Alpha-actinins are critical components of the actin cytoskeleton. Here we show that α-actinins serve another important biological function by binding to and competitively inhibiting calcium-dependent activation of endothelial NOS (eNOS). α-actinin-2 was found to associate with eNOS in a yeast twohybrid screen. In vascular endothelial cells, which only express α-actinin-1 and -4, α-actinin-4 interacted and colocalized with eNOS. Addition of α-actinin-4 directly inhibited eNOS recombinant protein, and overexpression of α-actinin-4 inhibited eNOS activity in eNOS-transfected COS-7 cells and bovine aortic endothelial cells (BAECs). In contrast, knockdown of α-actinin-4 by siRNA increased eNOS activity in BAECs. The α-actinin-4-binding site on eNOS was mapped to a central region comprising the calmodulin-binding domain, and the eNOS-binding site on α-actinin-4 was mapped to the fourth spectrin-like rod domain, R4. Treatment of endothelial cells with a calcium ionophore, A23187, decreased α-actinin-4-eNOS interaction, leading to translocation of α-actinin-4 from plasma membrane to cytoplasm. Indeed, addition of calmodulin displaced α-actinin-4 binding to eNOS and increased eNOS activity. These findings indicate that eNOS activity in vascular endothelial cells is tonically and dynamically regulated by competitive interaction with α-actinin-4 and calmodulin. Keywords endothelium; nitric oxide; ionophore Endothelium-derived NO is an important mediator of vascular function (1). NO is generated from the conversion of L-arginine to L-citrulline by endothelial NOS (eNOS or NOS3). Because of its critical role in vascular homeostasis, eNOS is tightly regulated posttranslationally by several factors. Lipid modifications such as myristoylation or palmitoylation are important to anchor eNOS at the cell membrane, in close proximity to its cofactors and modulators (2). Upstream modulators include protein kinases, which activate eNOS through phosphorylation at Ser-1177 and Ser-635 or inhibit eNOS through phosphorylation at Thr-495 and Ser-116 3 . In particular, Ser-1177 phosphorylation of eNOS by protein kinase B/Akt enhances both basal and agonist-mediated eNOS activity (4,5). In contrast, S-nitrosylation of eNOS renders eNOS inactive under basal conditions (6,7).