t-0070907 and Carotid-Artery-Diseases

Cardiovascular disease is the leading cause of morbidity and mortality in patients with type 2 diabetes mellitus (T2DM). Pioglitazone, the widely used thiazolidinedione, is shown to be efficient in the prevention of cardiovascular complications of T2DM. In this study, we report that pioglitazone inhibits CXCR7 expression and thus blocks chemotaxis in differentiated macrophage without perturbing cell viability or macrophage differentiation. In addition, pioglitazone-mediated CXCR7 suppression and chemotaxis inhibition occur via activating peroxisome proliferator-activated receptor γ (PPARγ) but not PPARα in differentiated macrophage. More importantly, pioglitazone therapy-induced PPARγ activation suppresses CXCR7 expression in human carotid atherosclerotic lesions. Collectively, our data demonstrate that pioglitazone suppresses CXCR7 expression to inhibit human macrophage chemotaxis through PPARγ.

Topics: Benzamides; Carotid Artery Diseases; Cell Differentiation; Cells, Cultured; Chemotaxis; Combined Modality Therapy; Depression, Chemical; Diabetes Mellitus, Type 2; Down-Regulation; Endarterectomy, Carotid; Gene Expression Regulation; Humans; Macrophages; Pioglitazone; PPAR alpha; PPAR gamma; Pyridines; Receptors, CXCR; RNA Interference; RNA, Small Interfering; Rosiglitazone; Thiazolidinediones