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Single photon responses in Drosophila photoreceptors and their regulation by Ca2+

机译:果蝇感光细胞中的单光子响应及其受Ca2 +调控

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摘要

class="enumerated" style="list-style-type:decimal">Discrete events (quantum bumps) elicited by dim light were analysed in whole-cell voltage clamp of photoreceptors from dissociated Drosophila ommatidia. Bumps were automatically detected and analysed for amplitude, rise and decay times, and latency.The bump interval and amplitude distributions, and the ‘frequency of seeing’ curve conformed to Poisson predictions for the absorption of single photons.At resting potential (−70 mV), bumps averaged 10 pA in peak amplitude with a half-width of ca 20 ms, representing simultaneous activation of ca 15 channels.The macroscopic response to flashes containing up to at least 750 photons were predicted by the linear summation of quantum bumps convolved with their latency dispersion.Bump duration was unaffected by lowering the extracellular Ca2+ concentration ([Ca2+]o) from 1.5 to 0.5 mM, but increased >10-fold between 0.5 mM Ca2+ and 0 Ca2+. Bump amplitude was constant over the range 1.5–100 μM, but decreased ca 5- to 10-fold at lower Ca2+ concentrations. Bump latency increased by ca 50 % between 1.5 mM and 100 μM Cao2+ but returned to near control levels in Ca2+-free solutions.At intermediate [Ca2+]o bumps were biphasic with a slow rising phase followed by rapid amplification and inactivation. This behaviour was mimicked in high [Ca2+]o by internal buffering with BAPTA, but not EGTA. This suggests that Ca2+ influx through the light-sensitive channels must first raise cytosolic Ca2+ to a threshold level before initiating a cycle of positive and negative feedback mediated by molecular targets within the same microvillus.Quantum bumps in trp mutants lacking the major class of light-sensitive channel were reduced in size (mean 3.5 pA) representing simultaneous activation of only one or two channels; however, a second rarer (10 %) class of large bump had an amplitude similar to wild-type (WT) bumps. Bumps in trpl mutants lacking the second class of light-sensitive channel were very similar to WT bumps, but with slightly slower decay times.In InaDP215 mutants, in which the association of the TRP channels with the INAD scaffolding molecule is disrupted, bumps showed a defect in quantum bump termination, but their amplitudes and latencies were near normal.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在解离的果蝇的光感受器的全细胞电压钳中分析了昏暗的光引起的离散事件(量子颠簸)。自动检测碰撞并分析其振幅,上升和衰减时间以及潜伏期。 碰撞间隔和振幅分布以及“可见频率”曲线符合对单光子吸收的Poisson预测。 在静止电位(-70 mV)时,颠簸平均峰值幅度为10 pA,半峰宽约为20 ms,表示同时激活了约15个通道。 宏观量子凸点与其潜伏时间色散卷积的线性总和预测了对包含至少750个光子的闪光的响应。 降低细胞外Ca 2 + 不会影响碰撞持续时间浓度([Ca 2 + ] o)从1.5至0.5 mM,但在0.5 mM Ca 2 + 和0 Ca 2+ <之间增加了10倍以上/ sup>。凸点幅度在1.5-100μM范围内是恒定的,但是在较低的Ca 2 + 浓度下降低了5到10倍。在1.5 mM和100μMCao 2 + 之间,碰撞延迟增加了约50%,但在无Ca 2 + 的溶液中恢复到接近控制水平。
  • 在中间[Ca 2 + ] o凸起是双相的,具有缓慢的上升阶段,随后迅速扩增并失活。通过使用BAPTA(而不是EGTA)进行内部缓冲,可以在高[Ca 2 + ] o中模仿此行为。这表明通过光敏通道流入的Ca 2 + 必须首先将胞浆Ca 2 + 升高至阈值水平,然后才能启动由分子介导的正反馈和负反馈循环 缺少主要光敏通道类别的trp突变体中的量子点减小了大小(平均3.5 pA),表示仅激活一个或两个通道。然而,第二类(10%)稀有大凸块的振幅类似于野生型(WT)凸块。缺少第二类光敏通道的trpl突变体中的凸起与WT凸起非常相似,但衰减时间稍慢。 在InaD P215 突变体中,具有INAD支架分子的TRP通道被破坏,凸起显示出量子凸起终止的缺陷,但其幅度和潜伏期接近正常。
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