Abstract
Background and Aims : Proliferation of endothelial cells (EC) and smooth muscle cells (SMC) and SMC phenotypic plasticity are critical processes in the development of atherosclerosis. We have previously shown that the sublytic C5b-9 effector Response Gene to Complement-32 (RGC-32) regulates EC proliferation, migration, and cytoskeletal reorganization. Our goal was to explore the effect of RGC-32 on cell cycle activation and TGF-β induced differentiation of SMC and the extracellular matrix (ECM) production.
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