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Published ahead of print on March 29, 2007, doi:10.1165/rcmb.2006-0386OC
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American Journal of Respiratory Cell and Molecular Biology. Vol. 37, pp. 152-159, 2007
© 2007 American Thoracic Society
DOI: 10.1165/rcmb.2006-0386OC

Isolation of an Adult Mouse Lung Mesenchymal Progenitor Cell Population

Ross Summer, Kathleen Fitzsimmons, Daniel Dwyer, Jaime Murphy and Alan Fine

The Pulmonary Center, Boston University School of Medicine, Boston, Massachusetts

Correspondence and requests for reprints should be addressed to Ross Summer, The Pulmonary Center, R-304, Boston University School of Medicine, 80 East Concord St., Boston, MA 02118. E-mail: rsummer{at}bu.edu

Contained within the adult lung are differentiated mesenchymal cell types (cartilage, smooth muscle, and myofibrobasts) that provide structural support for airways and vessels. Alterations in the number and phenotype of these cells figure prominently in the pathogenesis of a variety of lung diseases. While these cells are thought to arise locally, progenitors have yet to be purified. In previous work, we developed a method for isolating progenitors from lung tissue: this technique takes advantage of the unique ability of cell populations enriched for somatic stem and progenitor activity to efflux the vital dye Hoechst 33342, a feature that permits isolation by flow cytometry-based procedures. Using this method, we determined that a rare population of mesenchymal progenitors resides within the CD45– CD31– Hoechst low fraction of the adult murine lung. Similar to other mesenchymal progenitors, these cells express Sca-1, CD106, and CD44; can be serially passaged; and can differentiate to smooth muscle, cartilage, bone, and fat. Overall, these findings demonstrate that a phenotypically distinct mesenchymal progenitor resides within the adult murine lung, and provide a scheme for their isolation and study.

Key Words: mesenchymal • progenitors • lung


CLINICAL RELEVANCE

This article is the first to identify and characterize mesenchymal progenitors in the murine lung. These findings have broad implications for understanding lung development and diseases characterized by the accumulation of mesenchymal elements.

 



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