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蝾螈视网膜视锥细胞中钠依赖的钙外排与敏感性调节

Sodium-dependent calcium extrusion and sensitivity regulation in retinal cones of the salamander.

作者信息

Nakatani K, Yau K W

机构信息

Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

J Physiol. 1989 Feb;409:525-48. doi: 10.1113/jphysiol.1989.sp017511.

DOI:10.1113/jphysiol.1989.sp017511
PMID:2479741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1190458/
Abstract
  1. Membrane current was recorded from an isolated, dark-adapted salamander cone by sucking its inner segment into a tight-fitting glass pipette containing Ringer solution. The outer segment of the cell was exposed to a bath solution that could be changed rapidly. 2. After removing Na+ from the bath Ringer solution for a short period of time in darkness (the 'loading period'), a transient inward current was observed upon restoring it in bright light. A similar but longer-lasting current was observed when Na+ was restored in the light after a large Ca2+ influx was induced through the light-sensitive conductance in darkness. 3. The above transient current was not observed if Li+ or guanidinium was substituted for Na+ in the light, or if Ba2+ was substituted for Ca2+ during the dark loading period. However, a current was observed if Sr2+ was the substituting ion for Ca2+ during loading. These observations suggested that the current was associated with an electrogenic Na+-dependent Ca2+ efflux at the cone outer segment. 4. The saturated amplitude of the exchange current was 12-25 pA with a mean around 16 pA. This is very comparable to that measured in the outer segment of a salamander rod under similar conditions. 5. By comparing a known Ca2+ load in a cone outer segment to the subsequent charge transfer through the exchange, we estimated that the stoichiometry of the exchange was near 3Na+:1Ca2+. 6. With a small Ca2+ load, or in the presence of Cs+ around the inner segment, the final temporal decline of the Na+-Ca2+ exchange current was roughly exponential, with a mean time constant of about 100 ms. This decline is about four times faster than that measured in rods. We interpret the shorter time constant in cones to reflect a faster rate of decline of intracellular free Ca2+ in their outer segments resulting from the exchange activity. 7. In the absence of external Na+, and hence any Na+-dependent Ca2+ efflux, the absolute sensitivity of a cone to a dim flash was several times higher than in normal Ringer solution. 8. A roughly similar increase in light sensitivity was observed for a rod under the same conditions. 9. We conclude that the Na+-dependent Ca2+ efflux, through lowering intracellular free Ca2+ in the light, has a role in regulating the absolute light sensitivity in cones as it does in rods.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 通过将一只暗适应的蝾螈视锥细胞的内段吸入装有林格液的紧密贴合的玻璃微管中,记录其膜电流。细胞的外段暴露于可快速更换的浴液中。2. 在黑暗中短时间从浴液林格液中去除Na⁺(“加载期”)后,在强光下恢复Na⁺时观察到短暂的内向电流。当在黑暗中通过光敏电导诱导大量Ca²⁺内流后在光照下恢复Na⁺时,观察到类似但持续时间更长的电流。3. 如果在光照下用Li⁺或胍盐替代Na⁺,或者在黑暗加载期用Ba²⁺替代Ca²⁺,则不会观察到上述短暂电流。然而,如果在加载期用Sr²⁺替代Ca²⁺作为替代离子,则会观察到电流。这些观察结果表明,该电流与视锥细胞外段的一种电致Na⁺依赖性Ca²⁺外流有关。4. 交换电流的饱和幅度为12 - 25 pA,平均约为16 pA。这与在类似条件下蝾螈视杆细胞外段测得的结果非常可比。5. 通过将视锥细胞外段中已知的Ca²⁺负载与随后通过交换的电荷转移进行比较,我们估计交换的化学计量比接近3Na⁺:1Ca²⁺。6. 对于小的Ca²⁺负载,或者在内段周围存在Cs⁺的情况下,Na⁺-Ca²⁺交换电流的最终时间衰减大致呈指数形式,平均时间常数约为100 ms。这种衰减比在视杆细胞中测得的快约四倍。我们将视锥细胞中较短的时间常数解释为反映其外段中由于交换活动导致的细胞内游离Ca²⁺下降速度更快。7. 在没有外部Na⁺,因此没有任何Na⁺依赖性Ca²⁺外流的情况下,视锥细胞对弱闪光的绝对敏感度比在正常林格液中高几倍。8. 在相同条件下对视杆细胞观察到大致类似的光敏感度增加。9. 我们得出结论,Na⁺依赖性Ca²⁺外流通过在光照下降低细胞内游离Ca²⁺,在调节视锥细胞的绝对光敏感度方面与在视杆细胞中一样起作用。(摘要截断于400字)

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