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.
Cite
CITATION STYLE
Chen, Y., Chan, V. S. F., Zheng, B., Chan, K. Y. K., Xu, X., To, L. Y. F., … Lin, C. L. S. (2007). A novel subset of putative stem/progenitor CD34+ Oct-4 + cells is the major target for SARS coronavirus in human lung. Journal of Experimental Medicine, 204(11), 2529–2536. https://doi.org/10.1084/jem.20070462
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.