Department of Pathology and Laboratory Medicine, Cedars Sinai, Los Angeles, CA 90048, USA.
Department of Biomedical Sciences, and Samuel Oschin Comprehensive Cancer Institute, Cedars Sinai, Los Angeles, CA 90048, USA.
Int J Mol Sci. 2020 Sep 20;21(18):6901. doi: 10.3390/ijms21186901.
Inflammasomes are protein scaffolds required for the activation of caspase-1 and the subsequent release of interleukin (IL)-1β, IL-18, and danger signals, as well as the induction of pyroptotic cell death to restore homeostasis following infection and sterile tissue damage. However, excessive inflammasome activation also causes detrimental inflammatory disease. Therefore, extensive control mechanisms are necessary to prevent improper inflammasome responses and inflammatory disease. Inflammasomes are assembled by sequential nucleated polymerization of Pyrin domain (PYD) and caspase recruitment domain (CARD)-containing inflammasome components. Once polymerization is nucleated, this process proceeds in a self-perpetuating manner and represents a point of no return. Therefore, regulation of this key step is crucial for a controlled inflammasome response. Here, we provide an update on two single domain protein families containing either a PYD or a CARD, the PYD-only proteins (POPs) and CARD-only proteins (COPs), respectively. Their structure allows them to occupy and block access to key protein-protein interaction domains necessary for inflammasome assembly, thereby regulating the threshold of these nucleated polymerization events, and consequently, the inflammatory host response.
炎性小体是一种蛋白支架,对于 caspase-1 的激活以及随后白细胞介素(IL)-1β、IL-18 和危险信号的释放,以及焦亡性细胞死亡的诱导以在感染和无菌组织损伤后恢复体内平衡是必需的。然而,过度的炎性小体激活也会导致有害的炎症性疾病。因此,需要广泛的控制机制来防止不当的炎性小体反应和炎症性疾病。炎性小体通过含 Pyrin 结构域(PYD)和衔接蛋白募集结构域(CARD)的炎性小体成分的顺序核化聚合组装而成。一旦聚合被引发,这个过程就会以自我维持的方式进行,并且是不可逆转的。因此,对这个关键步骤的调节对于控制炎性小体反应至关重要。在这里,我们提供了两个包含 PYD 或 CARD 的单结构域蛋白家族的最新信息,分别是 PYD 蛋白(POPs)和 CARD 蛋白(COPs)。它们的结构使它们能够占据并阻止关键蛋白-蛋白相互作用结构域的进入,从而调节这些核化聚合事件的阈值,进而调节炎症反应。