Analysis of ACE2 in polarized epithelial cells: surface expression and function as receptor for severe acute respiratory syndrome-associated coronavirus
Author(s) -
Xiaofeng Ren,
Jörg Glende,
Marwan Alfalah,
Victor de Vries,
Christel SchwegmannWeßels,
Xiuxia Qu,
Lei Tan,
Thomas Tschernig,
Hongkui Deng,
Hassan Y. Naim,
Georg Herrler
Publication year - 2006
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.81749-0
Subject(s) - vero cell , biology , coronavirus , respiratory tract , respiratory system , bronchus , cell culture , pathogenesis , virology , epithelium , lung , receptor , virus , immunology , pathology , respiratory disease , medicine , covid-19 , anatomy , biochemistry , genetics , disease , infectious disease (medical specialty)
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.
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