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

被引:140
作者
Ren, Xiaofeng
Glende, Jorg
Al-Falah, Marwan
de Vries, Victor
Schwegmann-Wessels, Christel
Qu, Xiuxia
Tan, Lei
Tschernig, Thomas
Deng, Hongkui
Naim, Hassan Y.
Herrler, Georg
机构
[1] Tierarztlichen Hsch Hannover, Inst Virol, D-30559 Hannover, Germany
[2] Tierarztlichen Hsch Hannover, Inst Physiol Chem, D-30559 Hannover, Germany
[3] Hannover Med Sch, Inst Funkt & Angew Anat, D-30625 Hannover, Germany
[4] Peking Univ, Coll Life Sci, Dept Cell Biol & Genet, Beijing 100871, Peoples R China
关键词
D O I
10.1099/vir.0.81749-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
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.
引用
收藏
页码:1691 / 1695
页数:5
相关论文
共 17 条
[1]
Compans RW, 2005, MUCOSAL IMMUNOLOGY, 3RD EDITION, P769, DOI 10.1016/B978-012491543-5/50045-0
[2]
AMINOPEPTIDASE-N IS A MAJOR RECEPTOR FOR THE ENTEROPATHOGENIC CORONAVIRUS TGEV [J].
DELMAS, B ;
GELFI, J ;
LHARIDON, R ;
VOGEL, LK ;
SJOSTROM, H ;
NOREN, O ;
LAUDE, H .
NATURE, 1992, 357 (6377) :417-420
[3]
Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis [J].
Hamming, I ;
Timens, W ;
Bulthuis, MLC ;
Lely, AT ;
Navis, GJ ;
van Goor, H .
JOURNAL OF PATHOLOGY, 2004, 203 (02) :631-637
[4]
Use of influenza C virus glycoprotein HEF for generation of vesicular stomatitis virus pseudotypes [J].
Hanika, A ;
Larisch, B ;
Steinmann, E ;
Schwegmann-Wessels, C ;
Herrler, G ;
Zimmer, G .
JOURNAL OF GENERAL VIROLOGY, 2005, 86 :1455-1465
[5]
Human coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry [J].
Hofmann, H ;
Pyrc, K ;
van der Hoek, L ;
Geier, M ;
Berkhout, B ;
Pöhlmann, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (22) :7988-7993
[6]
ACE2 receptor expression and severe acute respiratory syndrome coronavirus infection depend on differentiation of human airway epithelia [J].
Jia, HP ;
Look, DC ;
Shi, L ;
Hickey, M ;
Pewe, L ;
Netland, J ;
Farzan, M ;
Wohlford-Lenane, C ;
Perlman, S ;
McCray, PB .
JOURNAL OF VIROLOGY, 2005, 79 (23) :14614-14621
[7]
Point mutations in the S protein connect the sialic acid binding activity with the enteropathogenicity of transmissible gastroenteritis coronavirus [J].
Krempl, C ;
Schultze, B ;
Laude, H ;
Herrler, G .
JOURNAL OF VIROLOGY, 1997, 71 (04) :3285-3287
[8]
Leung WK, 2003, GASTROENTEROLOGY, V125, P1011, DOI [10.1053/S0016-5085(03)01215-0, 10.1016/j.gastro.2003.08.001]
[9]
Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus [J].
Li, WH ;
Moore, MJ ;
Vasilieva, N ;
Sui, JH ;
Wong, SK ;
Berne, MA ;
Somasundaran, M ;
Sullivan, JL ;
Luzuriaga, K ;
Greenough, TC ;
Choe, H ;
Farzan, M .
NATURE, 2003, 426 (6965) :450-454
[10]
Highly infectious SARS-CoV pseudotyped virus reveals the cell tropism and its correlation with receptor expression [J].
Nie, YC ;
Wang, PG ;
Shi, XL ;
Wang, GW ;
Chen, J ;
Zheng, AH ;
Wang, W ;
Wang, Z ;
Qu, XX ;
Luo, M ;
Tan, L ;
Song, XJ ;
Yin, XL ;
Chen, JG ;
Ding, MX ;
Deng, HK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 321 (04) :994-1000