Department of Dermatology, Department of Cellular and Molecular Medicine, Division of Epithelial Biology, University of California, San Diego, La Jolla, CA 92093-0869, USA.
Institute of Precision Medicine, Department of Burns, Department of Dermatology, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, Guangdong, China.
Immunity. 2024 Oct 8;57(10):2296-2309.e5. doi: 10.1016/j.immuni.2024.09.002. Epub 2024 Sep 30.
The surface of the skin is continually exposed to pro-inflammatory stimuli; however, it is unclear why it is not constantly inflamed due to this exposure. Here, we showed undifferentiated keratinocytes residing in the deep epidermis could trigger a strong inflammatory response due to their high expression of pattern recognition receptors (PRRs) that detect damage or pathogens. As keratinocytes differentiated, they migrated outward toward the surface of the skin and decreased their PRR expression, which led to dampened immune responses. ZNF750, a transcription factor expressed only in differentiated keratinocytes, recruited the histone demethylase KDM1A/LSD1 to silence genes coding for PRRs (TLR3, IFIH1/MDA5, and DDX58/RIG1). Loss of ZNF750 or KDM1A in human keratinocytes or mice resulted in sustained and excessive inflammation resembling psoriatic skin, which could be restored to homeostatic conditions upon silencing of TLR3. Our findings explain how the skin's surface prevents excessive inflammation through ZNF750- and KDM1A-mediated suppression of PRRs.
皮肤表面不断暴露于促炎刺激物中;然而,由于这种暴露,皮肤并未持续发炎的原因尚不清楚。在这里,我们发现未分化的角质形成细胞由于其高水平表达的模式识别受体 (PRR) 而能够触发强烈的炎症反应,这些受体可以检测到损伤或病原体。随着角质形成细胞的分化,它们向外迁移到皮肤表面并降低 PRR 的表达,从而导致免疫反应减弱。仅在分化的角质形成细胞中表达的转录因子 ZNF750 募集组蛋白去甲基化酶 KDM1A/LSD1 来沉默编码 PRR (TLR3、IFIH1/MDA5 和 DDX58/RIG1) 的基因。在人类角质形成细胞或小鼠中缺失 ZNF750 或 KDM1A 会导致类似于银屑病皮肤的持续和过度炎症,这种炎症可以通过沉默 TLR3 恢复到稳态条件。我们的研究结果解释了皮肤表面如何通过 ZNF750 和 KDM1A 介导的 PRR 抑制来防止过度炎症。