期刊
JOURNAL OF GENERAL PHYSIOLOGY
卷 123, 期 1, 页码 63-75出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1085/jgp.200308952
关键词
retina; phototransduction; ion channel; signal transduction; light adaptation
类别
资金
- NEI NIH HHS [R01 EY005498, R56 EY005498, EY-05498] Funding Source: Medline
- NATIONAL EYE INSTITUTE [R01EY005498] Funding Source: NIH RePORTER
In the mammalian retina, cone photoreceptors efficiently adapt to changing background light intensity and, therefore, are able to signal small differences in luminance between objects and backgrounds, even when the absolute intensity of the background changes over five to six orders of magnitude. Mammalian rod photoreceptors, in contrast, adapt very little and only at intensities that nearly saturate the amplitude of their photoresponse. In search of a molecular explanation for this observation we assessed Ca2+-dependent modulation of ligand sensitivity in cyclic GMP-gated (CNG) ion channels of intact mammalian rods and cones. Solitary photoreceptors were isolated by gentle proteolysis of ground squirrel retina. Rods and cones were distinguished by whether or not their outer segments bind PNA lectin. We measured membrane currents under voltage-clamp in photoreceptors loaded with Diazo-2, a caged Ca2+ chelator, and fixed concentrations of 8Br-cGMP. At 600 nM free cytoplasmic Ca2+ the midpoint of the cone CNG channels sensitivity to 8BrcGMP, K-8BrcGMP(1/2), is similar to2.3 muM. The ligand sensitivity is less in rod than in cone channels. Instantly decreasing cytoplasmic Ca2+ to < 30 nM activates a large inward membrane current in cones, but not in rods. Current activation arises from a Ca2+-dependent modulation of cone CNG channels, presumably because of an increase in their affinity to the cyclic nucleotide. The time course of current activation is temperature dependent; it is well described by a single exponential process of similar to480 ms time constant at 20-21degreesC and 138 ms at 32degreesC. The absence of detectable Ca2+-dependent CNG current modulation in intact rods, in view of the known channel modulation by calmodulin in-vitro, affirms the modulation in intact rods may only occur at low Ca2+ concentrations, those expected at intensities that nearly saturate the rod photoresponse. The correspondence between Ca2+ dependence of CNG modulation and the ability to light adapt suggest these events are correlated in photoreceptors.
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