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3',5'-环磷酸鸟苷刺激牛视网膜视杆外段纯化盘膜中主动积累的钙的释放。

Guanosine 3',5'-cyclic monophosphate stimulates release of actively accumulated calcium in purified disks from rod outer segments of bovine retina.

作者信息

Puckett K L, Goldin S M

出版信息

Biochemistry. 1986 Apr 8;25(7):1739-46. doi: 10.1021/bi00355a044.

Abstract

Parallel lines of evidence have suggested that light initiates changes in both cGMP metabolism and calcium levels in rod outer segments (ROS). We report that cGMP stimulates release of a pool of Ca2+ actively accumulated within purified ROS disks. Disks were purified and actively loaded with 45Ca2+ by an associated ATP-dependent calcium uptake activity as previously described [Puckett, K.L., Aronson, E.T., & Goldin, S.M. (1985) Biochemistry 24, 390-400]. Spikes of 45Ca2+ released from disks were observed in a rapid superfusion system. The Ca2+ release was specifically stimulated by physiological levels of cGMP (Kapp approximately 20 microM; Hill coefficient = 1.7). 8-Bromo-cGMP could also activate the release mechanism, but cAMP was ineffective. At cGMP levels of greater than or equal to 100 microM, approximately 20% of the loaded Ca2+ was released. The Ca2+ release rate at saturating cGMP levels reached a maximum within the 10-s time resolution of the assay system. In contrast to other recent reports of cGMP activation of ROS ion conductances, the majority of the release activity terminated in a spontaneous manner, suggestive of an intrinsic inactivation process. The amount of Ca2+ released and the release kinetics were similar to the presence or absence of an unbleached pool of rhodopsin. Cyclic nucleotides did not stimulate release from disks passively equilibrated with 45Ca2+, i.e., in the absence of ATP but otherwise under identical conditions. Preincubation of the disks with cGMP also reduced the level of ATP-dependent Ca2+ uptake (approximately 30%); this apparent inhibition may be due to activation of the release mechanism, rather than direct modulation of the uptake activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

多条平行的证据表明,光可引发视杆细胞外段(ROS)中cGMP代谢和钙水平的变化。我们报告称,cGMP可刺激纯化的ROS盘片中主动积累的一部分Ca2+释放。如先前所述[Puckett, K.L., Aronson, E.T., & Goldin, S.M. (1985) Biochemistry 24, 390 - 400],通过相关的ATP依赖型钙摄取活性对盘片进行纯化并主动加载45Ca2+。在快速灌流系统中观察到从盘片中释放出的45Ca2+尖峰。cGMP的生理水平可特异性刺激Ca2+释放(Kapp约为20 microM;希尔系数 = 1.7)。8-溴-cGMP也可激活释放机制,但cAMP无效。当cGMP水平大于或等于100 microM时,约20%加载的Ca2+被释放。在检测系统10秒的时间分辨率内,饱和cGMP水平下的Ca2+释放速率达到最大值。与最近关于cGMP激活ROS离子电导的其他报道不同,大多数释放活性以自发方式终止,提示存在内在失活过程。释放的Ca2+量和释放动力学与有无未漂白的视紫红质池相似。环核苷酸不会刺激与45Ca2+被动平衡的盘片释放Ca2+,即在无ATP但其他条件相同的情况下。用cGMP预孵育盘片也会降低ATP依赖型Ca2+摄取水平(约30%);这种明显的抑制可能是由于释放机制的激活,而非对摄取活性的直接调节。(摘要截短于250字)

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