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野生型和Abca4基因敲除小鼠的视杆光感受器漂白后全反式视黄醛水平及脂褐素前体的形成。

All-trans retinal levels and formation of lipofuscin precursors after bleaching in rod photoreceptors from wild type and Abca4 mice.

作者信息

Adler Leopold, Chen Chunhe, Koutalos Yiannis

机构信息

Department of Ophthalmology, Medical University of South Carolina, Charleston, SC, United States.

Department of Ophthalmology, Medical University of South Carolina, Charleston, SC, United States.

出版信息

Exp Eye Res. 2017 Feb;155:121-127. doi: 10.1016/j.exer.2017.02.007. Epub 2017 Feb 17.

Abstract

The accumulation of lipofuscin in the cells of the retinal pigment epithelium (RPE) is thought to play an important role in the development and progression of degenerative diseases of the retina. The bulk of RPE lipofuscin originates in reactions of the rhodopsin chromophore, retinal, with components of the photoreceptor outer segment. The 11-cis retinal isomer is generated in the RPE and supplied to rod photoreceptor outer segments where it is incorporated as the chromophore of rhodopsin. It is photoisomerized during light detection to all-trans and subsequently released by photoactivated rhodopsin as all-trans retinal, which is removed through reduction to all-trans retinol in a reaction requiring metabolic input in the form of NADPH. Both 11-cis and all-trans retinal can form lipofuscin precursor fluorophores in rod photoreceptor outer segments. Increased accumulation of lipofuscin has been suggested to result from excess formation of lipofuscin precursors due to buildup of all-trans retinal released by light exposure. In connection with this suggestion, the Abca4 transporter protein, an outer segment protein defects in which result in recessive Stargardt disease, has been proposed to promote the removal of all-trans retinal by facilitating its availability for reduction. To examine this possibility, we have measured the outer segment levels of all-trans retinal, all-trans retinol, and of lipofuscin precursors after bleaching by imaging the fluorescence of single rod photoreceptors isolated from wild type and Abca4 mice. We found that all-trans retinol and all-trans retinal levels increased after bleaching in both wild type and Abca4 rods. At all times after bleaching, there was no significant difference in all-trans retinal levels between the two strains. All-trans retinol levels were not significantly different between the two strains at early times, but were lower in Abca4 rods at times longer than 20 min after bleaching. Bleaching in the presence of lower metabolic substrate concentrations resulted in higher all-trans retinal levels and increased formation of lipofuscin precursors in both wild type and Abca4 rods. The results show that conditions that result in buildup of all-trans retinal levels result in increased generation of lipofuscin precursors in both wild type and Abca4 rods. The results are consistent with the proposal that Abca4 facilitates the reduction of all-trans retinal to retinol; absence of Abca4 however does not appear to be associated with higher all-trans retinal levels compared to wild type.

摘要

视网膜色素上皮(RPE)细胞中脂褐素的积累被认为在视网膜退行性疾病的发生和发展中起重要作用。大部分RPE脂褐素起源于视紫红质发色团视网膜与光感受器外段成分的反应。11-顺式视网膜异构体在RPE中生成,并供应给视杆光感受器外段,在那里它作为视紫红质的发色团被整合。在光检测过程中,它被光异构化为全反式,随后由光激活的视紫红质以全反式视网膜的形式释放,通过在需要以NADPH形式提供代谢输入的反应中还原为全反式视黄醇而被清除。11-顺式和全反式视网膜都可以在视杆光感受器外段形成脂褐素前体荧光团。有人提出,脂褐素积累增加是由于光暴露释放的全反式视网膜积累导致脂褐素前体形成过多。与此建议相关,Abca4转运蛋白是一种外段蛋白,其缺陷会导致隐性Stargardt病,有人提出它通过促进全反式视网膜的还原可用性来促进其清除。为了检验这种可能性,我们通过对从野生型和Abca4小鼠分离的单个视杆光感受器的荧光成像,测量了漂白后全反式视网膜、全反式视黄醇和脂褐素前体的外段水平。我们发现,在野生型和Abca4视杆中,漂白后全反式视黄醇和全反式视网膜水平均升高。在漂白后的所有时间里,两种品系的全反式视网膜水平均无显著差异。在早期,两种品系的全反式视黄醇水平无显著差异,但在漂白后20分钟以上的时间里,Abca4视杆中的全反式视黄醇水平较低。在较低代谢底物浓度下进行漂白会导致野生型和Abca4视杆中的全反式视网膜水平升高,并增加脂褐素前体的形成。结果表明,导致全反式视网膜水平积累的条件会导致野生型和Abca4视杆中脂褐素前体的生成增加。这些结果与Abca4促进全反式视网膜还原为视黄醇的提议一致;然而,与野生型相比,Abca4的缺失似乎与更高的全反式视网膜水平无关。

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