2017年6月
Phospholipase Cδ 1 regulates p38 MAPK activity and skin barrier integrity
Cell Death and Differentiation
- 巻
- 24
- 号
- 6
- 開始ページ
- 1079
- 終了ページ
- 1090
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1038/cdd.2017.56
© 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. Keratinocytes undergo a unique type of programmed cell death known as cornification, which leads to the formation of the stratum corneum (SC), the main physical barrier of the epidermis. A defective epidermal barrier is a hallmark of the two most common inflammatory skin disorders, psoriasis, and atopic dermatitis. However, the detailed molecular mechanisms of skin barrier formation are not yet fully understood. Here, we showed that downregulation of phospholipase C (PLC) d 1, a Ca 2+-mobilizing and phosphoinositide-metabolizing enzyme abundantly expressed in the epidermis, impairs the barrier functions of the SC. PLCd 1 downregulation also impairs localization of tight junction proteins. Loss of PLCd 1 leads to a decrease in intracellular Ca 2+ concentrations and nuclear factor of activated T cells activity, along with hyperactivation of p38 mitogen-activated protein kinase (MAPK) and inactivation of RhoA. Treatment with a p38 MAPK inhibitor reverses the barrier defects caused by PLCd 1 downregulation. Interestingly, this treatment also attenuates psoriasis-like skin inflammation in imiquimod-treated mice. These findings demonstrate that PLCd 1 is essential for epidermal barrier integrity. This study also suggests a possible link between PLCd 1 downregulation, p38 MAPK hyperactivation, and barrier defects in psoriasis-like skin inflammation.
- リンク情報
-
- DOI
- https://doi.org/10.1038/cdd.2017.56
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/28430185
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000401701800013&DestApp=WOS_CPL
- URL
- https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019919574&origin=inward
- ID情報
-
- DOI : 10.1038/cdd.2017.56
- ISSN : 1350-9047
- eISSN : 1476-5403
- PubMed ID : 28430185
- SCOPUS ID : 85019919574
- Web of Science ID : WOS:000401701800013