Hashimoto Makoto, Rockenstein Edward, Crews Leslie, Masliah Eliezer
Department of Neurosciences, University of California, San Diego, La Jolla, CA 92093-0624, USA.
Neuromolecular Med. 2003;4(1-2):21-36. doi: 10.1385/NMM:4:1-2:21.
Abnormal interactions and misfolding of synaptic proteins in the nervous system are being extensively explored as important pathogenic events resulting in neurodegeneration in various neurological disorders. These include Alzheimer's disease (AD), Parkinson's disease (PD), and dementia with Lewy bodies (DLB). In AD, misfolded amyloid beta peptide 1-42 (Abeta), a proteolytic product of amyloid precursor protein metabolism, accumulates in the neuronal endoplasmic reticulum and extracellularly as plaques. In contrast, in PD and DLB cases there is abnormal accumulation of alpha-synuclein in neuronal cell bodies, axons, and synapses. Furthermore, in DLB, Abeta 1-42 may promote alpha-synuclein accumulation and neurodegeneration. The central event leading to synaptic and neuronal loss in these diseases is not completely clear yet; however, recent advances in the field suggest that nerve damage might result from the conversion of nontoxic monomers to toxic oligomers and protofibrils. The mechanisms by which misfolded Abeta peptide and alpha-synuclein might lead to synapse loss are currently under investigation. Several lines of evidence support the possibility that Abeta peptide and alpha-synuclein might interact to cause mitochondrial and plasma membrane damage upon translocation of protofibrils to the membranes. Accumulation of Abeta and alpha-synuclein oligomers in the mitochondrial membrane might result in the release of cytochrome C with the subsequent activation of the apoptosis cascade. Conversely, the oxidative stress and mitochondrial dysfunction associated with AD and PD may also lead to increased membrane permeability and cytochrome C release, which promotes Abeta and alpha-synuclein oligomerization and neurodegeneration. Together, these studies suggest that the translocation of misfolded proteins to the mitochondrial membrane might play an important role in either triggering or perpetuating neurodegeneration. The insights obtained from the characterization of this process may be applied to the role of mitochondrial dysfunction in other neurodegenerative disorders, including AD. New evidence may also provide a rationale for the mitochondrial membrane as a target for therapy in a variety of neurodegenerative diseases.
神经系统中突触蛋白的异常相互作用和错误折叠作为导致各种神经疾病神经退行性变的重要致病事件正被广泛研究。这些疾病包括阿尔茨海默病(AD)、帕金森病(PD)和路易体痴呆(DLB)。在AD中,淀粉样前体蛋白代谢的蛋白水解产物——错误折叠的淀粉样β肽1-42(Aβ),在神经元内质网中积累并在细胞外形成斑块。相比之下,在PD和DLB病例中,α-突触核蛋白在神经元细胞体、轴突和突触中异常积累。此外,在DLB中,Aβ 1-42可能促进α-突触核蛋白的积累和神经退行性变。导致这些疾病中突触和神经元丧失的核心事件尚不完全清楚;然而,该领域的最新进展表明,神经损伤可能是由无毒单体转化为有毒寡聚体和原纤维所致。错误折叠的Aβ肽和α-突触核蛋白导致突触丧失的机制目前正在研究中。几条证据支持Aβ肽和α-突触核蛋白可能相互作用,在原纤维转移到膜上时导致线粒体和质膜损伤的可能性。Aβ和α-突触核蛋白寡聚体在线粒体膜中的积累可能导致细胞色素C的释放,随后激活凋亡级联反应。相反,与AD和PD相关的氧化应激和线粒体功能障碍也可能导致膜通透性增加和细胞色素C释放,从而促进Aβ和α-突触核蛋白寡聚化和神经退行性变。总之,这些研究表明错误折叠的蛋白质转移到线粒体膜上可能在引发或延续神经退行性变中起重要作用。从该过程的特征中获得的见解可能适用于线粒体功能障碍在包括AD在内的其他神经退行性疾病中的作用。新证据也可能为将线粒体膜作为多种神经退行性疾病的治疗靶点提供理论依据。