Unfolded Protein Response in Alpha-synucleinopathies

α-突触核蛋白病中未折叠的蛋白质反应

• 批准号: 8990061
• 负责人: MICHAEL K LEE
• 金额: $ 33.33万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-01-15 至 2018-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8990061
• 关键词: Aging; Alzheimer' s Disease; Attenuated; Brain; CCAAT-Enhancer-Binding Proteins; Cell Death; Cells; Cellular biology; Chronic; Development; Disease; Dopamine; Etiology; Event; Exhibits; Functional disorder; Future; Genes; Genetic; Health; Homologous Protein; Human; In Vitro; Lead; Lewy Body Dementia; Link; Mind; Mitochondria; Modeling; Molecular; Molecular Abnormality; Molecular Biology; Multiple System Atrophy; Mus; Mutation; Nature; Nerve Degeneration; Neurodegenerative Disorders; Neurons; Oligodendroglia; Onset of illness; Oxidative Stress; PERK kinase; Parkinson Disease; Partner in relationship; Pathologic; Pathology; Pathway interactions; Pharmacological Treatment; Phosphoric Monoester Hydrolases; Phosphorylation; Property; Protein Dephosphorylation; Proteins; Quality Control; Reticulum; Rodent Model; Role; Specificity; Stress; Testing; Therapeutic Effect; Toxic effect; Transgenic Mice; Validation; age related; alpha synuclein; arm; attenuation; base; biological adaptation to stress; effective therapy; endoplasmic reticulum stress; genetic approach; in vivo; mitochondrial dysfunction; mouse model; neuropathology; neurotoxicity; new therapeutic target; novel; novel therapeutics; protein aggregation; protein degradation; response; stressor; synucleinopathy; targeted treatment; therapeutic target; therapy development

DESCRIPTION (provided by applicant): Alpha-synuclein abnormalities are implicated in a number of neurodegenerative diseases; including Parkinson's disease (PD), Lewy Body Dementia (LBD), and Multiple Systems Atrophy (MSA). Because alpha-synuclein aggregates in neurons (PD, LBD) and/or oligodendrocytes (MSA) are prominent pathological features of these diseases, they are categorized as alpha-synucleinopathies. Collectively, alpha-synucleinopathies represent the second most common late-onset neurodegenerative disease, next to Alzheimer's disease (AD). While there are no effective therapies that can slow or stop the progression of neurodegeneration associated with alpha-synucleinopathies, availability of multiple transgenic mouse models of various alpha-synucleinopathies allows us to better understand the genesis of alpha-synuclein abnormalities in vivo and mechanisms of neurodegeneration in brain. These efforts will likely lead to identifying novel therapeutic targets for alpha-synucleinopathies. Presence of intracellular alpha-synuclein aggregates in alpha-synucleinopathy suggest that some aspect of protein degradation/quality control is dysfunctional in the diseases. Consistent with this view, we found that neurodegeneration in cellular and transgenic mouse models of neuronal alpha-synucleinopathy is associated with chronic Endoplasmic Plasmic Reticulum Stress (ERS) with abnormal Unfolded Protein Response (UPR). Our studies indicate that ERS is initiated by translocation and aggregation of alpha-synuclein within the ER. More important, pharmacological treatment with an anti-ERS compound, Salubrinal, significantly delays disease manifestation in rodent model of neuronal alpha-synucleinopathy. These results suggest that ERS response pathway, particularly modulation of phospho-eIF2alpha levels could represent a novel therapeutic target for PD and other alpha-synucleinopathies. However, because of compounds such as Salubrinal may have unknown off-target effects in vivo, a rigorous validation the phospho-eIF2alpha as therapeutic target at molecular levels are needed. Further, it is not clear if all alpha-synucleinopathies shar common neurodegenerative mechanisms. With these issues in mind, we propose following studies. First, we will study whether chronic ERS is a general feature of alpha-synucleinopathy by studying ERS in both neuronal and glial alpha-synucleinopathies (PD, LBD, MSA). Second, we will determine if aging related factors, such as oxidative stress/mitochondrial dysfunction, promotes ER accumulation of alpha-synuclein oligomers. Finally, we will determine whether the genetic alterations in components of the Perk/eIF2alpha arm of the ERS have predictable effects on alpha-synuclein dependent neurodegeneration. These studies will establish the value of ER stress pathway, particularly Perk/eIF2alpha components, as targets for development of novel therapies for PD.

描述（由申请人提供）：α -突触核蛋白异常与许多神经退行性疾病有关；包括帕金森病（PD）、路易体痴呆（LBD）和多系统萎缩（MSA）。由于α -突触核蛋白聚集在神经元（PD， LBD）和/或少突胶质细胞（MSA）中是这些疾病的突出病理特征，因此它们被归类为α -突触核蛋白病。总的来说，α -突触核蛋白病是仅次于阿尔茨海默病（AD）的第二常见的迟发性神经退行性疾病。虽然目前还没有有效的治疗方法可以减缓或阻止与α -突触核蛋白病相关的神经退行性疾病的进展，但多种α -突触核蛋白病的转基因小鼠模型的可用性使我们能够更好地了解α -突触核蛋白异常在体内的发生和脑神经退行性疾病的机制。这些努力可能会导致发现新的治疗靶点