Laboratory for Cytokine Regulation, Center for Integrative Medical Science (IMS), RIKEN Yokohama Institute, Yokohama, Japan.
Laboratory for Integrated Cellular Systems, Center for Integrative Medical Science (IMS), RIKEN Yokohama Institute, Yokohama, Japan.
Front Immunol. 2021 Nov 11;12:663177. doi: 10.3389/fimmu.2021.663177. eCollection 2021.
Dominant-negative mutations associated with signal transducer and activator of transcription 3 (STAT3) signaling, which controls epithelial proliferation in various tissues, lead to atopic dermatitis in hyper IgE syndrome. This dermatitis is thought to be attributed to defects in STAT3 signaling in type 17 helper T cell specification. However, the role of STAT3 signaling in skin epithelial cells remains unclear. We found that STAT3 signaling in keratinocytes is required to maintain skin homeostasis by negatively controlling the expression of hair follicle-specific keratin genes. These expression patterns correlated with the onset of dermatitis, which was observed in specific pathogen-free conditions but not in germ-free conditions, suggesting the involvement of Toll-like receptor-mediated inflammatory responses. Thus, our study suggests that STAT3-dependent gene expression in keratinocytes plays a critical role in maintaining the homeostasis of skin, which is constantly exposed to microorganisms.
与信号转导子和转录激活子 3(STAT3)信号传导相关的显性负突变,控制着各种组织中的上皮细胞增殖,导致高 IgE 综合征中的特应性皮炎。这种皮炎被认为归因于 17 型辅助 T 细胞特异性中 STAT3 信号传导的缺陷。然而,STAT3 信号传导在皮肤上皮细胞中的作用仍不清楚。我们发现,角质形成细胞中的 STAT3 信号传导通过负调控毛囊特异性角蛋白基因的表达来维持皮肤的内稳态。这些表达模式与皮炎的发病相关,在特定病原体条件下观察到,但在无菌条件下没有观察到,表明涉及 Toll 样受体介导的炎症反应。因此,我们的研究表明,角质形成细胞中 STAT3 依赖性基因表达在维持不断暴露于微生物的皮肤内稳态中起着关键作用。