Tfap2b specifies an embryonic melanocyte stem cell that retains adult multifate potential

被引:21
作者
Brombin, Alessandro [1 ,2 ]
Simpson, Daniel J. [1 ]
Travnickova, Jana [1 ,2 ]
Brunsdon, Hannah [1 ,2 ]
Zeng, Zhiqiang [1 ,2 ]
Lu, Yuting [1 ,2 ]
Young, Adelaide I. J. [1 ,2 ]
Chandra, Tamir [1 ]
Patton, E. Elizabeth [1 ,2 ]
机构
[1] Univ Edinburgh, Inst Genet & Canc, MRC Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, CRUK Edinburgh Ctr, Inst Genet & Canc, Edinburgh EH4 2XU, Midlothian, Scotland
基金
欧洲研究理事会; 英国医学研究理事会; 欧盟地平线“2020”;
关键词
NEURAL CREST DEVELOPMENT; RNA-SEQ DATA; RIBOSOME BIOGENESIS; HUMAN PIGMENTATION; ZEBRAFISH; ORIGIN; EXPRESSION; KIT; PROGENITORS; MULTIPOTENT;
D O I
10.1016/j.celrep.2021.110234
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Melanocytes, the pigment-producing cells, are replenished from multiple stem cell niches in adult tissue. Although pigmentation traits are known risk factors for melanoma, we know little about melanocyte stem cell (McSC) populations other than hair follicle McSCs and lack key lineage markers with which to identify McSCs and study their function. Here we find that Tfap2b and a select set of target genes specify an McSC population at the dorsal root ganglia in zebrafish. Functionally, Tfap2b is required for only a few late-stage embryonic melanocytes, and is essential for McSC-dependent melanocyte regeneration. Fate mapping data reveal that tfap2b(+) McSCs have multifate potential, and are the cells of origin for large patches of adult melanocytes, two other pigment cell types (iridophores and xanthophores), and nerve-associated cells. Hence, Tfap2b confers McSC identity in early development, distinguishing McSCs from other neural crest and pigment cell lineages, and retains multifate potential in the adult zebrafish.
引用
收藏
页数:23
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