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线粒体神经退行性疾病:三种线粒体核糖体蛋白作为受损基因与阿尔茨海默病和帕金森病相关通路中的中间阶段。

Mitochondrial Neurodegenerative Diseases: Three Mitochondrial Ribosomal Proteins as Intermediate Stage in the Pathway That Associates Damaged Genes with Alzheimer's and Parkinson's.

作者信息

Del Giudice Luigi, Pontieri Paola, Aletta Mariarosaria, Calcagnile Matteo

机构信息

Istituto di Bioscienze e BioRisorse-UOS Napoli-CNR c/o Dipartimento di Biologia, Sezione di Igiene, 80134 Napoli, Italy.

DCSRSI SPR BIBLIOTECA, 80131 Napoli, Italy.

出版信息

Biology (Basel). 2023 Jul 8;12(7):972. doi: 10.3390/biology12070972.

DOI:10.3390/biology12070972
PMID:37508402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10376763/
Abstract

Currently, numerous research endeavors are dedicated to unraveling the intricate nature of neurodegenerative diseases. These conditions are characterized by the gradual and progressive impairment of specific neuronal systems that exhibit anatomical or physiological connections. In particular, in the last twenty years, remarkable efforts have been made to elucidate neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease. However, despite extensive research endeavors, no cure or effective treatment has been discovered thus far. With the emergence of studies shedding light on the contribution of mitochondria to the onset and advancement of mitochondrial neurodegenerative disorders, researchers are now directing their investigations toward the development of therapies. These therapies include molecules designed to protect mitochondria and neurons from the detrimental effects of aging, as well as mutant proteins. Our objective is to discuss and evaluate the recent discovery of three mitochondrial ribosomal proteins linked to Alzheimer's and Parkinson's diseases. These proteins represent an intermediate stage in the pathway connecting damaged genes to the two mitochondrial neurological pathologies. This discovery potentially could open new avenues for the production of medicinal substances with curative potential for the treatment of these diseases.

摘要

目前,众多研究致力于揭示神经退行性疾病的复杂本质。这些病症的特点是特定神经元系统逐渐且进行性受损,这些神经元系统呈现出解剖学或生理学联系。特别是在过去二十年里,人们为阐明诸如阿尔茨海默病和帕金森病等神经退行性疾病付出了巨大努力。然而,尽管进行了广泛的研究,但迄今为止尚未发现治愈方法或有效治疗手段。随着有关线粒体对线粒体神经退行性疾病的发生和发展所起作用的研究不断涌现,研究人员目前正将研究方向转向疗法的开发。这些疗法包括旨在保护线粒体和神经元免受衰老有害影响的分子,以及突变蛋白。我们的目标是讨论和评估最近发现的与阿尔茨海默病和帕金森病相关的三种线粒体核糖体蛋白。这些蛋白代表了受损基因与两种线粒体神经病理学之间联系途径中的一个中间阶段。这一发现有可能为生产具有治疗这些疾病潜在疗效的药物开辟新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a674/10376763/ce03c7cd6f67/biology-12-00972-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a674/10376763/be9615e443e6/biology-12-00972-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a674/10376763/ce03c7cd6f67/biology-12-00972-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a674/10376763/be9615e443e6/biology-12-00972-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a674/10376763/ce03c7cd6f67/biology-12-00972-g001.jpg

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The Mitochondrial tRNA Gene: A Novel m.7484A>G Mutation Associated with Mitochondrial Encephalomyopathy and Literature Review.线粒体tRNA基因:一种与线粒体脑肌病相关的新型m.7484A>G突变及文献综述
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