Callahan Scott J, Mica Yvonne, Studer Lorenz
The Center for Stem Cell Biology, Developmental Biology Program, Memorial Sloan-Kettering Cancer Center; Cancer Biology and Genetics Program, Gerstner Sloan-Kettering Graduate School, Sloan-Kettering Institute for Cancer Research.
Thermo Fisher Scientific.
J Vis Exp. 2016 Mar 3(109):e53806. doi: 10.3791/53806.
Human pluripotent stem cells (hPSCs) represent a platform to study human development in vitro under both normal and disease conditions. Researchers can direct the differentiation of hPSCs into the cell type of interest by manipulating the culture conditions to recapitulate signals seen during development. One such cell type is the melanocyte, a pigment-producing cell of neural crest (NC) origin responsible for protecting the skin against UV irradiation. This protocol presents an extension of a currently available in vitro Neural Crest differentiation protocol from hPSCs to further differentiate NC into fully pigmented melanocytes. Melanocyte precursors can be enriched from the Neural Crest protocol via a timed exposure to activators of WNT, BMP, and EDN3 signaling under dual-SMAD-inhibition conditions. The resultant melanocyte precursors are then purified and matured into fully pigmented melanocytes by culture in a selective medium. The resultant melanocytes are fully pigmented and stain appropriately for proteins characteristic of mature melanocytes.
人多能干细胞(hPSCs)是一个在正常和疾病条件下体外研究人类发育的平台。研究人员可以通过操纵培养条件来重现发育过程中出现的信号,从而将hPSCs定向分化为感兴趣的细胞类型。其中一种细胞类型是黑素细胞,它是一种起源于神经嵴(NC)的色素生成细胞,负责保护皮肤免受紫外线照射。本方案是目前可用的从hPSCs体外神经嵴分化方案的扩展,以进一步将神经嵴细胞分化为完全色素化的黑素细胞。在双SMAD抑制条件下,通过定时暴露于WNT、BMP和EDN3信号通路的激活剂,可以从神经嵴方案中富集黑素细胞前体。然后将所得的黑素细胞前体纯化,并通过在选择性培养基中培养使其成熟为完全色素化的黑素细胞。所得的黑素细胞完全色素化,并对成熟黑素细胞特有的蛋白质进行适当染色。