Division of Protein and Nucleic Acid Chemistry, Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):12397-401. doi: 10.1073/pnas.1301918110. Epub 2013 Jul 9.
Host species have evolved mechanisms that can inhibit pathogen replication even after a cell has been successfully invaded. Here we show that tripartite-motif protein 21 (TRIM21), a ubiquitously expressed E3 ubiquitin ligase that targets viruses inside the cytosol, protects mice against fatal viral infection. Upon infection with mouse adenovirus-1, naive mice lacking TRIM21 succumb to encephalomyelitis within 7 d. In contrast, wild-type mice rapidly up-regulate TRIM21 and control viremia. Trim21 heterozygous mice have a haploinsufficiency phenotype in which reduced TRIM21 expression leads to a viral load that is higher than wild types but lower than knockouts. TRIM21 is a high-affinity antibody receptor that allows antibodies to operate inside an infected cell. In passive transfer experiments at high viral dose, antisera that fully protects wild-type mice fails to protect most Trim21 knockout animals. These results demonstrate that TRIM21 provides potent antiviral protection and forms an important part of the humoral immune response.
宿主物种已经进化出了一些机制,即使细胞已经被成功入侵,这些机制也可以抑制病原体的复制。在这里,我们表明,三肽基序蛋白 21(TRIM21)是一种广泛表达的细胞质内靶向病毒的 E3 泛素连接酶,可保护小鼠免受致命病毒感染。在感染小鼠腺病毒-1 后,缺乏 TRIM21 的新生小鼠在 7 天内死于脑脊髓炎。相比之下,野生型小鼠迅速上调 TRIM21 并控制病毒血症。Trim21 杂合子小鼠表现出半显性表型,其中 TRIM21 表达减少导致病毒载量高于野生型但低于敲除型。TRIM21 是一种高亲和力的抗体受体,允许抗体在感染细胞内发挥作用。在高病毒剂量的被动转移实验中,完全保护野生型小鼠的抗血清未能保护大多数 Trim21 敲除动物。这些结果表明,TRIM21 提供了强大的抗病毒保护作用,并形成了体液免疫反应的重要组成部分。