The PPARγ agonist rosiglitazone is antifibrotic for scleroderma lung fibroblasts: Mechanisms of action and differential racial effects

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Abstract

We present novel data demonstrating that the expression of PPARγ is reduced in lung fibroblasts from black SSc-ILD patients as compared to white patients. Activating PPARγ with the agonist rosiglitazone increased the expression of MMP-1 and inhibited collagen type I in lung fibroblasts isolated from white, but not black, SSc-ILD patients. Blocking the c-Met receptor abolishes rosiglitazone's effects on collagen and MMP-1 in lung fibroblasts isolated from white SSc-ILD patients, while augmenting the expression of the c-Met receptor in fibroblasts from black SSc-ILD patients replicates the effects of rosiglitazone seen in whites. We conclude that PPARγ agonists warrant consideration as potential antifibrotic drugs in patients with SSc-ILD. Differential therapeutic effects might be anticipated especially relative to racial differences and the functional expression of the c-Met receptor. © 2012 Galina S. Bogatkevich et al.

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Bogatkevich, G. S., Highland, K. B., Akter, T., & Silver, R. M. (2012). The PPARγ agonist rosiglitazone is antifibrotic for scleroderma lung fibroblasts: Mechanisms of action and differential racial effects. Pulmonary Medicine. https://doi.org/10.1155/2012/545172

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