Dynamics of cyclic GMP synthesis in retinal rods

被引:185
作者
Burns, ME [1 ]
Mendez, A
Chen, J
Baylor, DA
机构
[1] Stanford Univ, Med Ctr, Dept Neurobiol, Stanford, CA 94305 USA
[2] Univ So Calif, Keck Sch Med, Doheny Eye Inst, Mary D Allen Lab Vis Res, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sch Med, Dept Ophthalmol, Los Angeles, CA 90033 USA
[4] Univ So Calif, Keck Sch Med, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
[5] Univ Calif Davis, Dept Psychiat, Davis, CA 95616 USA
[6] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
关键词
D O I
10.1016/S0896-6273(02)00911-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In retinal rods, Ca2+ exerts negative feedback control on cGMP synthesis by guanylate cyclase (GC). This feedback loop was disrupted in mouse rods lacking guanylate cyclase activating proteins GCAP1 and GCAP2 (GCAPs(-/-)). Comparison of the behavior of wild-type and GCAPs(-/-) rods allowed us to investigate the role of the feedback loop in normal rod function. We have found that regulation of GC is apparently the only Ca2+ feedback loop operating during the single photon response. Analysis of the rods' light responses and cellular dark noise suggests that GC normally responds to light-driven changes in [Ca2+] rapidly and highly cooperatively. Rapid feedback to GC speeds the rod's temporal responsiveness and improves its signal-to-noise ratio by minimizing fluctuations in cGMP.
引用
收藏
页码:81 / 91
页数:11
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