Institute of Biological Sciences, Cardinal Stefan Wyszyński University in Warsaw, 01-815 Warsaw, Poland.
Department of Biochemistry and Microbiology, Institute of Biology, Warsaw University of Life Sciences-SGGW, 02-787 Warsaw, Poland.
Int J Mol Sci. 2021 Feb 16;22(4):1956. doi: 10.3390/ijms22041956.
Bcl-xL represents a family of proteins responsible for the regulation of the intrinsic apoptosis pathway. Due to its anti-apoptotic activity, Bcl-xL co-determines the viability of various virally infected cells. Their survival may determine the effectiveness of viral replication and spread, dynamics of systemic infection, and viral pathogenesis. In this paper, we have reviewed the role of Bcl-xL in the context of host infection by eight different RNA and DNA viruses: hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV), influenza A virus (IAV), Epstein-Barr virus (EBV), human T-lymphotropic virus type-1 (HTLV-1), Maraba virus (MRBV), Schmallenberg virus (SBV) and coronavirus (CoV). We have described an influence of viral infection on the intracellular level of Bcl-xL and discussed the impact of Bcl-xL-dependent cell survival control on infection-accompanying pathogenic events such as tissue damage or oncogenesis. We have also presented anti-viral treatment strategies based on the pharmacological regulation of Bcl-xL expression or activity.
Bcl-xL 代表了一类负责调节内在凋亡途径的蛋白质。由于其抗凋亡活性,Bcl-xL 共同决定了各种病毒感染细胞的活力。它们的存活可能决定了病毒复制和传播的有效性、全身感染的动态和病毒发病机制。在本文中,我们回顾了 Bcl-xL 在八种不同的 RNA 和 DNA 病毒宿主感染中的作用:乙型肝炎病毒 (HBV)、丙型肝炎病毒 (HCV)、人类免疫缺陷病毒 (HIV)、甲型流感病毒 (IAV)、爱泼斯坦-巴尔病毒 (EBV)、人类 T 淋巴细胞白血病病毒 1 型 (HTLV-1)、马利巴病毒 (MRBV)、沙米恩贝格病毒 (SBV) 和冠状病毒 (CoV)。我们描述了病毒感染对细胞内 Bcl-xL 水平的影响,并讨论了 Bcl-xL 依赖性细胞存活控制对感染伴随的病理事件(如组织损伤或肿瘤发生)的影响。我们还提出了基于 Bcl-xL 表达或活性的药理学调节的抗病毒治疗策略。