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ORAI1 calcium channel orchestrates skin homeostasis.


ABSTRACT: To achieve and maintain skin architecture and homeostasis, keratinocytes must intricately balance growth, differentiation, and polarized motility known to be governed by calcium. Orai1 is a pore subunit of a store-operated Ca(2+) channel that is a major molecular counterpart for Ca(2+) influx in nonexcitable cells. To elucidate the physiological significance of Orai1 in skin, we studied its functions in epidermis of mice, with targeted disruption of the orai1 gene, human skin sections, and primary keratinocytes. We demonstrate that Orai1 protein is mainly confined to the basal layer of epidermis where it plays a critical role to control keratinocyte proliferation and polarized motility. Orai1 loss of function alters keratinocyte differentiation both in vitro and in vivo. Exploring underlying mechanisms, we show that the activation of Orai1-mediated calcium entry leads to enhancing focal adhesion turnover via a PKC?-Calpain-focal adhesion kinase pathway. Our findings provide insight into the functions of the Orai1 channel in the maintenance of skin homeostasis.

SUBMITTER: Vandenberghe M 

PROVIDER: S-EPMC3864283 | biostudies-other | 2013 Dec

REPOSITORIES: biostudies-other

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ORAI1 calcium channel orchestrates skin homeostasis.

Vandenberghe Matthieu M   Raphaël Maylis M   Lehen'kyi V'yacheslav V   Gordienko Dmitri D   Hastie Ryan R   Oddos Thierry T   Rao Anjana A   Hogan Patrick G PG   Skryma Roman R   Prevarskaya Natalia N  

Proceedings of the National Academy of Sciences of the United States of America 20131125 50


To achieve and maintain skin architecture and homeostasis, keratinocytes must intricately balance growth, differentiation, and polarized motility known to be governed by calcium. Orai1 is a pore subunit of a store-operated Ca(2+) channel that is a major molecular counterpart for Ca(2+) influx in nonexcitable cells. To elucidate the physiological significance of Orai1 in skin, we studied its functions in epidermis of mice, with targeted disruption of the orai1 gene, human skin sections, and prima  ...[more]

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