小眼畸形相关转录因子
黑素细胞
白癜风
诱导多能干细胞
生物
毛囊
移植
脱色
细胞生物学
乘客3
黑色素
干细胞
表皮(动物学)
癌症研究
色素减退
黑素皮质素1受体
黑色素瘤
免疫学
解剖
医学
内科学
表型
遗传学
胚胎干细胞
基因
转录因子
作者
Li‐Ping Liu,Yumei Li,Ningning Guo,Shu Li,Xiaolong Ma,Yixuan Zhang,Yimeng Gao,Jianling Huang,Dongxu Zheng,Lu-Yuan Wang,Hui Xu,Lijian Hui,Yun‐Wen Zheng
出处
期刊:Cell Reports
[Cell Press]
日期:2019-04-01
卷期号:27 (2): 455-466.e5
被引量:44
标识
DOI:10.1016/j.celrep.2019.03.046
摘要
Induced pluripotent stem cells (iPSCs) are a promising melanocyte source as they propagate indefinitely and can be established from patients. However, the in vivo functions of human iPSC-derived melanocytes (hiMels) remain unknown. Here, we generated hiMels from vitiligo patients using a three-dimensional system with enhanced differentiation efficiency, which showed characteristics of human epidermal melanocytes with high sequence similarity and involved in multiple vitiligo-associated signaling pathways. A modified hair follicle reconstitution assay in vivo showed that MITF+PAX3+TYRP1+ hiMels were localized in the mouse hair bulb and epidermis and produced melanin up to 7 weeks after transplantation, whereas MITF+PAX3+TYRP1− hiMelanocyte stem cells integrated into the bulge-subbulge regions. Overall, these data demonstrate the long-term functions of hiMels in vivo to reconstitute pigmented hair follicles and to integrate into normal regions for both mature melanocytes and melanocyte stem cells, providing an alternative source of personalized cellular therapy for depigmentation.
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