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Endothelin 3 promotes neural crest cell proliferation and mediates a vast increase in melanocyte number in culture.

机译:内皮素3促进神经c细胞增殖并介导培养物中黑素细胞数量的大量增加。

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摘要

Mutations in the endothelin 3 (EDN3) gene severely affect the development of neural crest-derived melanocytes. In this paper, we report the action of EDN3 on neural crest cells in vitro. The presence of EDN3 leads to a large increase in the number of cells, the majority of which eventually differentiate into melanocytes that aggregate to form a reproducible pigmentation pattern. Quantitative analysis of the effect of different culture conditions revealed that EDN3 initially promotes neural crest cell proliferation. This phase of expansion, which can be prolonged for a few weeks if the cells are replaced regularly, is followed by both a decrease in cell proliferation and the onset of melanocytic differentiation. Therefore, EDN3 is a potent mitogen for early neural crest cell precursors that can give rise to melanocytes.
机译:内皮素3(EDN3)基因的突变会严重影响神经c衍生黑素细胞的发育。在本文中,我们报道了EDN3在体外对神经c细胞的作用。 EDN3的存在导致细胞数量大量增加,其中大多数最终分化为黑色素细胞,这些黑色素细胞聚集形成可再现的色素沉着模式。定量分析不同培养条件的影响表明,EDN3最初促进神经c细胞增殖。这个扩张阶段,如果定期更换细胞,可以延长数周,随后是细胞增殖减少和黑素细胞分化的开始。因此,EDN3是早期神经c细胞前体的有效促分裂原,它可产生黑色素细胞。

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