首页> 美国卫生研究院文献>The Journal of Neuroscience >Constitutive Light Adaptation in Rods from G90D Rhodopsin: A Mechanism for Human Congenital Nightblindness without Rod Cell Loss
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Constitutive Light Adaptation in Rods from G90D Rhodopsin: A Mechanism for Human Congenital Nightblindness without Rod Cell Loss

机译:G90D视紫红质棒中的本构光适应:人类先天性夜盲的一种机制无棒细胞损失

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摘要

A dominant form of human congenital nightblindness is caused by a gly90→asp (G90D) mutation in rhodopsin. G90D has been shown to activate the phototransduction cascade in the absence of lightin vitro. Such constitutive activity of G90D rhodopsinin vivo would desensitize rod photoreceptors and lead to nightblindness. In contrast, other rhodopsin mutations typically give rise to nightblindness by causing rod cell death. Thus, the proposed desensitization without rod degeneration would be a novel mechanism for this disorder. To explore this possibility, we induced mice to express G90D opsin in their rods and then examined rod function and morphology, after first crossing the transgenic animals with rhodopsin knock-out mice to obtain appropriate levels of opsin expression. The G90D mouse opsin bound the chromophore and formed a bleachable visual pigment with λmax of 492 nm that supported rod photoresponses. (G+/−, R+/−) retinas, heterozygous for both G90D and wild-type (WT) rhodopsin, possessed normal numbers of photoreceptors and had a normal rhodopsin complement but exhibited considerable loss of rod sensitivity as measured electroretinographically. The rod photoresponses were desensitized, and the response time to peak was faster than in (R+/−) animals. An equivalent desensitization resulted by exposing WT retinas to a background light producing 82 photoisomerizations rod−1sec−1, suggesting that G90D rods in darkness act as if they are partially “light-adapted.” Adding a second G90D allele gave (G+/+, R+/−) animals that exhibited a further increase of equivalent background light level but had no rod cell loss by 24 weeks of age. (G+/+, R−/−) retinas that express only the mutant rhodopsin develop normal rod outer segments and show minimal rod cell loss even at 1 year of age. We conclude that G90D is constitutively active in mouse rods in vivo but that it does not cause significant rod degeneration. Instead, G90D desensitizes rods by a process equivalent to light adaptation.
机译:人类先天性夜盲的一种主要形式是由视紫红质中的gly90→asp(G90D)突变引起的。 G90D已显示在不存在体外光的情况下可以激活光转导级联反应。 G90D视紫红质在体内的这种组成活性将使杆感光细胞脱敏并导致夜盲症。相反,其他视紫红质突变通常通过引起杆状细胞死亡而引起夜盲症。因此,所提出的无杆变性的脱敏将是这种疾病的新机制。为了探索这种可能性,我们首先将转基因动物与视紫红质剔除小鼠杂交以获得合适水平的视蛋白表达,然后诱导小鼠在其视杆中表达G90D视蛋白,然后检查视杆功能和形态。 G90D小鼠视蛋白与发色团结合,形成λmax为492 nm的可漂白可视颜料,支持杆的光响应。 G90D和野生型(WT)视紫红质均是杂合的(G +/-,R +/-)视网膜具有正常数量的感光细胞和正常的视紫红质补体,但如视网膜电图所测,其杆敏感性显着降低。杆的光响应被脱敏,并且峰响应时间比(R +/-)动物快。将WT视网膜暴露于背景光下会产生等价的脱敏,产生82个光异构化棒 -1 sec -1 ,这表明G90D棒在黑暗中的行为就好像它们是部分“光” -适应。”添加第二个G90D等位基因使(G + / +,R ++ /-)动物表现出等效背景光水平的进一步提高,但到24周龄时却没有杆状细胞损失。仅表达突变型视紫红质的(G + / +,R-/-)视网膜发育正常的杆外段,即使在1岁时也显示出最小的杆细胞损失。我们得出结论,G90D在体内小鼠杆中具有组成性活性,但它不会引起杆的明显变性。取而代之的是,G90D通过等效于光适应的过程对杆进行脱敏。

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