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Circadian clock and dietary restriction

昼夜节律时钟和饮食限制

基本信息

批准号：
8523732
负责人：
Roman V Kondratov
金额：
$ 27.51万
依托单位：
CLEVELAND STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-09-15 至 2016-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8523732
关键词：
Address Adenosine Monophosphate Affect Age Aging Aging-Related Process Agreement Animals BMAL1 protein Behavior Brain Cells Circadian Rhythms Clock protein Complex Data Development Diabetes Mellitus Diet Disease Environment Feedback Glucose Heart Diseases Hour Human In Vitro Intake Intervention Invertebrates Life Liver Longevity Malignant Neoplasms Mammals Mediating Metabolism Molecular Mus Muscle Nutrient Organism Osteoporosis Pathology Pathway interactions Phosphorylation Physiological Physiology Plasma Post-Translational Protein Processing Premature aging syndrome Prevention Protein Kinase Proteins Regulation Resistance Risk Factors Role Signal Pathway Signal Transduction Staging Stress System Therapeutic Time Tissues Transcription Coactivator Transcription Repressor/Corepressor Up-Regulation Wild Type Mouse Yeasts base circadian pacemaker dietary restriction fly human FRAP1 protein in vivo innovation mimetics mutant novel therapy development treatment strategy

项目摘要

DESCRIPTION (provided by applicant): Dietary restriction (DR) is a powerful intervention, which slows the aging process and increases the lifespan of organisms, from yeast to mammals. The TOR signaling pathway is an evolutionarily conserved pathway implicated in the control of aging, and TOR is necessary for the full effect of DR. Hi95 /sestrin2 is a negative regulator of TOR pathways in mammals and invertebrates. We have found that Hi95/sestrin2 expression is significantly reduced in the brain, muscles and liver of BMAL1-deficient mice, and is increased in the same tissues of CRY-deficient mice; furthermore, BMAL1 deficiency results in up regulation of TOR signaling, suggesting that BMAL1 is a negative regulator of the TOR pathway. BMAL1 and CRYs are components of the circadian clock system. Thus, our preliminary data suggest a previously unknown interaction between the TOR signaling pathway and the circadian clock which may explain the role of the circadian clock in aging. We hypothesize that DR regulates the activity of the circadian clock proteins BMAL1 and CRYs, and these proteins mediate the effect of DR on longevity through the regulation of TOR pathways. We will address this hypothesis through the following Specific Aims: Aim 1. To study the molecular mechanisms of regulation of BMAL1 transcriptional activity by glucose. Aim 2. To investigate the role of the circadian clock proteins in the regulation of the Hi95-mTOR pathway. Aim 3. To study the role of the circadian clock and circadian clock proteins BMAL1 and CRYs in dietary restriction.

描述（由申请人提供）：饮食限制（DR）是一种强大的干预措施，可以减缓衰老过程并增加生物体的寿命，从酵母到哺乳动物。TOR信号通路是一种进化上保守的通路，与衰老的控制有关，TOR是DR的全部作用所必需的。Hi 95/sestrin 2是哺乳动物和无脊椎动物中TOR通路的负调节因子。我们已经发现，Hi 95/sestrin 2表达在BMAL 1缺陷小鼠的脑、肌肉和肝脏中显著降低，并且在BMAL 1缺陷小鼠的相同组织中增加;此外，BMAL 1缺陷导致TOR信号传导的上调，表明BMAL 1是TOR通路的负调节剂。BMAL 1和BMAL 2是生物钟系统的组成部分。因此，我们的初步数据表明TOR信号通路和生物钟之间存在一种以前未知的相互作用，这可能解释生物钟在衰老中的作用。我们假设DR调节生物钟蛋白BMAL 1和BMALS的活性，这些蛋白通过调节TOR通路介导DR对寿命的影响。我们将通过以下具体目标来解决这个假设：目标1。研究葡萄糖对BMAL 1转录活性调控的分子机制。目标二。研究生物钟蛋白在调节Hi 95-mTOR通路中的作用。目标3.研究生物钟和生物钟蛋白BMAL 1和BMAL s在饮食限制中的作用。