The replication of a mouse adapted SARS-CoV in a mouse cell line stably expressing the murine SARS-CoV receptor mACE2 efficiently induces the expression of proinflammatory cytokines.
The replication of a mouse adapted SARS-CoV in a mouse cell line stably expressing the murine SARS-CoV receptor mACE2 efficiently induces the expression of proinflammatory cytokines.
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DOI:
10.1016/j.jviromet.2013.07.039
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发表时间:
2013-11
影响因子:
3.1
通讯作者:
DeDiego ML
中科院分区:
文献类型:
--
作者:
Regla-Nava JA;Jimenez-Guardeño JM;Nieto-Torres JL;Gallagher TM;Enjuanes L;DeDiego ML
Delayed brain tumor (DBT) mouse cell lines stably expressing the murine angiotensin converting enzyme 2 (mACE2) have been generated. The cell lines are highly susceptible to mouse-adapted SARS-CoV infection. SARS-CoV-MA15 efficiently induced the expression of proinflammatory cytokines and IFN-β in DBT-mACE2 cells. DBT-mACE2 cells provide a good experimental system that is species-homologous to the in vivo systems for evaluating SARS-CoV-host interaction studies. Infection of conventional mice with a mouse adapted (MA15) severe acute respiratory syndrome (SARS) coronavirus (CoV) reproduces many aspects of human SARS such as pathological changes in lung, viremia, neutrophilia, and lethality. However, established mouse cell lines highly susceptible to mouse-adapted SARS-CoV infection are not available. In this work, efficiently transfectable mouse cell lines stably expressing the murine SARS-CoV receptor angiotensin converting enzyme 2 (ACE2) have been generated. These cells yielded high SARS-CoV-MA15 titers and also served as excellent tools for plaque assays. In addition, in these cell lines, SARS-CoV-MA15 induced the expression of proinflammatory cytokines and IFN-β, mimicking what has been observed in experimental animal models infected with SARS-CoV and SARS patients. These cell lines are valuable tools to perform in vitro studies in a mouse cell system that reflects the species used for in vivo studies of SARS-CoV-MA15 pathogenesis.
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DOI:
10.1016/s0140-6736(03)13967-0
发表时间:
2003-07-26
期刊:
Lancet (London, England)
影响因子:
--
作者:
Kuiken T;Fouchier RA;Schutten M;Rimmelzwaan GF;van Amerongen G;van Riel D;Laman JD;de Jong T;van Doornum G;Lim W;Ling AE;Chan PK;Tam JS;Zambon MC;Gopal R;Drosten C;van der Werf S;Escriou N;Manuguerra JC;Stöhr K;Peiris JS;Osterhaus AD
通讯作者:
Osterhaus AD
影响因子:
5.4
作者:
Gosert, R;Kanjanahaluethai, A;Baker, SC
通讯作者:
Baker, SC
影响因子:
2.7
作者:
Hattermann, K;Müller, MA;Niedrig, M
通讯作者:
Niedrig, M
影响因子:
5.4
作者:
Kopecky-Bromberg, Sarah A.;Martinez-Sobrido, Luis;Palese, Peter
通讯作者:
Palese, Peter
影响因子:
5
作者:
Frieman, Matthew;Heise, Mark;Baric, Ralph
通讯作者:
Baric, Ralph