In dividing cells, the RNA-binding protein HuR associates with and stablizes labile mRNAs encoding proliferative proteins, events that are linked to the increased cytoplasmic presence of HuR. Here, assessment of HuR levels in various vascular pathologies (intimal hyperplasia, atherosclerosis and neointimal proliferation, sclerosis of arterialized saphenous venous graft, and fibromuscular dysplasia) revealed a distinct increase in HuR expression and cytoplasmic abundance within the intima and neointima layers. Based on these observations, we postulated a role for HuR in promoting the proliferation of vascular smooth muscle cells (VSMCs). To test this hypothesis directly, we investigated the expression, subcellular localization, and proliferative influence of HuR in human aortic smooth muscle cells (hVSMCs). Treatment of hVSMCs with platelet-derived growth factor (PDGF) increased HuR levels in the cytoplasm, thereby influencing the expression of metabolic, proliferative, and structural genes. Importantly, knockdown of HuR expression by using RNA interference caused a reduction of hVSMC proliferation, both basally and following PDGF treatment. We propose that HuR contributes to regulating hVSMC growth and homeostasis in pathologies associated with vascular smooth muscle proliferation