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首页> 外文期刊>Investigative ophthalmology & visual science >Photoreceptor Cells Influence Retinal Vascular Degeneration in Mouse Models of Retinal Degeneration and Diabetes
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Photoreceptor Cells Influence Retinal Vascular Degeneration in Mouse Models of Retinal Degeneration and Diabetes

机译:感光细胞影响视网膜变性和糖尿病小鼠模型中的视网膜血管变性。

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Purpose: Loss of photoreceptor cells is associated with retinal vascular degeneration in retinitis pigmentosa, whereas the presence of photoreceptor cells is implicated in vascular degeneration in diabetic retinopathy. To investigate how both the absence and presence of photoreceptors could damage the retinal vasculature, we compared two mouse models of photoreceptor degeneration (opsina??/a?? and RhoP23H/P23Ha??) and control C57Bl/5J mice, each with and without diabetes. Methods: Retinal thickness, superoxide, expression of inflammatory proteins, ERG and optokinetic responses, leukocyte cytotoxicity, and capillary degeneration were evaluated at 1 to 10 months of age using published methods. Results: Retinal photoreceptor cells degenerated completely in the opsin mutants by 2 to 4 months of age, and visual function subsided correspondingly. Retinal capillary degeneration was substantial while photoreceptors were still present, but slowed after the photoreceptors degenerated. Diabetes did not further exacerbate capillary degeneration in these models of photoreceptor degeneration, but did cause capillary degeneration in wild-type animals. Photoreceptor cells, however, did not degenerate in wild-type diabetic mice, presumably because the stress responses in these cells were less than in the opsin mutants. Retinal superoxide and leukocyte damage to retinal endothelium contributed to the degeneration of retinal capillaries in diabetes, and leukocyte-mediated damage was increased in both opsin mutants during photoreceptor cell degeneration. Conclusions: Photoreceptor cells affect the integrity of the retinal microvasculature. Deterioration of retinal capillaries in opsin mutants was appreciable while photoreceptor cells were present and stressed, but was less after photoreceptors degenerated. This finding proves relevant to diabetes, where persistent stress in photoreceptors likewise contributes to capillary degeneration.
机译:目的:光感受器细胞的丢失与色素性视网膜炎的视网膜血管变性有关,而糖尿病视网膜病变中的光感受器细胞的存在与血管变性有关。为了研究缺少和存在感光细胞如何损害视网膜脉管系统,我们比较了两种小鼠的感光细胞变性模型(opsinaΔα/αβ和RhoP23H /P23Haα)和对照C57Bl / 5J小鼠,分别有和没有糖尿病。方法:使用已发表的方法,在1至10个月大时评估视网膜厚度,超氧化物,炎症蛋白的表达,ERG和视动反应,白细胞的细胞毒性以及毛细血管变性。结果:视蛋白突变体中的视网膜感光细胞在2到4个月大时完全变性,并且视觉功能相应消退。视网膜毛细血管退行性变很明显,但仍存在感光器,但在感光器退化后减慢了速度。在这些光感受器变性模型中,糖尿病并未进一步加剧毛细血管变性,但在野生型动物中却引起毛细血管变性。然而,感光细胞在野生型糖尿病小鼠中并未退化,可能是因为这些细胞中的应激反应小于视蛋白突变体中的应激反应。糖尿病中视网膜过氧化物和白细胞对视网膜内皮的损伤是导致视网膜毛细血管变性的原因,在感光细胞变性期间,两种视蛋白突变体中白细胞介导的损伤均增加。结论:感光细胞影响视网膜微脉管系统的完整性。当存在和受压感光细胞时,视蛋白突变体中视网膜毛细血管的恶化是明显的,但是在感光细胞退化后,视网膜毛细血管的恶化程度较小。这一发现被证明与糖尿病有关,在糖尿病中,感光细胞的持续压力同样会导致毛细血管变性。

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