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作 者:Wenzhi Chen Shishi Jiang Shu Li Cheng Li Renshi Xu
出 处:《Neural Regeneration Research》2024年第11期2513-2521,共9页中国神经再生研究(英文版)
基 金:supported by the National Natural Science Foundation of China,Nos.30560042,81160161,81360198,82160255;a grant from Department of Education of Jiangxi Province,Nos.GJJ13198,GJJ170021;Jiangxi Provincial Department of Science and Technology,Nos.[2014]-47,20142BBG70062,20171BAB215022,20192BAB205043;Science and Technology Plan of Jiangxi Commission of Health,Nos.202210002,202310119(all to RX).
摘 要:Amyotrophic lateral sclerosis is a neurodegenerative disease,and the molecular mechanism underlying its pathology remains poorly understood.However,inflammation is known to play an important role in the development of this condition.To identify driver genes that affect the inflammatory response in amyotrophic lateral sclerosis,as well as potential treatment targets,it is crucial to analyze brain tissue samples from patients with both sporadic amyotrophic lateral sclerosis and C9orf72-related amyotrophic lateral sclerosis.Therefore,in this study we used a network-driven gene analysis tool,NetBID2.0,which is based on SJARACNe,a scalable algorithm for the reconstruction of accurate cellular networks,to experimentally analyze sequencing data from patients with sporadic amyotrophic lateral sclerosis.The results showed that the OSMR gene is pathogenic in amyotrophic lateral sclerosis and participates in the progression of amyotrophic lateral sclerosis by mediating the neuroinflammatory response.Furthermore,there were differences in OSMR activity and expression between patients with sporadic amyotrophic lateral sclerosis and those with C9orf72-related amyotrophic lateral sclerosis.These findings suggest that OSMR may be a diagnostic and prognostic marker for amyotrophic lateral sclerosis.
关 键 词:amyotrophic lateral sclerosis DRIVER NEUROINFLAMMATION OSMR C9ORF72 neurodegenerative disease PATHOGENESIS oxidative stress protein misfolding mitochondrial dysfunction
分 类 号:R744.8[医药卫生—神经病学与精神病学]
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