Mechanisms Specific to the Beneficial Effects of Dietary Restriction

饮食限制的有益作用的具体机制

• 批准号: 8741907
• 负责人: William B Mair
• 金额: $ 33.11万
• 依托单位: HARVARD SCHOOL OF PUBLIC HEALTH
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-30 至 2018-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8741907
• 关键词: 5' -AMP-activated protein kinase; Acute; Adult; Adverse effects; Age of Onset; Aging; Amino Acids; Animal Model; Animals; Biological Models; CREB1 gene; Caenorhabditis elegans; Cells; Data; Diagnosis; Diet; Disease; Disease Resistance; Eating; Gene Expression Profile; Genes; Genetic; Growth; Health; Human; Immunity; Intake; Intervention; Life; Link; Longevity; Longevity Pathway; Malnutrition; Mammals; Mediating; Mediator of activation protein; Methods; Mission; Molecular; Molecular Target; Neurons; Neurosecretory Systems; Nutrient; Nutritional; Outcome; Output; Pathology; Pathway interactions; Phosphorylation; Physiological; Process; Proteins; Public Health; Reproduction; Research; Role; Signal Transduction; Sirtuins; System; Testing; Therapeutic; Tissues; Transcript; Transcription Coactivator; United States National Institutes of Health; Work; age related; base; clinical application; cost; detection of nutrient; dietary restriction; endoplasmic reticulum stress; healthy aging; human FRAP1 protein; longevity gene; mortality; novel; novel therapeutics; prevent; public health relevance; reproductive; response; spatiotemporal; therapeutic target; trait; transcriptome sequencing

DESCRIPTION (provided by applicant): Dietary restriction (DR) is the most potent method for promoting healthy aging and age-onset disease resistance in animal models. However, DR's therapeutic potential is limited by associated negative physiological effects, including impaired growth, immunity and reproductive capacity. Although nutrient- sensing mediators of DR have been identified, such as mTOR, FOXO/As and the sirtuins, these central nodes recapitulate the entirety of the response, making them sub-optimal therapeutic targets. Our long-term objective is to uncover molecular mechanisms that specifically mediate only the pro-longevity effects of DR to develop optimal therapeutics. A key mediator of DR is AMP-activated protein kinase (AMPK), a cellular fuel gauge activated when energy levels are low. However, like DR, AMPK increases lifespan at the cost of impaired growth and reproduction. The objective in this application is to use the genetically tractable model system C. elegans to identify mechanisms by which AMPK specifically mediates longevity, in order to elucidate the first molecular targets that recapitulate only the pro-health effects of DR. The central hypothesis is that beneficial and detrimental effects of DR can be uncoupled. In support of this hypothesis, specific amino acid combinations in the diet have recently been shown to increase lifespan while maintaining normal reproduction, establishing that the positive effects of DR on lifespan do not require obligate detrimental side effects. However, the molecular mechanisms that uncouple longevity from associated negative effects are unknown. We have uncovered a longevity-specific target of AMPK, the 'CREB regulated transcriptional coactivator (CRTC)-1', that uncouples the longevity effects of AMPK from side effects. We now seek to identify the mechanisms by which CRTC-1 specifically mediates longevity. The rationale for this project is that, before we can generate viable therapies from DR for clinical application we must first identify mechanisms that 1) recapitulate only the positive effects of DR and 2) are effective when applied late in life, post-diagnosis of age- related disease. Based upon strong preliminary data we will test three specific aims. 1) We will examine the role of CRTC-1 in promoting healthy aging via increases to protein fidelity checkpoints. 2) We will utilize a novel inducible system to identify DR mediators with acute, late-onset beneficial effects and 3) We will define the longevity-specific transcriptome regulated by CRTC-1, to determine molecular targets that specifically promote healthy aging without physiological side effects. Collectively, we expect this work to provide the first example of molecular pathways that uncouple the positive and negative effects of DR, a critical step in transitioning DR research to the promotion of healthy human aging.

描述（由申请人提供）：饮食限制（DR）是在动物模型中促进健康衰老和年龄发病抵抗力的最有效方法。然而，DR的治疗潜力受到相关负面生理效应的限制，包括生长、免疫和生殖能力受损。尽管已经鉴定了DR的营养物敏感介质，例如mTOR、F0 X 0/As和沉默调节蛋白，但这些中心节点概括了整个反应，使其成为次优治疗靶标。我们的长期目标是揭示仅特异性介导DR的促长寿效应的分子机制，以开发最佳治疗方法。DR的关键介质是AMP活化蛋白激酶（AMPK），这是一种在能量水平低时激活的细胞燃料计量器。然而，与DR一样，AMPK以受损的生长和繁殖为代价延长寿命。本申请的目的是使用遗传上易处理的模型系统C。elegans来确定AMPK特异性介导长寿的机制，以阐明第一个分子靶点，该靶点仅概括DR的促健康作用。中心假设是DR的有益和有害作用可以解耦。为了支持这一假设，饮食中的特定氨基酸组合最近被证明可以增加寿命，同时保持正常的生殖，这表明DR对寿命的积极影响不需要强制性的有害副作用。然而，将长寿与相关的负面影响分开的分子机制尚不清楚。我们已经发现了AMPK的长寿特异性靶点，即“CREB调节的转录辅激活因子（CRTC）-1”，它将AMPK的长寿效应与副作用分开。我们现在试图确定CRTC-1特异性介导长寿的机制。该项目的基本原理是，在我们可以从DR产生可行的治疗方法用于临床应用之前，我们必须首先确定以下机制：1）仅概括DR的积极作用，2）在年龄相关疾病诊断后的晚期应用时有效。基于强有力的初步数据，我们将测试三个具体目标。1)我们将研究CRTC-1通过增加蛋白质保真度检查点在促进健康衰老中的作用。2)我们将利用一种新的诱导系统来鉴定具有急性、迟发性有益作用的DR介导物，3）我们将定义由CRTC-1调节的长寿特异性转录组，以确定特异性促进健康衰老而无生理副作用的分子靶点。总的来说，我们希望这项工作能够提供第一个将DR的积极和消极影响分开的分子途径的例子，这是将DR研究转变为促进健康人类衰老的关键一步。