Zhang H M, Cheung P, Yanagawa B, McManus B M, Yang D C
Department of Pathology and Laboratory Medicine, MRL/The iCAPTUR4E Centre, University of British Columbia-St. Paul's Hospital, 1081 Burrard Street, Vancouver, British Columbia, Canada V6Z 1Y6.
Apoptosis. 2003 Jun;8(3):229-36. doi: 10.1023/a:1023616620970.
BNip (formerly known as Nip) proteins, including homologues isolated from human, mouse and Caenorhabditis. elegans, are a relatively new subgroup of the Bcl-2 family. These proteins are classified into this family based on limited sequence homology with the Bcl-2 homology domain 3 and carboxyl terminal transmembrane domain. BNip proteins were first discovered based on their interaction with the adenovirus E1B 19 kDa/Bcl-2 family protein and since then, their roles in cell death pathways have been actively studied. However, the precise mechanisms by which the BNip proteins induce apoptosis and/or necrosis remain to be determined. To advance our knowledge, we have provided a summary and review of current literature regarding BNip proteins including comparative sequence analysis, mutational mapping of the functional domains, and cell death mechanisms involving disruption of mitochondrial homeostasis. Since BNip proteins are expressed at high levels in the heart as compared to other organs, their roles in cardiomyocyte injury during hypoxia or viral infection is a focus of this review. Finally, we discuss potential directions for further study on this increasingly important group of pro-apoptotic proteins.
BNip(以前称为Nip)蛋白,包括从人、小鼠和秀丽隐杆线虫中分离出的同源物,是Bcl-2家族中一个相对较新的亚组。这些蛋白基于与Bcl-2同源结构域3和羧基末端跨膜结构域的有限序列同源性而被归类到这个家族。BNip蛋白最初是基于它们与腺病毒E1B 19 kDa/Bcl-2家族蛋白的相互作用而被发现的,从那时起,它们在细胞死亡途径中的作用就一直被积极研究。然而,BNip蛋白诱导凋亡和/或坏死的确切机制仍有待确定。为了增进我们的了解,我们对当前关于BNip蛋白的文献进行了总结和综述,包括比较序列分析、功能结构域的突变定位以及涉及线粒体稳态破坏的细胞死亡机制。由于与其他器官相比,BNip蛋白在心脏中高水平表达,它们在缺氧或病毒感染期间心肌细胞损伤中的作用是本综述的重点。最后,我们讨论了对这一越来越重要的促凋亡蛋白组进行进一步研究的潜在方向。