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蛋白质组学分析与动物模型在视神经损伤疾病中的应用

Application of Proteomics Analysis and Animal Models in Optic Nerve Injury Diseases.

作者信息

Meng Zhaoyang, You Ran, Mahmood Arif, Yan Fancheng, Wang Yanling

机构信息

Department of Ophthalmology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.

Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.

出版信息

Brain Sci. 2023 Feb 26;13(3):404. doi: 10.3390/brainsci13030404.

Abstract

Optic nerve damage is a common cause of blindness. Optic nerve injury is often accompanied by fundus vascular disease, retinal ganglion cell apoptosis, and changes in retinal thickness. These changes can cause alterations in protein expression within neurons in the retina. Proteomics analysis offers conclusive evidence to decode a biological system. Furthermore, animal models of optic nerve injury made it possible to gain insight into pathological mechanisms, therapeutic targets, and effective treatment of such injuries. Proteomics takes the proteome as the research object and studies protein changes in cells and tissues. At present, a variety of proteomic analysis methods have been widely used in the research of optic nerve injury diseases. This review summarizes the application of proteomic research in optic nerve injury diseases and animal models of optic nerve injury. Additionally, differentially expressed proteins are summarized and analyzed. Various optic nerve injuries, including those associated with different etiologies, are discussed along with their potential therapeutic targets and future directions.

摘要

视神经损伤是失明的常见原因。视神经损伤常伴有眼底血管疾病、视网膜神经节细胞凋亡和视网膜厚度变化。这些变化可导致视网膜神经元内蛋白质表达的改变。蛋白质组学分析为解码生物系统提供了确凿证据。此外,视神经损伤动物模型使深入了解此类损伤的病理机制、治疗靶点和有效治疗成为可能。蛋白质组学以蛋白质组为研究对象,研究细胞和组织中的蛋白质变化。目前,多种蛋白质组学分析方法已广泛应用于视神经损伤疾病的研究。本文综述了蛋白质组学研究在视神经损伤疾病及视神经损伤动物模型中的应用。此外,还对差异表达蛋白进行了总结和分析。讨论了各种视神经损伤,包括与不同病因相关的损伤,以及它们潜在的治疗靶点和未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df30/10046207/961071949f91/brainsci-13-00404-g001.jpg

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