[PDF][PDF] A PDGFRα-mediated switch toward CD9high adipocyte progenitors controls obesity-induced adipose tissue fibrosis

G Marcelin, A Ferreira, Y Liu, M Atlan… - Cell metabolism, 2017 - cell.com
G Marcelin, A Ferreira, Y Liu, M Atlan, J Aron-Wisnewsky, V Pelloux, Y Botbol, M Ambrosini…
Cell metabolism, 2017cell.com
Obesity-induced white adipose tissue (WAT) fibrosis is believed to accelerate WAT
dysfunction. However, the cellular origin of WAT fibrosis remains unclear. Here, we show
that adipocyte platelet-derived growth factor receptor-α-positive (PDGFRα+) progenitors
adopt a fibrogenic phenotype in obese mice prone to visceral WAT fibrosis. More
specifically, a subset of PDGFRα+ cells with high CD9 expression (CD9 high) originates pro-
fibrotic cells whereas their CD9 low counterparts, committed to adipogenesis, are almost …
Summary
Obesity-induced white adipose tissue (WAT) fibrosis is believed to accelerate WAT dysfunction. However, the cellular origin of WAT fibrosis remains unclear. Here, we show that adipocyte platelet-derived growth factor receptor-α-positive (PDGFRα+) progenitors adopt a fibrogenic phenotype in obese mice prone to visceral WAT fibrosis. More specifically, a subset of PDGFRα+ cells with high CD9 expression (CD9high) originates pro-fibrotic cells whereas their CD9low counterparts, committed to adipogenesis, are almost completely lost in the fibrotic WAT. PDGFRα pathway activation promotes a phenotypic shift toward PDGFRα+CD9high fibrogenic cells, driving pathological remodeling and altering WAT function in obesity. These findings translated to human obesity as the frequency of CD9high progenitors in omental WAT (oWAT) correlates with oWAT fibrosis level, insulin-resistance severity, and type 2 diabetes. Collectively, our data demonstrate that in addition to representing a WAT adipogenic niche, different PDGFRα+ cell subsets modulate obesity-induced WAT fibrogenesis and are associated with loss of metabolic fitness.
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