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J Gen Virol 87 (2006), 1691-1695; DOI 10.1099/vir.0.81749-0

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© 2006 Society for General Microbiology

Short Communication

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

Xiaofeng Ren1, Jörg Glende1, Marwan Al-Falah2, Victor de Vries3, Christel Schwegmann-Wessels1, Xiuxia Qu4, Lei Tan4, Thomas Tschernig3, Hongkui Deng4, Hassan Y. Naim2 and Georg Herrler1

1 Institut für Virologie, Tierärztliche Hochschule Hannover, Bünteweg 17, D-30559 Hannover, Germany
2 Institut für Physiologische Chemie, Tierärztliche Hochschule Hannover, Bünteweg 17, D-30559 Hannover, Germany
3 Institut für funktionelle und angewandte Anatomie, Medizinische Hochschule Hannover, Carl-Neuberg-Straße, D-30625 Hannover, Germany
4 Department of Cell Biology and Genetics, College of Life Sciences, Peking University, Beijing 100871, People's Republic of China

Correspondence
Georg Herrler
Georg.Herrler{at}tiho-hannover.de

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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