Department of Cell Biology and Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Trends Immunol. 2014 Feb;35(2):88-93. doi: 10.1016/j.it.2013.10.010. Epub 2013 Dec 2.
STING (STimulator of INterferon Genes) has recently been identified as being essential for controlling host defense countermeasures triggered by microbial cytosolic DNA and subsequently cyclic dinucleotides (CDNs). However, chronic STING activation may also be responsible for initiating certain inflammatory diseases manifested by self DNA. Recent studies have also revealed a key role for cyclic GMP-AMP synthase (cGAS) in STING activation. Although a full understanding of the mechanisms of STING activation requires further studies, new insights into STING function afford the opportunity of designing novel compounds aimed at facilitating vaccine development or new therapies for the treatment of inflammatory disease.
STING(干扰素基因刺激物)最近被确定为控制微生物细胞质 DNA 触发的宿主防御反应和随后的环二核苷酸(CDNs)所必需的。然而,慢性 STING 激活也可能导致某些自身 DNA 表现的炎症性疾病的发生。最近的研究还揭示了环状 GMP-AMP 合酶(cGAS)在 STING 激活中的关键作用。尽管进一步研究需要充分了解 STING 激活的机制,但对 STING 功能的新认识为设计旨在促进疫苗开发或治疗炎症性疾病的新疗法的新型化合物提供了机会。