Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition.

ABSTRACT: There are currently few treatment options for pulmonary fibrosis. Innovations may come from a better understanding of the cellular origin of the characteristic fibrotic lesions. We have analyzed normal and fibrotic mouse and human lungs by confocal microscopy to define stromal cell populations with respect to several commonly used markers. In both species, we observed unexpected heterogeneity of stromal cells. These include numerous cells with molecular and morphological characteristics of pericytes, implicated as a source of myofibroblasts in other fibrotic tissues. We used mouse genetic tools to follow the fates of specific cell types in the bleomcyin-induced model of pulmonary fibrosis. Using inducible transgenic alleles to lineage trace pericyte-like cells in the alveolar interstitium,

SUBMITTER: Rock JR 

PROVIDER: S-EPMC3248478 | biostudies-literature | 2011 Dec

REPOSITORIES: biostudies-literature