神经系统疾病中的过氧化物酶体和pexophagy

IF 6.2 3区 综合性期刊 Q1 Multidisciplinary Fundamental Research Pub Date : 2024-11-01 DOI:10.1016/j.fmre.2023.04.016
Weilin Xu , Jun Yan , Anwen Shao , Cameron Lenahan , Liansheng Gao , Haijian Wu , Jingwei Zheng , Jianmin Zhang , John H. Zhang
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引用次数: 0

摘要

近年来,过氧化物酶体在中枢神经系统(CNS)中的作用越来越受到关注。本文就过氧化物酶体和噬磷脂在神经系统疾病中的生理病理机制作一综述。过氧化物酶体与线粒体、内质网和脂质体交流。它们的类型、大小和形状在大脑的不同区域各不相同。此外,过氧化物酶体在中枢神经系统的氧化稳态、脂质合成和降解中起重要作用,而其功能障碍可引起各种神经系统疾病。因此,选择性去除功能失调或多余的过氧化物酶体(噬酶)提供了神经保护作用,这表明了一个有希望的治疗靶点。然而,在神经系统疾病中,噬肉在很大程度上仍未被探索。棘噬在神经病理学中的串扰机制有待进一步研究。
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Peroxisome and pexophagy in neurological diseases
Peroxisomes and pexophagy have gained increasing attention in their role within the central nervous system (CNS) in recent years. In this review, we comprehensively discussed the physiological and pathological mechanisms of peroxisomes and pexophagy in neurological diseases. Peroxisomes communicate with mitochondria, endoplasmic reticulum, and lipid bodies. Their types, sizes, and shapes vary in different regions of the brain. Moreover, peroxisomes play an important role in oxidative homeostasis, lipid synthesis, and degradation in the CNS, whereas its dysfunction causes various neurological diseases. Therefore, selective removal of dysfunctional or superfluous peroxisomes (pexophagy) provides neuroprotective effects, which indicate a promising therapeutic target. However, pexophagy largely remains unexplored in neurological disorders. More studies are needed to explore the pexophagy's crosstalk mechanisms in neurological pathology.
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来源期刊
Fundamental Research
Fundamental Research Multidisciplinary-Multidisciplinary
CiteScore
4.00
自引率
1.60%
发文量
294
审稿时长
79 days
期刊介绍:
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