Thomas Aaron J, Erickson Carol A
Department of Molecular and Cellular Biology, University of California at Davis, Davis, CA, USA.
Pigment Cell Melanoma Res. 2008 Dec;21(6):598-610. doi: 10.1111/j.1755-148X.2008.00506.x.
Melanocytes differentiate from the neural crest (NC), which is a transient population of cells that delaminates from the neural tube and migrates extensively throughout the embryo during vertebrate development. Melanoblast specification from NC precursors is a progressive process during which initially pluripotent cells become restricted to the melanogenic lineage and adopt the gene expression profile and morphology of melanocytes. This specification process is governed primarily by Wnt and BMP signaling molecules, although other signaling pathways, such as those activated by Kit and Endothelin 3, can also stimulate melanogenesis. The transcriptional repressor FoxD3 occupies a central role in melanocyte fate determination by repressing melanogenesis in premigratory NC cells and in other NC lineages.
黑素细胞由神经嵴(NC)分化而来,神经嵴是一群短暂存在的细胞,在脊椎动物发育过程中从神经管分层并广泛迁移至整个胚胎。从神经嵴前体细胞形成黑素母细胞是一个渐进过程,在此过程中,最初具有多能性的细胞逐渐局限于黑素生成谱系,并呈现黑素细胞的基因表达谱和形态。尽管其他信号通路,如由Kit和内皮素3激活的信号通路,也能刺激黑素生成,但这一特化过程主要由Wnt和BMP信号分子调控。转录抑制因子FoxD3通过抑制迁移前神经嵴细胞和其他神经嵴谱系中的黑素生成,在黑素细胞命运决定中发挥核心作用。