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小鼠巨细胞病毒和人巨细胞病毒在生产性复制过程中对不同细胞类型焦亡诱导作用存在差异。

Murine Cytomegalovirus and Human Cytomegalovirus Differ in Pyroptosis Induction in Different Cell Types During Productive Replication.

作者信息

Carter Jessica J, Schneider Daniel H, Hisamuddin Arshaan M, Dix Richard D

机构信息

Viral Immunology Center, Department of Biology, Georgia State University, Atlanta, GA 30303, USA.

Department of Ophthalmology, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Viruses. 2025 Aug 12;17(8):1106. doi: 10.3390/v17081106.

Abstract

Pyroptosis is a proinflammatory programmed cell death (PCD) that protects the host against invading viruses. We previously reported that pyroptosis plays a prominent role in the pathogenesis of murine cytomegalovirus (MCMV) retinal necrosis using mice with MAIDS as a mouse model for AIDS-related human cytomegalovirus (HCMV) retinal necrosis. Because MCMV and HCMV exhibit species specificity, we sought to determine if pyroptosis induction extends to different cell types of murine or human origin. In vitro studies were therefore performed in which MCMV-infected mouse fibroblasts and mouse macrophages were compared with HCMV-infected human fibroblasts and human ARPE-19 cells for stimulation of caspase-1, gasdermin G (GSDMD), and interleukin (IL)-18 and/or IL-1β transcripts as markers for canonical pyroptosis operation. Whereas MCMV stimulated significant stimulation of pyroptosis-associated transcripts during productive replication of mouse fibroblasts and mouse macrophages, significant stimulation of these transcripts was not detected during HCMV productive replication of human fibroblasts or ARPE-19 cells. Additional studies using UV-inactivated MCMV suggested that virion tegument proteins are not involved in the induction of pyroptosis in MCMV-infected mouse fibroblasts. We conclude that pyroptosis induction during productive replication of MCMV or HCMV is host cell type-dependent and may extend to species specificity, although virus-encoded PCD suppressors must be considered.

摘要

细胞焦亡是一种促炎性程序性细胞死亡(PCD),可保护宿主抵御入侵病毒。我们之前报道,利用患小鼠获得性免疫缺陷综合征(MAIDS)的小鼠作为与艾滋病相关的人类巨细胞病毒(HCMV)视网膜坏死的小鼠模型,细胞焦亡在鼠巨细胞病毒(MCMV)视网膜坏死的发病机制中起重要作用。由于MCMV和HCMV具有种属特异性,我们试图确定细胞焦亡诱导是否扩展到鼠源或人源的不同细胞类型。因此,我们进行了体外研究,将感染MCMV的小鼠成纤维细胞和小鼠巨噬细胞与感染HCMV的人成纤维细胞和人ARPE - 19细胞进行比较,以刺激半胱天冬酶 - 1、gasdermin G(GSDMD)以及白细胞介素(IL)-18和/或IL -1β转录本,作为典型细胞焦亡运作的标志物测定。在小鼠成纤维细胞和小鼠巨噬细胞的有效复制过程中,MCMV显著刺激了与细胞焦亡相关的转录本,而在人成纤维细胞或ARPE - 19细胞的HCMV有效复制过程中,未检测到这些转录本的显著刺激。使用紫外线灭活的MCMV进行的额外研究表明,病毒体被膜蛋白不参与MCMV感染的小鼠成纤维细胞中细胞焦亡的诱导。我们得出结论,MCMV或HCMV有效复制过程中的细胞焦亡诱导依赖于宿主细胞类型,可能还扩展到种属特异性,不过必须考虑病毒编码的PCD抑制因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50a7/12390730/5a64630a0764/viruses-17-01106-g001.jpg

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