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杀伤细胞蛋白酶可以以非细胞毒性的方式靶向病毒即刻早期蛋白,从而控制人类巨细胞病毒感染。

Killer cell proteases can target viral immediate-early proteins to control human cytomegalovirus infection in a noncytotoxic manner.

机构信息

Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Center for Translational Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

PLoS Pathog. 2020 Apr 13;16(4):e1008426. doi: 10.1371/journal.ppat.1008426. eCollection 2020 Apr.

Abstract

Human cytomegalovirus (HCMV) is the most frequent viral cause of congenital defects and can trigger devastating disease in immune-suppressed patients. Cytotoxic lymphocytes (CD8+ T cells and NK cells) control HCMV infection by releasing interferon-γ and five granzymes (GrA, GrB, GrH, GrK, GrM), which are believed to kill infected host cells through cleavage of intracellular death substrates. However, it has recently been demonstrated that the in vivo killing capacity of cytotoxic T cells is limited and multiple T cell hits are required to kill a single virus-infected cell. This raises the question whether cytotoxic lymphocytes can use granzymes to control HCMV infection in a noncytotoxic manner. Here, we demonstrate that (primary) cytotoxic lymphocytes can block HCMV dissemination independent of host cell death, and interferon-α/β/γ. Prior to killing, cytotoxic lymphocytes induce the degradation of viral immediate-early (IE) proteins IE1 and IE2 in HCMV-infected cells. Intriguingly, both IE1 and/or IE2 are directly proteolyzed by all human granzymes, with GrB and GrM being most efficient. GrB and GrM cleave IE1 after Asp398 and Leu414, respectively, likely resulting in IE1 aberrant cellular localization, IE1 instability, and functional impairment of IE1 to interfere with the JAK-STAT signaling pathway. Furthermore, GrB and GrM cleave IE2 after Asp184 and Leu173, respectively, resulting in IE2 aberrant cellular localization and functional abolishment of IE2 to transactivate the HCMV UL112 early promoter. Taken together, our data indicate that cytotoxic lymphocytes can also employ noncytotoxic ways to control HCMV infection, which may be explained by granzyme-mediated targeting of indispensable viral proteins during lytic infection.

摘要

人类巨细胞病毒(HCMV)是先天性缺陷最常见的病毒病因,并且可在免疫抑制患者中引发毁灭性疾病。细胞毒性淋巴细胞(CD8+ T 细胞和 NK 细胞)通过释放干扰素-γ和五种颗粒酶(GrA、GrB、GrH、GrK、GrM)来控制 HCMV 感染,据信这些颗粒酶通过切割细胞内死亡底物来杀死受感染的宿主细胞。然而,最近已经证明,细胞毒性 T 细胞的体内杀伤能力是有限的,并且需要多个 T 细胞打击才能杀死单个病毒感染的细胞。这就提出了一个问题,即细胞毒性淋巴细胞是否可以通过颗粒酶以非细胞毒性方式控制 HCMV 感染。在这里,我们证明(原代)细胞毒性淋巴细胞可以在不依赖宿主细胞死亡和干扰素-α/β/γ的情况下阻断 HCMV 的传播。在杀伤之前,细胞毒性淋巴细胞诱导 HCMV 感染细胞中病毒即刻早期(IE)蛋白 IE1 和 IE2 的降解。有趣的是,所有人类颗粒酶都可以直接蛋白水解 IE1 和/或 IE2,其中 GrB 和 GrM 的效率最高。GrB 和 GrM 分别在 Asp398 和 Leu414 后切割 IE1,可能导致 IE1 异常细胞定位、IE1 不稳定性以及 IE1 功能障碍,从而干扰 JAK-STAT 信号通路。此外,GrB 和 GrM 分别在 Asp184 和 Leu173 后切割 IE2,导致 IE2 异常细胞定位和 IE2 功能丧失,从而激活 HCMV UL112 早期启动子。总之,我们的数据表明,细胞毒性淋巴细胞也可以采用非细胞毒性方式来控制 HCMV 感染,这可以通过在裂解感染期间颗粒酶介导靶向必需病毒蛋白来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ea7/7179929/347985224591/ppat.1008426.g001.jpg

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