Inserm, U626, Université de Méditerranée, Faculté de Médecine, 27 Boulevard Jean Moulin, 13385 Marseilles Cedex 5, France.
J Cell Sci. 2011 Apr 15;124(Pt 8):1224-30. doi: 10.1242/jcs.079889. Epub 2011 Mar 15.
Proprotein convertases (PCs) are a family of serine proteases that are involved in the post-translational processing and activation of a wide range of regulatory proteins. The upstream role of PCs in the control of many physiological and pathological processes generates a growing interest in understanding their regulation. Here, we demonstrate that the serine protease inhibitor plasminogen activator inhibitor 1 (PAI-1) forms an SDS-stable complex with the PC furin, which leads to the inhibition of the intra-Golgi activity of furin. It is known that elevated PAI-1 plasma levels are correlated with the occurrence of the metabolic syndrome and type 2 diabetes, and we show that PAI-1 reduces the furin-dependent maturation and activity of the insulin receptor and ADAM17: two proteins involved in the onset of these metabolic disorders. In addition to demonstrating that PAI-1 is an intracellular inhibitor of furin, this study also provides arguments in favor of an active role for PAI-1 in the development of metabolic disorders.
蛋白转化酶(PCs)是一类丝氨酸蛋白酶,参与广泛的调节蛋白的翻译后加工和激活。PCs 在许多生理和病理过程中的上游作用激发了人们对其调控机制的深入研究。本研究证实,丝氨酸蛋白酶抑制剂纤溶酶原激活物抑制剂 1(PAI-1)与 PC 弗林(furin)形成 SDS 稳定复合物,从而抑制弗林在高尔基体内的活性。已知血浆中 PAI-1 水平升高与代谢综合征和 2 型糖尿病的发生有关,我们发现 PAI-1 降低了胰岛素受体和 ADAM17 的成熟和活性,这两种蛋白参与了这些代谢紊乱的发生。本研究不仅证明了 PAI-1 是弗林的细胞内抑制剂,还为 PAI-1 在代谢紊乱发展中的积极作用提供了依据。