Li Xiaocui, Hu Xiaofang, You Hongjuan, Zheng Kuiyang, Tang Renxian, Kong Fanyun
Jiangsu Key Laboratory of Immunity and Metabolism, Department of Pathogenic Biology and Immunology, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Department of Breast Surgery, The Second Affiliated Hospital of Shandong First Medical University, Taian, Shandong, China.
iScience. 2024 Dec 20;28(2):111667. doi: 10.1016/j.isci.2024.111667. eCollection 2025 Feb 21.
Pattern recognition receptors (PRRs), consisting of Toll-like receptors, RIG-I-like receptors, cytosolic DNA sensors, and NOD-like receptors, sense exogenous pathogenic molecules and endogenous damage signals to maintain physiological homeostasis. Upon activation, PRRs stimulate the sensitization of nuclear factor κB, mitogen-activated protein kinase, TANK-binding kinase 1-interferon (IFN) regulatory factor, and inflammasome signaling pathways to produce inflammatory factors and IFNs to activate Janus kinase/signal transducer and activator of transcription signaling pathways, resulting in anti-infection, antitumor, and other specific immune responses. Palmitoylation is a crucial type of post-translational modification that reversibly alters the localization, stability, and biological activity of target molecules. Here, we discuss the available knowledge on the biological roles and underlying mechanisms linked to protein palmitoylation in modulating PRRs and their downstream signaling pathways under physiological and pathological conditions. Moreover, recent advances in the use of palmitoylation as an attractive therapeutic target for disorders caused by the dysregulation of PRRs were summarized.
模式识别受体(PRR)由Toll样受体、维甲酸诱导基因I样受体、胞质DNA传感器和NOD样受体组成,可感知外源性致病分子和内源性损伤信号,以维持生理稳态。激活后,PRR刺激核因子κB、丝裂原活化蛋白激酶、TANK结合激酶1-干扰素(IFN)调节因子和炎性小体信号通路的敏化,以产生炎性因子和IFN,从而激活Janus激酶/信号转导子和转录激活子信号通路,引发抗感染、抗肿瘤和其他特异性免疫反应。棕榈酰化是一种关键的翻译后修饰类型,可可逆地改变靶分子的定位、稳定性和生物学活性。在此,我们讨论了在生理和病理条件下,与蛋白质棕榈酰化调节PRR及其下游信号通路相关的生物学作用和潜在机制的现有知识。此外,还总结了将棕榈酰化作为PRR失调所致疾病的有吸引力的治疗靶点的最新进展。