Departments of Surgery, University of Illinois College of Medicine at Peoria, Peoria, IL 61605, USA.
Cell Signal. 2013 Oct;25(10):1970-80. doi: 10.1016/j.cellsig.2013.06.003. Epub 2013 Jun 11.
IAPs are a group of regulatory proteins that are structurally related. Their conserved homologues have been identified in various organisms. In human, eight IAP members have been recognized based on baculoviral IAP repeat (BIR) domains. IAPs are key regulators of apoptosis, cytokinesis and signal transduction. The antiapoptotic property of IAPs depends on their professional role for caspases. IAPs are functionally non-equivalent and regulate effector caspases through distinct mechanisms. IAPs impede apoptotic process via membrane receptor-dependent (extrinsic) cascade and mitochondrial dependent (intrinsic) pathway. IAP-mediated apoptosis affects the progression of liver diseases. Therapeutic options of liver diseases may depend on the understanding toward mechanisms of the IAP-mediated apoptosis.
凋亡抑制蛋白(IAPs)是一组结构相关的调节蛋白。它们的保守同源物已在各种生物中被鉴定出来。在人类中,根据杆状病毒 IAP 重复(BIR)结构域,已经识别出 8 种 IAP 成员。IAPs 是细胞凋亡、细胞分裂和信号转导的关键调节剂。IAPs 的抗凋亡特性取决于它们对胱天蛋白酶的专业作用。IAPs 的功能并不等同,它们通过不同的机制调节效应胱天蛋白酶。IAPs 通过膜受体依赖性(外在)级联和线粒体依赖性(内在)途径阻碍凋亡过程。IAP 介导的细胞凋亡影响肝脏疾病的进展。肝脏疾病的治疗选择可能取决于对 IAP 介导的细胞凋亡机制的理解。