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用于疾病建模和再生医学应用的黑素细胞干细胞研究

Understanding Melanocyte Stem Cells for Disease Modeling and Regenerative Medicine Applications.

作者信息

Mull Amber N, Zolekar Ashwini, Wang Yu-Chieh

机构信息

Department of Pharmaceutical Sciences, University of North Texas Health Science Center, 3500 Camp Bowie Boulevard, Fort Worth, TX 76107, USA.

出版信息

Int J Mol Sci. 2015 Dec 21;16(12):30458-69. doi: 10.3390/ijms161226207.

Abstract

Melanocytes in the skin play an indispensable role in the pigmentation of skin and its appendages. It is well known that the embryonic origin of melanocytes is neural crest cells. In adult skin, functional melanocytes are continuously repopulated by the differentiation of melanocyte stem cells (McSCs) residing in the epidermis of the skin. Many preceding studies have led to significant discoveries regarding the cellular and molecular characteristics of this unique stem cell population. The alteration of McSCs has been also implicated in several skin abnormalities and disease conditions. To date, our knowledge of McSCs largely comes from studying the stem cell niche of mouse hair follicles. Suggested by several anatomical differences between mouse and human skin, there could be distinct features associated with mouse and human McSCs as well as their niches in the skin. Recent advances in human pluripotent stem cell (hPSC) research have provided us with useful tools to potentially acquire a substantial amount of human McSCs and functional melanocytes for research and regenerative medicine applications. This review highlights recent studies and progress involved in understanding the development of cutaneous melanocytes and the regulation of McSCs.

摘要

皮肤中的黑素细胞在皮肤及其附属器的色素沉着过程中发挥着不可或缺的作用。众所周知,黑素细胞的胚胎起源是神经嵴细胞。在成年皮肤中,功能性黑素细胞通过位于皮肤表皮的黑素细胞干细胞(McSCs)的分化而不断得到补充。许多先前的研究已经在这种独特干细胞群体的细胞和分子特征方面取得了重大发现。McSCs的改变也与多种皮肤异常和疾病状况有关。迄今为止,我们对McSCs的了解很大程度上来自于对小鼠毛囊干细胞微环境的研究。鉴于小鼠和人类皮肤之间存在一些解剖学差异,小鼠和人类的McSCs及其在皮肤中的微环境可能存在不同的特征。人类多能干细胞(hPSC)研究的最新进展为我们提供了有用的工具,有可能获得大量的人类McSCs和功能性黑素细胞,用于研究和再生医学应用。本综述重点介绍了在理解皮肤黑素细胞发育和McSCs调控方面的最新研究和进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c590/4691150/5e04bfe30d01/ijms-16-26207-g001.jpg

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