Premium
Y‐27632 simplifies the isolation procedure of human primary epidermal cells by selectively blocking focal adhesion of dermal cells
Author(s) -
Wen Jie,
Zu Tingjian,
Zhou Qian,
Leng Xue,
Wu Xunwei
Publication year - 2018
Publication title -
journal of tissue engineering and regenerative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.835
H-Index - 72
eISSN - 1932-7005
pISSN - 1932-6254
DOI - 10.1002/term.2526
Subject(s) - microbiology and biotechnology , dermis , epidermis (zoology) , regeneration (biology) , stem cell , tissue engineering , progenitor cell , ex vivo , focal adhesion , in vitro , biology , chemistry , anatomy , biochemistry , signal transduction , genetics
Primary skin epidermal cells isolation and in vitro expansion culture have been widely used for laboratory research and clinical applications. The conventional methods involving sequential enzymatic digestion of adult tissues have given low cell recovery rate and reduced cell viability. We report here an advanced method for human primary epidermal progenitor cells isolation from skin tissues including the Rho kinase inhibitor Y‐27632. Compared with traditional protocols, the current protocol is simple, easy, and faster; moreover, it gives a greater yield of integrin‐expressing epithelial stem cells. In addition, our new methodology does not require a separation of epidermis from dermis because the medium selectively blocks focal adhesion and growth of dermal cells. Importantly, the cells isolated from this method can maintain their regeneration potential and quickly reconstitute a mature human skin in vivo after grafting onto nude mice. In brief, we describe here a simple (one step) and serum‐free method for isolating primary epidermal stem cells from adult tissues. The isolated cells may be widely used for both laboratory studies and clinical application, especially in the field of tissue engineering and regeneration.