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Development. 2014 Jan;141(2):318-24. doi: 10.1242/dev.099804. Epub 2013 Dec 4.

Involvement of Delta/Notch signaling in zebrafish adult pigment stripe patterning.

Author information

1
Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.

Erratum in

  • Development. 2014 Mar;141(6):1418.

Abstract

The skin pigment pattern of zebrafish is a good model system in which to study the mechanism of biological pattern formation. Although it is known that interactions between melanophores and xanthophores play a key role in the formation of adult pigment stripes, molecular mechanisms for these interactions remain largely unknown. Here, we show that Delta/Notch signaling contributes to these interactions. Ablation of xanthophores in yellow stripes induced the death of melanophores in black stripes, suggesting that melanophores require a survival signal from distant xanthophores. We found that deltaC and notch1a were expressed by xanthophores and melanophores, respectively. Moreover, inhibition of Delta/Notch signaling killed melanophores, whereas activation of Delta/Notch signaling ectopically in melanophores rescued the survival of these cells, both in the context of pharmacological inhibition of Delta/Notch signaling and after ablation of xanthophores. Finally, we showed by in vivo imaging of cell membranes that melanophores extend long projections towards xanthophores in the yellow stripes. These data suggest that Delta/Notch signaling is responsible for a survival signal provided by xanthophores to melanophores. As cellular projections can enable long-range interaction between membrane-bound ligands and their receptors, we propose that such projections, combined with direct cell-cell contacts, can substitute for the effect of a diffusible factor that would be expected by the conventional reaction-diffusion (Turing) model.

KEYWORDS:

Delta/Notch signal; Pigment pattern; Turing mechanism

Comment in

PMID:
24306107
PMCID:
PMC3879813
DOI:
10.1242/dev.099804
[Indexed for MEDLINE]
Free PMC Article

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