Sun Wentian, Khoo Hoon Eng, Tan Chee Hong
Department of Biochemistry, Faculty of Medicine, National University of Singapore, 10 Kent Ridge Crescent, Singapore, 119260, Republic of Singapore.
J Biochem Mol Biol. 2005 May 31;38(3):314-9. doi: 10.5483/bmbrep.2005.38.3.314.
Adenosine, as a ubiquitous metabolite, mediates many physiological functions via activation of plasma membrane receptors. Mechanisms of most of its physiological roles have been studied extensively, but research on adenosine-induced apoptosis (AIA) has only started recently. In this study we demonstrate that adenosine dose-dependently triggered apoptosis of cultured baby hamster kidney (BHK) cells. Adenosine-induced apoptotic cell death was characterized by DNA laddering, changes in nuclear chromatin morphology and phosphatidylserine staining. Apoptosis was also quantified by flow cytometry. Results suggest the involvement of adenosine A1 and A3 receptors as well as equilibrative nucleoside transporters in apoptosis induced by adenosine. These results indicate a receptor-transporter co-signaling mechanism in AIA in BHK cells. The involvement of A1 and A3 receptors also implies a possible apoptotic pathway mediated by G protein-coupled receptors.
腺苷作为一种普遍存在的代谢产物,通过激活质膜受体介导多种生理功能。其大多数生理作用的机制已得到广泛研究,但对腺苷诱导的细胞凋亡(AIA)的研究直到最近才开始。在本研究中,我们证明腺苷能剂量依赖性地触发培养的幼仓鼠肾(BHK)细胞凋亡。腺苷诱导的凋亡性细胞死亡表现为DNA梯状条带、核染色质形态变化和磷脂酰丝氨酸染色。凋亡也通过流式细胞术进行定量分析。结果表明腺苷A1和A3受体以及平衡核苷转运体参与了腺苷诱导的细胞凋亡。这些结果表明在BHK细胞的AIA中存在受体-转运体共信号机制。A1和A3受体的参与也意味着可能存在一条由G蛋白偶联受体介导的凋亡途径。