Matsumura Y, Takada K, Murakami A, Takaoka M, Morimoto S
Department of Pharmacology, Osaka University of Pharmaceutical Sciences, Japan.
Life Sci. 1996;58(13):1067-74. doi: 10.1016/0024-3205(96)00060-4.
Incubation of cultured porcine aortic endothelial cells (ECs) with plasmin resulted in a significant and concentration-dependent increase in endothelin-1 (ET-1) release from the cells. This increasing effect was completely inhibited by aprotinin but not by tranexamic acid, thereby suggesting that the plasmin-induced stimulation of ET-1 release requires the catalytic site but not the lysine binding site, in plasmin molecule. Plasmin stimulated the expression of prepro ET-1 mRNA in ECs. Actinomycin D chase experiments suggested that enhanced stability of ET-T mRNA could not account for the above plasmin-induced stimulation. It is likely that plasmin potentiates the endothelial ET-1 production, probably by the stimulation of ET-1 gene transcription. It remains to be seen whether the endothelial ET-1 production is enhanced after the thrombolytic therapy.
用纤溶酶孵育培养的猪主动脉内皮细胞(ECs),导致细胞释放内皮素-1(ET-1)显著增加,且呈浓度依赖性。这种增加效应被抑肽酶完全抑制,但氨甲环酸未起抑制作用,由此表明纤溶酶诱导的ET-1释放刺激需要纤溶酶分子中的催化位点而非赖氨酸结合位点。纤溶酶刺激了ECs中前内皮素原-1 mRNA的表达。放线菌素D追踪实验表明,ET-1 mRNA稳定性增强并不能解释上述纤溶酶诱导的刺激作用。纤溶酶可能通过刺激ET-1基因转录来增强内皮细胞ET-1的产生。溶栓治疗后内皮细胞ET-1的产生是否增强还有待观察。