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Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina

机译:暂时性糖尿病诱发的小鼠视网膜不同层的生化变化

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摘要

To discover the mechanisms underlying the progression of diabetic retinopathy (DR), a more comprehensive understanding of the biomolecular processes in individual retinal cells subjected to hyperglycemia is required. Despite extensive studies, the changes in the biochemistry of retinal layers during the development of DR are not well known. In this study, we aimed to determine a more detailed understanding of the natural history of DR in Akita/+ (type 1 diabetes model) male mice with different duration of diabetes. Employing label-free spatially resolved Fourier transform infrared (FT-IR) chemical imaging engaged with multivariate analysis enabled us to identify temporal-dependent reproducible biomarkers of the individual retinal layers from mice with 6 weeks,12 weeks, 6 months, and 10 months of age. We report, for the first time, the nature of the biochemical alterations over time in the biochemistry of distinctive retinal layers namely photoreceptor retinal layer (PRL), inner nuclear layer (INL), and plexiform layers (OPL, IPL). Moreover, we present the molecular factors associated with the changes in the protein structure and cellular lipids of retinal layers induced by different duration of diabetes. Our paradigm provides a new conceptual framework for a better understanding of the temporal cellular changes underlying the progression of DR.
机译:为了发现糖尿病性视网膜病变(DR)进展的潜在机制,需要对经受高血糖的单个视网膜细胞中的生物分子过程有更全面的了解。尽管进行了广泛的研究,但DR发展过程中视网膜层生化的变化尚不清楚。在这项研究中,我们旨在确定对具有不同糖尿病持续时间的秋田/ +(1型糖尿病模型)雄性小鼠DR自然病史的更详细了解。使用无标签的空间分辨傅立叶变换红外(FT-IR)化学成像技术进行多变量分析,使我们能够识别6周,12周,6个月和10个月的小鼠视网膜个别视网膜层的时间依赖性可复制生物标记。年龄。我们首次报告了独特的视网膜层,即感光视网膜层(PRL),内核层(INL)和丛状层(OPL,IPL)的生化过程中生物化学变化随时间变化的性质。此外,我们介绍了与糖尿病持续时间不同引起的视网膜层蛋白质结构和细胞脂质变化相关的分子因素。我们的范例提供了一个新的概念框架,可以更好地理解DR进展背后的颞细胞变化。

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