Background Diabetic nephropathy (dNP), now the leading cause of ESKD, lacks efficient therapies. Coagulation protease-dependent signaling modulates dNP, in part via the G protein-coupled, protease-activated receptors (PARs). Specifically, the cytoprotective protease-activated protein C (aPC) protects from dNP, but the mechanisms are not clear. Methods A combination of in vitro approaches and mouse models evaluated the role of aPC-integrin interaction and related signaling in dNP. Results The zymogen protein C and aPC bind to podocyte integrin-beta(3), a subunit of integrin-alpha(v)beta(3). Deficiency of this integrin impairs thrombin-mediated generation of aPC on podocytes. The interaction of aPC with integrin-alpha(v)beta(3) induces transient binding of integrin-beta(3) with G(alpha 13) and controls PAR-dependent RhoA signaling in podocytes. Binding of aPC to integrin-beta(3) via its RGD sequence is required for the temporal restriction of RhoA signaling in podocytes. In podocytes lacking integrin-beta(3), aPC induces sustained RhoA activation, mimicking the effect of thrombin. In vivo, overexpression of wild-type aPC suppresses pathologic renal RhoA activation and protects against dNP. Disrupting the aPC-integrin-beta(3) interaction by specifically deleting podocyte integrin-beta(3) or by abolishing aPC's integrin-binding RGD sequence enhances RhoA signaling in mice with high aPC levels and abolishes aPC's nephroprotective effect. Pharmacologic inhibition of PAR1, the pivotal thrombin receptor, restricts RhoA activation and nephroprotects RGE-aPC(high) and wild-type mice. Conclusions aPC-integrin-alpha(v)beta(3) acts as a rheostat, controlling PAR1-dependent RhoA activation in podocytes in diabetic nephropathy. These results identify integrin-alpha(v)beta(3) as an essential coreceptor for aPC that is required for nephroprotective aPC-PAR signaling in dNP.