SIRT1 and the control of neuronal survival

SIRT1 和神经元存活的控制

• 批准号: 7893293
• 负责人: Santosh R D'Mello
• 金额: $ 21.88万
• 依托单位: UNIVERSITY OF TEXAS DALLAS
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-03-15 至 2012-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7893293
• 关键词: Apoptosis; Apoptotic; Biological Process; Cell Death; Cessation of life; Development; Enzymes; Family; Foundations; Goals; Histones; Human; Inhibition of Apoptosis; Investigation; Laboratories; Lead; Mass Spectrum Analysis; Mediating; Nature; Nerve Degeneration; Neurodegenerative Disorders; Neurons; Pathology; Patients; Proteins; Quality of life; Regulation; Research; Role; Signal Pathway; Signal Transduction Pathway; Sirtuins; Societies; Therapeutic; Work; cost; follow-up; insight; member; nervous system disorder; neuron apoptosis; neuron loss; neuronal survival; neuroprotection; novel; novel strategies; prevent; public health relevance; research study

DESCRIPTION (provided by applicant): A common feature of neurodegenerative diseases is the aberrant and excessive loss of neurons by activation of apoptosis. Numerous molecules involved in the promotion or inhibition of neuronal apoptosis have been identified and these are being organized as components of signal transduction pathways. This proposal focuses on sirtuins, a family of deacetylating enzymes that are the subject of intense investigation because of their role in a variety of different biological processes including the regulation of neurodegeneration. Like some other labs, we have found that one of the sirtuin proteins, SIRT1, protects neurons from apoptosis. But contrary to the conclusions of previous studies, we find that neuroprotection by SIRT1 is mediated by a novel, non-catalytic mechanism. The objective of the proposal is to use a multi- pronged approach to elucidate the novel mechanism by which SIRT1 exerts its neuroprotective action. The specific aims are - (1) to identify the region within SIRT1 that mediates neuroprotection, (2) to identify downstream targets and mechanism of SIRT1 action in neurons, and (3) to identify SIRT1-interacting proteins in neurons using mass-spectrometry. The long term goal of this research is to develop novel and effective strategies to prevent cell death in neurodegenerative pathologies. PUBLIC HEALTH RELEVANCE: Neurological diseases disrupt the quality of life for patients and cost society billions of dollars annually. While symptomatic treatments are available for many neurological diseases, a cure is not presently available. Identifying molecules that regulate neuronal survival and understanding the mechanism by which they act would lead to the development of more effective therapeutic strategies. Our proposal focuses on SIRT1, a protein that protects neurons from degeneration. It is our hope that the results from the studies we propose will shed insight into how SIRT1 exerts its neuroprotective effect and thus provide novel strategies to prevent neuronal loss in neurodegenerative conditions.

描述（由申请人提供）：神经退行性疾病的一个共同特征是细胞凋亡激活导致神经元的异常和过度损失。许多参与促进或抑制神经元凋亡的分子已经被确定，这些分子被组织为信号转导途径的组成部分。该建议侧重于sirtuins，这是一个脱乙酰酶家族，由于它们在各种不同的生物过程中发挥作用，包括神经退行性变的调节，因此受到了广泛的研究。像其他一些实验室一样，我们发现sirtuin蛋白之一SIRT1可以保护神经元免于凋亡。但与先前研究的结论相反，我们发现SIRT1的神经保护是通过一种新的非催化机制介导的。该建议的目的是使用多管齐下的方法来阐明SIRT1发挥其神经保护作用的新机制。具体目的是：(1)确定SIRT1中介导神经保护的区域，(2)确定SIRT1在神经元中作用的下游靶点和机制，以及(3)使用质谱法鉴定神经元中SIRT1相互作用的蛋白。本研究的长期目标是开发新颖有效的策略来预防神经退行性病变中的细胞死亡。