刺
干扰素基因刺激剂
信号转导
疾病
先天免疫系统
生物
免疫系统
免疫学
干扰素
医学
计算生物学
细胞生物学
工程类
病理
航空航天工程
作者
Jun Liu,Ke Rui,Na Peng,Hui Luo,Bo Zhu,Xiaoxia Zuo,Liwei Lu,Jixiang Chen,Jie Tian
标识
DOI:10.1016/j.cytogfr.2022.09.003
摘要
Recent studies have illustrated the functional significance of DNA recognition in the activation of innate immune responses among a variety of diseases. The cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway has been found to be modulated by post-translational modifications and can regulate the immune response via type I IFNs. Accumulating evidence indicates a pivotal role of cGAS-STING signaling, being protective or pathogenic, in the development of diseases. Thus, a comprehensive understanding of the post-translational modifications of cGAS-STING pathway and their role in disease development will provide insights in predicting individual disease outcomes and developing appropriate therapies. In this review, we will discuss the regulation of the cGAS-STING pathway and its implications in disease pathologies, as well as pharmacologic strategies to target the cGAS-STING pathway for therapeutic intervention.
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