Appell K C, Barefoot D S
Department of Molecular Biology, A. H. Robins Research Laboratories, Richmond, VA 23220.
Biochem J. 1989 Oct 1;263(1):11-8. doi: 10.1042/bj2630011.
The effect of bradykinin on intracellular free Ca2+ and neurotransmitter secretion was investigated in the rat pheochromocytoma cell line PC12. Bradykinin was shown to induce a rapid, but transient, increase in intracellular free Ca2+ which could be separated into an intracellular Ca2+ release component and an extracellular Ca2+ influx component. The bradykinin-induced stimulation of intracellular free Ca2+ displayed a similar time course, concentration dependencies and extracellular Ca2+ dependence as that found for neurotransmitter release, indicating an association between intracellular free Ca2+ levels and neurotransmitter secretion. The selective BK1-receptor antagonist des-Arg9,[Leu8]BK (where BK is bradykinin) did not significantly affect the stimulation of intracellular free Ca2+ or neurotransmitter release. In contrast, these effects of bradykinin were effectively blocked by the selective BK2-receptor antagonist [Thi5,8,D-Phe7]BK, and mimicked by the BK2 partial agonist [D-Phe7]BK in a concentration-dependent manner. The stimulation of intracellular free Ca2+ and neurotransmitter release induced by bradykinin was shown not to involve voltage-sensitive Ca2+ channels, since calcium antagonists had no effect on either response at concentrations which effectively inhibit depolarization-induced responses. These results indicate that bradykinin, acting through the interaction with the BK2 receptor, stimulates an increase in intracellular free Ca2+ leading to neurotransmitter secretion. Furthermore, bradykinin-induced responses involve the release of intracellular Ca2+ and the influx of extracellular Ca2+ that is not associated with the activation of voltage-sensitive Ca2+ channels.
在大鼠嗜铬细胞瘤细胞系PC12中研究了缓激肽对细胞内游离Ca2+和神经递质分泌的影响。结果表明,缓激肽可诱导细胞内游离Ca2+迅速但短暂地增加,这一增加可分为细胞内Ca2+释放成分和细胞外Ca2+内流成分。缓激肽诱导的细胞内游离Ca2+刺激表现出与神经递质释放相似的时间进程、浓度依赖性和细胞外Ca2+依赖性,表明细胞内游离Ca2+水平与神经递质分泌之间存在关联。选择性BK1受体拮抗剂去-Arg9,[Leu8]BK(其中BK为缓激肽)对细胞内游离Ca2+的刺激或神经递质释放无显著影响。相反,缓激肽的这些作用被选择性BK2受体拮抗剂[Thi5,8,D-Phe7]BK有效阻断,并被BK2部分激动剂[D-Phe7]BK以浓度依赖的方式模拟。缓激肽诱导的细胞内游离Ca2+和神经递质释放的刺激不涉及电压敏感性Ca2+通道,因为钙拮抗剂在有效抑制去极化诱导反应的浓度下对两种反应均无影响。这些结果表明,缓激肽通过与BK2受体相互作用,刺激细胞内游离Ca2+增加,导致神经递质分泌。此外,缓激肽诱导的反应涉及细胞内Ca2+的释放和细胞外Ca2+的内流,这与电压敏感性Ca2+通道的激活无关。