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Publication : Regulation of fibroblast lipid storage and myofibroblast phenotypes during alveolar septation in mice.

First Author  McGowan SE Year  2014
Journal  Am J Physiol Lung Cell Mol Physiol Volume  307
Issue  8 Pages  L618-31
PubMed ID  25150063 Mgi Jnum  J:222204
Mgi Id  MGI:5644121 Doi  10.1152/ajplung.00144.2014
Citation  McGowan SE, et al. (2014) Regulation of fibroblast lipid storage and myofibroblast phenotypes during alveolar septation in mice. Am J Physiol Lung Cell Mol Physiol 307(8):L618-31
abstractText  Signaling through platelet-derived growth factor receptor-alpha (PDGFRalpha) is required for alveolar septation and participates in alveolar regeneration after pneumonectomy. In both adipose tissue and skeletal muscle, bipotent pdgfralpha-expressing progenitors expressing delta-like ligand-1 or sex-determining region Y box 9 (Sox9) may differentiate into either lipid storage cells or myofibroblasts. We analyzed markers of mesenchymal progenitors and differentiation in lung fibroblasts (LF) with different levels (absent, low, or high) of pdgfralpha gene expression. A larger proportion of pdgfralpha-expressing than nonexpressing LF contained Sox9. Neutral lipids, CD166, and Tcf21 were more abundant in LF with a lower compared with a higher level of pdgfralpha gene expression. PDGF-A increased Sox9 in primary LF cultures, suggesting that active signaling through PDGFRalpha is required to maintain Sox9. As alveolar septation progresses from postnatal day (P) 8 to P12, fewer pdgfralpha-expressing LF contain Sox9, whereas more of these LF contain myocardin-like transcription factor-A, showing that Sox9 diminishes as LF become myofibroblasts. At P8, neutral lipid droplets predominate in LF with the lower level of pdgfralpha gene expression, whereas transgelin (tagln) was predominantly expressed in LF with higher pdgfralpha gene expression. Targeted deletion of pdgfralpha in LF, which expressed tagln, reduced Sox9 in alpha-actin (alpha-SMA, ACTA2)-containing LF, whereas it increased the abundance of cell surface delta-like protein-1 (as well as peroxisome proliferator-activated receptor-gamma and tcf21 mRNA in LF, which also expressed stem cell antigen-1). Thus pdgfralpha deletion differentially alters delta-like protein-1 and Sox9, suggesting that targeting different downstream pathways in PDGF-A-responsive LF could identify strategies that promote lung regeneration without initiating fibrosis.
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