Murata S, Matsumura Y, Takada K, Asai Y, Takaoka M, Morimoto S
Department of Pharmacology, Osaka University of Pharmaceutical Sciences, Japan.
J Pharmacol Exp Ther. 1995 Sep;274(3):1524-30.
We and other investigators obtained evidence that platelets stimulate endothelin-1 (ET-1) production at both message and protein levels in vascular endothelial cells (ECs), and that platelet-derived transforming growth factor-beta 1 (TGF-beta 1) is responsible for this stimulation. In the present study, we examined the effects of acidification or heat treatment, known to activate latent TGF-beta 1, on the platelet supernatant-induced ET-1 production in cultured porcine aortic ECs. Supernatant of platelets (6.0 x 10(8) platelets/ml) aggregated by adenosine diphosphate contained large amounts of TGF-beta 1, but were almost in a latent form, and the proportion of active TGF-beta 1 in the supernatant was increased markedly in the case of acidification or heat treatment. These treatments also significantly potentiated the supernatant-induced stimulation of prepro ET-1 mRNA expression and the ET-1 release in ECs. Purified TGF-beta 1 also enhanced ET-1 release, dose-dependently, but the enhancement declined at the higher concentrations. Thus, powerful stimulation of ET-1 production by platelet supernatant after acidification or heat treatment cannot be explained only by increments in active TGF-beta 1. The supernatant-induced stimulation of ET-1 synthesis was significantly inhibited by concomitant treatment of TGF-beta 1 neutralizing antibody, but this inhibition was incomplete even at a concentration that abolished TGF-beta 1-induced maximal stimulation. These results suggest that platelet-induced stimulation and subsequent acidification and heat treatment-induced potentiation on endothelial ET-1 production depend closely on release and activation of TGF-beta 1 derived from platelets.(ABSTRACT TRUNCATED AT 250 WORDS)
我们和其他研究人员获得的证据表明,血小板在血管内皮细胞(ECs)的信息和蛋白质水平上刺激内皮素-1(ET-1)的产生,并且血小板衍生的转化生长因子-β1(TGF-β1)是这种刺激的原因。在本研究中,我们研究了已知可激活潜伏TGF-β1的酸化或热处理对培养的猪主动脉ECs中血小板上清液诱导的ET-1产生的影响。由二磷酸腺苷聚集的血小板(6.0×10⁸个血小板/毫升)的上清液含有大量的TGF-β1,但几乎处于潜伏形式,在酸化或热处理的情况下,上清液中活性TGF-β1的比例显著增加。这些处理还显著增强了上清液诱导的ECs中前体ET-1 mRNA表达的刺激和ET-1的释放。纯化的TGF-β1也剂量依赖性地增强了ET-1的释放,但在较高浓度下这种增强作用下降。因此,酸化或热处理后血小板上清液对ET-1产生的强烈刺激不能仅用活性TGF-β1的增加来解释。TGF-β1中和抗体的联合处理显著抑制了上清液诱导的ET-1合成刺激,但即使在消除TGF-β1诱导的最大刺激的浓度下,这种抑制也是不完全的。这些结果表明,血小板诱导的刺激以及随后的酸化和热处理诱导的对内皮ET-1产生的增强作用密切依赖于血小板衍生的TGF-β1的释放和激活。(摘要截短至250字)