & melanoma research   21(6): 677-686 (Journal)
Registered Authors
Kondo, Shigeru
Keywords
melanophore, xanthophore, pigment pattern, migration, laser ablation
MeSH Terms
  • Animals
  • Body Patterning/physiology*
  • Cell Movement*
  • Chromatophores/physiology
  • Melanophores/physiology*
  • Phenotype
  • Skin Pigmentation/physiology*
  • Zebrafish/growth & development*
PubMed
19067972 Full text @ Pigment Cell Melanoma Res.
Abstract
Animal skin pattern is one of the good model systems used to study the mechanism of pattern formation. Molecular genetic studies with zebrafish have shown that pigment cells play a major role in the mechanism of stripe formation. Among the variety of cellular events that may be involved in the mechanism, aggregation of melanophores has been suggested as an important factor for pattern formation. However, only a few experimental studies detected the migration ability of melanophores in vivo. Here, we tried to determine whether melanophores really have the ability to aggregate in the skin of zebrafish. Melanophores in the adult stripes are packed densely and they rarely move. However, when the neighboring pigment cells are killed, they move and regenerate the stripe pattern, suggesting that melanophores retain the migration ability. To analyze the migration, we ablated a part of the melanophores by laser to give free space to the remaining cells; we then traced the migration. Contrary to our expectation, we found that melanophores repulsed one another and dispersed from the aggregated condition in the absence of xanthophores. Apparent aggregation may be forced by the stronger repulsive effect against the xanthophores, which excludes melanophores from the yellow stripe region.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping