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作 者:Debia Wakhloo Jane Oberhauser Angela Madira Sameehan Mahajani
机构地区:[1]Deparment of Neuropathology,Stanford University,School of Medicine,Stanford,CA,USA
出 处:《Neural Regeneration Research》2022年第12期2606-2614,共9页中国神经再生研究(英文版)
摘 要:Two of the most common neurodegenerative disorders-Alzheimer’s and Parkinson’s diseases-are characterized by synaptic dysfunction and degeneration that culminate in neuronal loss due to abnormal protein accumulation.The intracellular aggregation of hyper-phosphorylated tau and the extracellular aggregation of amyloid beta plaques form the basis of Alzheimer’s disease pathology.The major hallmark of Parkinson’s disease is the loss of dopaminergic neurons in the substantia nigra pars compacta,following the formation of Lewy bodies,which consists primarily of alpha-synuclein aggregates.However,the discrete mechanisms that contribute to neurodegeneration in these disorders are still poorly understood.Both neuronal loss and impaired adult neurogenesis have been reported in animal models of these disorders.Yet these findings remain subject to frequent debate due to a lack of conclusive evidence in post mortem brain tissue from human patients.While some publications provide significant findings related to axonal regeneration in Alzheimer’s and Parkinson’s diseases,they also highlight the limitations and obstacles to the development of neuroregenerative therapies.In this review,we summarize in vitro and in vivo findings related to neurogenesis,neuroregeneration and neurodegeneration in the context of Alzheimer’s and Parkinson’s diseases.
关 键 词:ALPHA-SYNUCLEIN amyloid beta plaques autophagy dopaminergic neurons human iPSCs mitochondrial dysfunction scRNA sequencing synaptic dysfunction Tau Wallerian degeneration
分 类 号:R742.5[医药卫生—神经病学与精神病学] R749.16[医药卫生—临床医学]
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