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Electric fields guide migration of epidermal stem cells and promote skin wound healing
Author(s) -
Li Li,
Gu Wei,
Du Juan,
Reid Brian,
Deng Xianjian,
Liu Zhidai,
Zong Zhaowen,
Wang Haiyan,
Yao Bo,
Yang Ce,
Yan Jun,
Zeng Ling,
Chalmers Laura,
Zhao Min,
Jiang Jianxin
Publication year - 2012
Publication title -
wound repair and regeneration
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.847
H-Index - 109
eISSN - 1524-475X
pISSN - 1067-1927
DOI - 10.1111/j.1524-475x.2012.00829.x
Subject(s) - wound healing , microbiology and biotechnology , pi3k/akt/mtor pathway , cell migration , epidermal growth factor , epidermis (zoology) , extracellular , signal transduction , protein kinase a , kinase , biology , chemistry , cancer research , receptor , immunology , cell , anatomy , biochemistry
Migration of epidermal stem cells ( EpSCs ) into wounds may play an important role in wound healing. Endogenous electric fields ( EFs ) arise naturally at wounds. Consistent with previous reports, we measured outward electric currents at rat skin wounds using vibrating probes. Topical use of prostaglandin E2 significantly promoted wound healing. However, it is not known whether EpSCs respond to EFs . We first isolated and characterized EpSCs from rat skin. We then demonstrated that EpSCs isolated from the epidermis migrated directionally toward the cathode in EFs of 50–400 mV /mm. The directedness values increased in a dose‐ and time‐dependent fashion. The migration speed of EpSCs was significantly increased in EFs . EFs induced asymmetric polymerization of intracellular F ‐actin and activation of the extracellular signal‐regulated kinase 1/2 and phosphatidylinositol‐3‐kinase ( PI3K )/protein kinase B pathways. Inhibition of epidermal growth factor receptor, extracellular signal‐regulated kinase 1/2, or PI3K significantly inhibited the cathodal distribution of F ‐actin and the electrotactic response of EpSCs . These data for the first time show that EpSCs possess obvious electrotaxis, in which the epidermal growth factor receptor–mitogen activated protein kinase– PI3K pathways are involved. These data thus suggest a novel aspect of electric signaling in wound healing—to stimulate and guide migration of EpSCs and to regulate wound healing.