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肽稳态在代谢性视网膜退行性疾病中的相关性:转基因小鼠的治疗潜力

Relevance of Peptide Homeostasis in Metabolic Retinal Degenerative Disorders: Curative Potential in Genetically Modified Mice.

作者信息

Pöstyéni Etelka, Ganczer Alma, Kovács-Valasek Andrea, Gabriel Robert

机构信息

Department of Experimental Zoology and Neurobiology, University of Pécs, Pécs, Hungary.

János Szentágothai Research Centre, University of Pécs, Pécs, Hungary.

出版信息

Front Pharmacol. 2022 Jan 13;12:808315. doi: 10.3389/fphar.2021.808315. eCollection 2021.

Abstract

The mammalian retina contains approximately 30 neuropeptides that are synthetized by different neuronal cell populations, glia, and the pigmented epithelium. The presence of these neuropeptides leaves a mark on normal retinal molecular processes and physiology, and they are also crucial in fighting various pathologies (e.g., diabetic retinopathy, ischemia, age-related pathologies, glaucoma) because of their protective abilities. Retinal pathologies of different origin (metabolic, genetic) are extensively investigated by genetically manipulated mouse models that help us gain a better understanding of the molecular background of these pathomechanisms. These models offer opportunities to manipulate gene expression in different cell types to help reveal their roles in the preservation of retinal health or identify malfunction during diseases. In order to assess the current status of transgenic technologies available, we have conducted a literature survey focused on retinal disorders of metabolic origin, zooming in on the role of retinal neuropeptides in diabetic retinopathy and ischemia. First, we identified those neuropeptides that are most relevant to retinal pathologies in humans and the two clinically most relevant models, mice and rats. Then we continued our analysis with metabolic disorders, examining neuropeptide-related pathways leading to systemic or cellular damage and rescue. Last but not least, we reviewed the available literature on genetically modified mouse strains to understand how the manipulation of a single element of any given pathway (e.g., signal molecules, receptors, intracellular signaling pathways) could lead either to the worsening of disease conditions or, more frequently, to substantial improvements in retinal health. Most attention was given to studies which reported successful intervention against specific disorders. For these experiments, a detailed evaluation will be given and the possible role of converging intracellular pathways will be discussed. Using these converging intracellular pathways, curative effects of peptides could potentially be utilized in fighting metabolic retinal disorders.

摘要

哺乳动物的视网膜含有大约30种神经肽,这些神经肽由不同的神经元细胞群、神经胶质细胞和色素上皮细胞合成。这些神经肽的存在对正常视网膜分子过程和生理机能产生影响,并且由于它们的保护能力,在对抗各种病理状况(如糖尿病性视网膜病变、局部缺血、年龄相关性病变、青光眼)方面也至关重要。通过基因操作的小鼠模型对不同起源(代谢性、遗传性)的视网膜病变进行了广泛研究,这些模型有助于我们更好地理解这些病理机制的分子背景。这些模型提供了在不同细胞类型中操纵基因表达的机会,以帮助揭示它们在维持视网膜健康中的作用或识别疾病期间的功能异常。为了评估现有转基因技术的现状,我们进行了一项文献调查,重点关注代谢性起源的视网膜疾病,深入研究视网膜神经肽在糖尿病性视网膜病变和局部缺血中的作用。首先,我们确定了那些与人类以及两种临床上最相关的模型(小鼠和大鼠)的视网膜病变最相关的神经肽。然后我们继续对代谢紊乱进行分析,研究导致全身或细胞损伤及修复的神经肽相关途径。最后但同样重要的是,我们回顾了关于基因改造小鼠品系的现有文献,以了解对任何给定途径的单个元素(如信号分子、受体、细胞内信号通路)进行操纵如何可能导致疾病状况恶化,或者更常见的是,如何显著改善视网膜健康。我们最关注那些报道了针对特定疾病成功干预的研究。对于这些实验,将进行详细评估并讨论汇聚细胞内途径的可能作用。利用这些汇聚细胞内途径,肽的治疗效果可能被用于对抗代谢性视网膜疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97c/8793341/5cc55fed56ab/fphar-12-808315-g001.jpg

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