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极化上皮细胞中血管紧张素转换酶2的分析:表面表达及作为严重急性呼吸综合征相关冠状病毒受体的功能

Analysis of ACE2 in polarized epithelial cells: surface expression and function as receptor for severe acute respiratory syndrome-associated coronavirus.

作者信息

Ren Xiaofeng, Glende Jörg, Al-Falah Marwan, de Vries Victor, Schwegmann-Wessels Christel, Qu Xiuxia, Tan Lei, Tschernig Thomas, Deng Hongkui, Naim Hassan Y, Herrler Georg

机构信息

Institut für Virologie, Tierärztliche Hochschule Hannover, Bünteweg 17, D-30559 Hannover, Germany.

Institut für Physiologische Chemie, Tierärztliche Hochschule Hannover, Bünteweg 17, D-30559 Hannover, Germany.

出版信息

J Gen Virol. 2006 Jun;87(Pt 6):1691-1695. doi: 10.1099/vir.0.81749-0.

Abstract

The primary target of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) is epithelial cells in the respiratory and intestinal tract. The cellular receptor for SARS-CoV, angiotensin-converting enzyme 2 (ACE2), has been shown to be localized on the apical plasma membrane of polarized respiratory epithelial cells and to mediate infection from the apical side of these cells. Here, these results were confirmed and extended by including a colon carcinoma cell line (Caco-2), a lung carcinoma cell line (Calu-3) and Vero E6 cells in our analysis. All three cell types expressed human ACE2 on the apical membrane domain and were infected via this route, as determined with vesicular stomatitis virus pseudotypes containing the S protein of SARS-CoV. In a histological analysis of the respiratory tract, ACE2 was detected in the trachea, main bronchus and alveoli, and occasionally also in the small bronchi. These data will help us to understand the pathogenesis of SARS-CoV infection.

摘要

严重急性呼吸综合征相关冠状病毒(SARS-CoV)的主要靶标是呼吸道和肠道中的上皮细胞。SARS-CoV的细胞受体血管紧张素转换酶2(ACE2)已被证明定位于极化呼吸道上皮细胞的顶端质膜上,并介导这些细胞从顶端侧受到感染。在这里,通过在我们的分析中纳入结肠癌细胞系(Caco-2)、肺癌细胞系(Calu-3)和Vero E6细胞,这些结果得到了证实和扩展。所有这三种细胞类型在顶端膜结构域均表达人ACE2,并通过该途径受到感染,这是用含有SARS-CoV S蛋白的水泡性口炎病毒假型确定的。在呼吸道的组织学分析中,在气管、主支气管和肺泡中检测到了ACE2,偶尔在小支气管中也检测到。这些数据将有助于我们了解SARS-CoV感染的发病机制。

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