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食蟹猴感染猴免疫缺陷病毒后空肠和外周组织 SARS-CoV-2 受体 ACE2 及相关蛋白或基因的变化。

Simian Immunodeficiency Virus Infection Mediated Changes in Jejunum and Peripheral SARS-CoV-2 Receptor ACE2 and Associated Proteins or Genes in Rhesus Macaques.

机构信息

Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.

Department of Mathematical Sciences, Michigan Technological University, Houghton, MI, United States.

出版信息

Front Immunol. 2022 Feb 25;13:835686. doi: 10.3389/fimmu.2022.835686. eCollection 2022.

Abstract

Angiotensin converting enzyme-2 (ACE2) and associated proteins play a pivotal role in various physiological and pathological events, such as immune activation, inflammation, gut barrier maintenance, intestinal stem cell proliferation, and apoptosis. Although many of these clinical events are quite significant in SIV/HIV infection, expression profiling of these proteins has not been well reported. Considering the different pathological consequences in the gut after HIV infection, we hypothesized that the expression of ACE2 and associated proteins of the Renin-angiotensin system (RAS) could be compromised after SIV/HIV infection. We quantified the gene expression of as well as , , and , and compared between SIV infected and uninfected rhesus macaques (; hereafter abbreviated RMs). The gene expression analysis revealed significant downregulation of and upregulation of and inflammatory cytokine in the gut of infected RMs. Protein expression profiling also revealed significant upregulation of AGTR2 after infection. The expression of ACE2 in protein level was also decreased, but not significantly, after infection. To understand the entirety of the process in newly regenerated epithelial cells, a global transcriptomic study of enteroids raised from intestinal stem cells was performed. Interestingly, most of the genes associated with the RAS, such as , , , , , were found to be downregulated in SIV infection. was found to be a key regulator of ACE2 and related protein expression. Jejunum CD4+ T cell depletion and increased IL-6 mRNA, MCP-1 and AGTR2 expression may signal inflammation, monocyte/macrophage accumulation and epithelial apoptosis in accelerating SIV pathogenesis. Overall, the findings in the study suggested a possible impact of SIV/HIV infection on expression of ACE2 and RAS-associated proteins resulting in the loss of gut homeostasis. In the context of the current COVID-19 pandemic, the outcome of SARS-CoV-2 and HIV co-infection remains uncertain and needs further investigation as the significance profile of ACE2, a viral entry receptor for SARS-CoV-2, and its expression in mRNA and protein varied in the current study. There is a concern of aggravated SARS-CoV-2 outcomes due to possible serious pathological events in the gut resulting from compromised expression of RAS- associated proteins in SIV/HIV infection.

摘要

血管紧张素转换酶 2(ACE2)和相关蛋白在各种生理和病理事件中发挥着关键作用,如免疫激活、炎症、肠道屏障维持、肠道干细胞增殖和细胞凋亡。尽管这些临床事件在 SIV/HIV 感染中非常重要,但这些蛋白的表达谱尚未得到很好的报道。考虑到 HIV 感染后肠道的不同病理后果,我们假设 SIV/HIV 感染后,肾素-血管紧张素系统(RAS)的 ACE2 和相关蛋白的表达可能会受到损害。我们对 SIV 感染和未感染恒河猴(简称 RMs)的 ACE2 及相关蛋白的基因表达进行了定量分析。基因表达分析显示,感染 RMs 的肠道中 显著下调, 、 和炎症细胞因子 显著上调。蛋白表达谱分析也显示感染后 AGTR2 显著上调。感染后 ACE2 蛋白水平的表达也有所下降,但不显著。为了了解新生上皮细胞的整个过程,我们对从肠道干细胞中培养的类肠器官进行了全转录组研究。有趣的是,大多数与 RAS 相关的基因,如 、 、 、 、 ,在 SIV 感染中发现下调。 被发现是 ACE2 和相关蛋白表达的关键调节因子。空肠 CD4+T 细胞耗竭和 IL-6mRNA、MCP-1 和 AGTR2 表达增加可能导致炎症、单核细胞/巨噬细胞积累和上皮细胞凋亡,加速 SIV 发病机制。总的来说,研究结果表明,SIV/HIV 感染可能对 ACE2 和 RAS 相关蛋白的表达产生影响,导致肠道稳态丧失。在当前 COVID-19 大流行的背景下,SARS-CoV-2 和 HIV 合并感染的结果仍不确定,需要进一步研究,因为在本研究中,SARS-CoV-2 的病毒进入受体 ACE2 及其在 mRNA 和蛋白中的表达的意义谱各不相同。由于 SIV/HIV 感染导致 RAS 相关蛋白表达受损,可能导致肠道发生严重的病理事件,人们担心会加重 SARS-CoV-2 的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb50/8914048/5b28c3d750a6/fimmu-13-835686-g001.jpg

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