Key result
Platelet-derived growth factor inhibited human adipocyte differentiation, reducing triacylglycerol accumulation by 75% (P<0.01) via an IKKbeta-dependent pathway.
PDGF inhibits human adipocyte differentiation via a novel signaling pathway requiring the pro-inflammatory kinase IKKbeta.
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Hypothesis-generating for PDGF-IKKbeta in adipogenesis; prospective human studies needed before any clinical consideration.
To clarify how anti-adipogenic factors act on preadipocytes to inhibit their differentiation, we compared preadipocyte signaling responses generated by platelet-derived growth factor (PDGF; anti-adipogenic) versus insulin (pro-adipogenic). PDGF, but not insulin, stimulated the phosphorylation of inhibitor of kappaB kinase beta (IKKbeta) in a time-dependent manner. This PDGF-dependent phosphorylation event was inhibited by 60% (P<0.05) when the cells were pretreated with wortmannin, indicating a requirement for the phosphatidylinositol (PI) 3-kinase/AKT pathway. IKKbeta phosphorylation by PDGF was neither accompanied by IkappaBalpha degradation nor NF-kappaB activation. PDGF inhibited human adipocyte differentiation, assessed by triacylglycerol accumulation (75% reduction; P<0.01) and by fatty acid synthase protein expression (60% reduction; P<0.05); these responses were no longer apparent in the presence of sc-514, a selective inhibitor of IKKbeta. Our data describe a novel PDGF response in human preadipocytes that involves the pro-inflammatory kinase IKKbeta and demonstrate that it is required for the inhibition of adipogenesis.
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Gagnon et al. (2009) studied Adipogenesis. Platelet-derived growth factor (PDGF) vs. Insulin was evaluated on Adipocyte differentiation (assessed by triacylglycerol accumulation) (75% reduction, p=<0.01). Platelet-derived growth factor inhibited human adipocyte differentiation, reducing triacylglycerol accumulation by 75% (P<0.01) via an IKKbeta-dependent pathway.
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