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- Publisher Website: 10.1084/jem.20070462
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- PMID: 17923501
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Article: A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung
Title | A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung |
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Authors | |
Keywords | Molecular Sequence Numbers |
Issue Date | 2007 |
Publisher | Rockefeller University Press. The Journal's web site is located at http://www.jem.org |
Citation | Journal Of Experimental Medicine, 2007, v. 204 n. 11, p. 2529-2536 How to Cite? |
Abstract | Identification of the nature of severe acute respiratory syndrome (SARS)-infected cells is crucial toward understanding the pathogenesis. Using multicolor colocalization techniques, we previously reported that SARS + cells in the lung of fatally infected patients expressed the only known functional receptor, angiotensin-converting enzyme 2, and also a binding receptor, liver/lymph node-specific ICAM-3-grabbing non-integrin (CD209L). In this study, we show that SARS-infected cells also express the stem/progenitor cell markers CD34 and Oct-4, and do not express cytokeratin or surfactant. These putative lung stem/progenitor cells can also be identified in some non-SARS individuals and can be infected by SARS-coronavirus ex vivo. Infection of these cells may contribute to the loss of lung repair capacity that leads to respiratory failure as clinically observed. JEM © The Rockefeller University Press. |
Persistent Identifier | http://hdl.handle.net/10722/132493 |
ISSN | 2023 Impact Factor: 12.6 2023 SCImago Journal Rankings: 6.838 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chen, Y | en_HK |
dc.contributor.author | Chan, VSF | en_HK |
dc.contributor.author | Zheng, B | en_HK |
dc.contributor.author | Chan, KYK | en_HK |
dc.contributor.author | Xu, X | en_HK |
dc.contributor.author | To, LYF | en_HK |
dc.contributor.author | Huang, FP | en_HK |
dc.contributor.author | Khoo, US | en_HK |
dc.contributor.author | Lin, CLS | en_HK |
dc.date.accessioned | 2011-03-28T09:25:22Z | - |
dc.date.available | 2011-03-28T09:25:22Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Journal Of Experimental Medicine, 2007, v. 204 n. 11, p. 2529-2536 | en_HK |
dc.identifier.issn | 0022-1007 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/132493 | - |
dc.description.abstract | Identification of the nature of severe acute respiratory syndrome (SARS)-infected cells is crucial toward understanding the pathogenesis. Using multicolor colocalization techniques, we previously reported that SARS + cells in the lung of fatally infected patients expressed the only known functional receptor, angiotensin-converting enzyme 2, and also a binding receptor, liver/lymph node-specific ICAM-3-grabbing non-integrin (CD209L). In this study, we show that SARS-infected cells also express the stem/progenitor cell markers CD34 and Oct-4, and do not express cytokeratin or surfactant. These putative lung stem/progenitor cells can also be identified in some non-SARS individuals and can be infected by SARS-coronavirus ex vivo. Infection of these cells may contribute to the loss of lung repair capacity that leads to respiratory failure as clinically observed. JEM © The Rockefeller University Press. | en_HK |
dc.language | eng | en_US |
dc.publisher | Rockefeller University Press. The Journal's web site is located at http://www.jem.org | en_HK |
dc.relation.ispartof | Journal of Experimental Medicine | en_HK |
dc.subject | Molecular Sequence Numbers | en_US |
dc.title | A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chan, VSF: sfvchan@hku.hk | en_HK |
dc.identifier.email | Zheng, B: bzheng@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, KYK: kelvinc@pathology.hku.hk | en_HK |
dc.identifier.email | Khoo, US: uskhoo@hku.hk | en_HK |
dc.identifier.authority | Chan, VSF=rp01459 | en_HK |
dc.identifier.authority | Zheng, B=rp00353 | en_HK |
dc.identifier.authority | Chan, KYK=rp00453 | en_HK |
dc.identifier.authority | Khoo, US=rp00362 | en_HK |
dc.description.nature | published_or_final_version | en_US |
dc.identifier.doi | 10.1084/jem.20070462 | en_HK |
dc.identifier.pmid | 17923501 | - |
dc.identifier.pmcid | PMC2118498 | - |
dc.identifier.scopus | eid_2-s2.0-35748954658 | en_HK |
dc.identifier.hkuros | 138878 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-35748954658&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 204 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 2529 | en_HK |
dc.identifier.epage | 2536 | en_HK |
dc.identifier.eissn | 1540-9538 | - |
dc.identifier.isi | WOS:000250652200006 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Chen, Y=16416830300 | en_HK |
dc.identifier.scopusauthorid | Chan, VSF=35200370000 | en_HK |
dc.identifier.scopusauthorid | Zheng, B=7201780588 | en_HK |
dc.identifier.scopusauthorid | Chan, KYK=7406034195 | en_HK |
dc.identifier.scopusauthorid | Xu, X=9276575900 | en_HK |
dc.identifier.scopusauthorid | To, LYF=22954631200 | en_HK |
dc.identifier.scopusauthorid | Huang, FP=35358818300 | en_HK |
dc.identifier.scopusauthorid | Khoo, US=7004195799 | en_HK |
dc.identifier.scopusauthorid | Lin, CLS=37099293900 | en_HK |
dc.identifier.issnl | 0022-1007 | - |