Hoss Florian, Rodriguez-Alcazar Juan F, Latz Eicke
Institute of Innate Immunity, University Hospitals, University of Bonn, Sigmund-Freud-Straße 25, 53127, Bonn, Germany.
Department of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, MA, USA.
Cell Mol Life Sci. 2017 Apr;74(7):1211-1229. doi: 10.1007/s00018-016-2396-6. Epub 2016 Oct 19.
The inflammasome adapter ASC links activated inflammasome sensors to the effector molecule pro-caspase-1. Recruitment of pro-caspase-1 to ASC promotes the autocatalytic activation of caspase-1, which leads to the release of pro-inflammatory cytokines, such as IL-1β. Upon triggering of inflammasome sensors, ASC assembles into large helical fibrils that interact with each other serving as a supramolecular signaling platform termed the ASC speck. Alternative splicing, post-translational modifications of ASC, as well as interaction with other proteins can perturb ASC function. In several inflammatory diseases, ASC specks can be found in the extracellular space and its presence correlates with poor prognosis. Here, we review the role of ASC in inflammation, and focus on the structural mechanisms that lead to ASC speck formation, the regulation of ASC function during inflammasome assembly, and the importance of ASC specks in disease.
炎症小体接头蛋白ASC将激活的炎症小体传感器与效应分子前半胱天冬酶-1连接起来。前半胱天冬酶-1招募到ASC会促进半胱天冬酶-1的自催化激活,进而导致促炎细胞因子如IL-1β的释放。炎症小体传感器被触发后,ASC组装成大型螺旋纤维,这些纤维相互作用,形成一个超分子信号平台,称为ASC斑点。ASC的可变剪接、翻译后修饰以及与其他蛋白质的相互作用会扰乱ASC的功能。在几种炎症性疾病中,可在细胞外空间发现ASC斑点,其存在与预后不良相关。在此,我们综述了ASC在炎症中的作用,并重点关注导致ASC斑点形成的结构机制、炎症小体组装过程中ASC功能的调节以及ASC斑点在疾病中的重要性。