CNRS, ImmunoConcEpT, UMR 5164, University Bordeaux, 33000 Bordeaux, France.
Centre National de Référence Maladie Auto-Immune et Systémique Rares Est/Sud-Ouest (RESO), Bordeaux University Hospital, 33076 Bordeaux, France.
Cells. 2022 Apr 24;11(9):1438. doi: 10.3390/cells11091438.
Study of the initial steps of the CD95-mediated signaling pathways is a field of intense research and a long list of actors has been described in the literature. Nonetheless, the dynamism of protein-protein interactions (PPIs) occurring in the presence or absence of its natural ligand, CD95L, and the cellular distribution where these PPIs take place render it difficult to predict what will be the cellular outcome associated with the receptor engagement. Accordingly, CD95 stimulation can trigger apoptosis, necroptosis, pyroptosis, or pro-inflammatory signaling pathways such as nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and phosphatidylinositol-3-kinase (PI3K). Recent data suggest that CD95 can also activate pattern recognition receptors (PRRs) known to sense damage-associated molecular patterns (DAMPs) such as DNA debris and dead cells. This activation might contribute to the pro-inflammatory role of CD95 and favor cancer development or severity of chronic inflammatory and auto-immune disorders. Herein, we discuss some of the molecular links that might connect the CD95 signaling to DAMP sensors.
研究 CD95 介导的信号通路的初始步骤是一个研究热点,文献中已经描述了一长串的参与者。尽管如此,在存在或不存在其天然配体 CD95L 的情况下,蛋白质-蛋白质相互作用(PPIs)的动态性以及这些 PPIs 发生的细胞分布使得很难预测与受体结合相关的细胞结果。因此,CD95 刺激可以触发细胞凋亡、坏死性凋亡、细胞焦亡或促炎信号通路,如核因子 kappa-轻链增强子的 B 细胞(NF-κB)和磷脂酰肌醇-3-激酶(PI3K)。最近的数据表明,CD95 还可以激活已知能够识别损伤相关分子模式(DAMPs)的模式识别受体(PRRs),如 DNA 碎片和死亡细胞。这种激活可能有助于 CD95 的促炎作用,并有利于癌症的发展或慢性炎症和自身免疫性疾病的严重程度。本文中,我们讨论了一些可能将 CD95 信号与 DAMPs 传感器连接起来的分子联系。