首页> 美国卫生研究院文献>The Journal of Neuroscience >Exchange of Cone for Rod Phosphodiesterase 6 Catalytic Subunits in Rod Photoreceptors Mimics in Part Features of Light Adaptation
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Exchange of Cone for Rod Phosphodiesterase 6 Catalytic Subunits in Rod Photoreceptors Mimics in Part Features of Light Adaptation

机译:杆的感光细胞模拟杆光磷酸二酯酶6催化亚基的锥体交换的部分光适应特征

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摘要

Despite the expression of homologous phototransduction components, the molecular basis for differences in light-evoked responses between rod and cone photoreceptors remains unclear. We examined the role of cGMP phosphodiesterase (PDE6) in this difference by expressing cone PDE6 (PDE6C) in rd1/rd1 rods lacking rod PDE6 (PDE6AB) using transgenic mice. The expression of PDE6C rescues retinal degeneration observed in rd1/rd1 rods. Double-transgenic rods (PDE6C++) were compared with rd1/+ rods based on similar PDE6 expression. PDE6C increased the basal PDE activity and speeded the rate-limiting step for phototransduction deactivation, causing rod photoresponses to appear light adapted, with reduced dark current and sensitivity and faster response kinetics. When PDE6C++ and rd1/+ rods were exposed to similar background light, rd1/+ rods displayed greater desensitization. These results indicate an increased spontaneous activity and faster deactivation of PDE6C compared with PDE6AB in darkness, but that background light increases steady PDE6C activity to a lesser extent. In addition to accelerating the recovery of the photoresponse, faster PDE6C deactivation may blunt the rise in background-induced steady PDE6C activity. Therefore, higher basal PDE6C activity and faster deactivation together partially account for faster and less sensitive cone photoresponses in darkness, whereas a reduced rise of steady PDE6C activity in background light may allow cones to avoid saturation.>Significance Statement Cones are the primary photoreceptors responsible for most of our visual experience. Cone light responses are less sensitive and display speeded responses compared with rods. Despite the fact that rods and cones use a G-protein signaling cascade with similar organization, the mechanistic basis for these differences remains unclear. Here, we examined the role of distinct isoforms of PDE6, the effector enzyme in phototransduction, in these differences. We developed a transgenic mouse model that expresses cone PDE6 in rods and show that the cone PDE6 isoform is partially responsible for the difference in sensitivity and response kinetics between rods and cones.
机译:尽管表达了同源的光转导成分,但杆状和锥状感光体之间的光诱发反应差异的分子基础仍然不清楚。我们通过使用转基因小鼠在缺少杆PDE6(PDE6AB)的rd1 / rd1杆中表达锥PDE6(PDE6C),研究了cGMP磷酸二酯酶(PDE6)在这种差异中的作用。 PDE6C的表达可挽救在rd1 / rd1棒中观察到的视网膜变性。基于相似的PDE6表达,将双转基因棒(PDE6C ++)与rd1 / +棒进行了比较。 PDE6C增加了基础PDE活性,并加快了光转导失活的限速步骤,使杆的光响应表现出适应光的特性,从而降低了暗电流和灵敏度,并加快了响应动力学。当PDE6C ++和rd1 / +杆暴露于相似的背景光时,rd1 / +杆显示出更大的脱敏性。这些结果表明,与黑暗中的PDE6AB相比,PDE6C的自发活性增加,灭活速度更快,但是背景光在较小程度上增加了稳定的PDE6C活性。除了加速光响应的恢复外,更快的PDE6C失活可能会抑制背景诱导的稳定PDE6C活性的上升。因此,较高的基础PDE6C活性和更快的失活​​共同部分地解释了黑暗中视锥细胞的更快和更不敏感的光响应,而降低的稳定PDE6C活性在背景光下的升高可能会使视锥细胞避免饱和。>重要性声明是负责我们大部分视觉体验的主要感光器。与棒相比,锥光响应较不敏感并且显示出更快的响应。尽管杆和锥使用具有相似组织的G蛋白信号级联的事实,但这些差异的机制基础仍不清楚。在这里,我们检查了PDE6的不同同工型(在光转导中的效应酶)在这些差异中的作用。我们开发了一种在杆中表达视锥细胞PDE6的转基因小鼠模型,并表明视锥细胞PDE6同工型部分负责视杆和视锥细胞之间的敏感性和响应动力学差异。

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