A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung

Author:

Chen Yongxiong12,Chan Vera Sau-Fong12,Zheng Bojian3,Chan Kelvin Yuen-Kwong4,Xu Xiaoning5,To Leo Yuk-Fai12,Huang Fang-Ping6,Khoo Ui-Soon4,Lin Chen-Lung Steve12

Affiliation:

1. Department of Surgery,

2. Division of Surgery, Oncology, Reproductive Biology and Anaesthetics, Faculty of Medicine, and

3. Department of Microbiology, and

4. Department of Pathology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China

5. Human Immunology Unit, The Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK

6. Department of Molecular Genetics and Rheumatology, Division of Medicine, Imperial College London, Hammersmith Hospital, London W12 0NN, UK

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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