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G 蛋白偶联受体-Gαi 信号的激活增加角质形成细胞增殖并减少分化,导致表皮过度增生。

Activation of G-Protein Coupled Receptor-Gαi Signaling Increases Keratinocyte Proliferation and Reduces Differentiation, Leading to Epidermal Hyperplasia.

机构信息

Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Moores Cancer Center, University of California, San Diego, La Jolla, California.

出版信息

J Invest Dermatol. 2020 Jun;140(6):1195-1203.e3. doi: 10.1016/j.jid.2019.10.012. Epub 2019 Nov 7.

Abstract

G-protein coupled receptors (GPCRs) and their associated heterotrimeric G proteins impinge on pathways that control epithelial cell self-renewal and differentiation. Although it is known that Gαs protein signaling regulates skin homeostasis in vivo, the role of GPCR-coupled Gαi proteins in the skin is unclear. Here, by using a chemogenetic approach, we demonstrate that GPCR-Gαi activation can regulate keratinocyte proliferation and differentiation and that overactivation of Gαi-signaling in the basal compartment of the mouse skin can lead to epidermal hyperplasia. Our results expand our understanding of the role of GPCR-cAMP signaling in skin homeostasis and reveal overlapping and divergent roles of the cAMP-regulating heterotrimeric Gαs and Gαi proteins in keratinocytes.

摘要

G 蛋白偶联受体(GPCRs)及其相关的异三聚体 G 蛋白作用于控制上皮细胞自我更新和分化的途径。尽管已知 Gαs 蛋白信号转导在体内调节皮肤稳态,但 GPCR 偶联的 Gαi 蛋白在皮肤中的作用尚不清楚。在这里,我们通过使用化学遗传学方法证明,GPCR-Gαi 激活可以调节角质形成细胞的增殖和分化,并且在小鼠皮肤的基底隔室中超激活 Gαi 信号转导可导致表皮过度增生。我们的结果扩展了我们对 GPCR-cAMP 信号转导在皮肤稳态中的作用的理解,并揭示了 cAMP 调节异三聚体 Gαs 和 Gαi 蛋白在角质形成细胞中重叠和不同的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/7202966/17e60bec846c/nihms-1542207-f0001.jpg

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