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