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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.

DOI:10.1021/bi00355a044
PMID:3011071
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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