Effect of aging on enteric neural stem cells is dependent on the PI3K/Akt pathway

衰老对肠神经干细胞的影响取决于 PI3K/Akt 通路

• 批准号: 8556711
• 负责人: Laren Becker
• 金额: $ 7.88万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-08-15 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8556711
• 关键词: Accounting; Address; Adult; Affect; Age; Aging; Aging-Related Process; Animals; Anorexia; Anus; Apoptosis; Biological Neural Networks; Caloric Restriction; Cell Aging; Cell physiology; Cells; Cognitive; Colon; Constipation; Data; Disease; Elderly; Enteral; Enteric Nervous System; Environment; Equilibrium; Esophagus; Etiology; Fecal Incontinence; Flow Cytometry; Foundations; Future; Gastrointestinal Diseases; Gastrointestinal Motility; Gastrointestinal Physiology; Goals; Health; Health Care Costs; Human; Impaired cognition; In Vitro; Institution; Intestines; Knowledge; Lead; Mediating; Molecular Target; Motor; Motor Neurons; Mus; Muscle; Myenteric Plexus; Myofibroblast; Nervous system structure; Neuraxis; Neuritis; Neuroglia; Neurons; Nitrergic Neurons; Nitrogen; Oxidative Stress; Oxygen; Pathway interactions; Phenotype; Physiological; Play; Population; Process; Quality of life; Relative (related person); Research; Research Personnel; Resources; Rodent; Role; Signal Pathway; Societies; Stem cells; Stomach; Testing; Transplantation; Vitamin A; Work; age effect; age related; aged; base; career; cell age; cell motility; cholinergic; cholinergic neuron; excitatory neuron; experience; functional loss; gastrointestinal; gastrointestinal function; health care quality; improved; in vivo; inhibitor/antagonist; inhibitory neuron; nerve stem cell; neuron loss; neuroregulation; prevent; research study; senescence; skills

DESCRIPTION (provided by applicant): Aging causes physiologic changes in gastrointestinal intestinal function that contribute to many age-related disorders. These disorders cause a significant burden both in healthcare costs and quality of life. A shift in the ratio of motor neurons favoring inhibitory (nitrergic) neurons over excitatory (cholinergic) neurons has been observed in the ENS with aging and is thought to play an important role in these disorders. While many have speculated that 'wear and tear' resulting from oxidative stress is the cause for this disturbance, the mechanism(s) underlying the effects of aging on the ENS are poorly understood. Aging is increasingly viewed as a highly regulated process. In the central nervous system (CNS), there is evidence that loss of functional neural stem cells contributes to the aging process and cognitive decline. Similar decline in stem cell function may also be contributing to age-related changes in the ENS. The goal of the proposed research is to study the effect of aging on a population of neural stem cells in the ENS, termed enteric neural stem cells (ENSCs). Recent work by the candidate suggests that ENSCs from old mice differentiate into cells that express higher levels of nNOS, a marker of nitrergic neurons, than those from young mice and that this difference may be due to higher basal Akt activity found in ENS from old mice. The candidate hypothesizes that age-related disturbances in the ENS are due to alterations in ENSC function mediated by the PI3K/Akt/FOXO pathway. The candidate plans to address this hypothesis in two ways. First, the candidate will delineate intrinsic differences in ENSCs isolated by flow cytometry from old and young mice. Specifically, the candidate will perform experiments to evaluate for differences with regards to proliferation, apoptosis, senescence, and differentiation using both in vitro and in vivo (transplantation) approaches. Second, the candidate will investigate the role of the PI3K/Akt/FOXO3 signaling pathway in the aging process in ENSCs. Specifically, the candidate will assess the basal activity of the PI3K/Akt/FOXO3 pathway in old and young ENSCs and evaluate how modulating this pathway through stimulation and inhibition affects their phenotypes. These studies will enhance our understanding of aging in the ENS and lay the foundation for future research including: 1) determining whether caloric-restriction reverses age-related changes to ENSC function, 2) evaluating whether similar age-related changes occur in human ENSCs, and 3) elucidating molecular targets that will reverse the effect of aging on ENSCs. The candidate believes that Stanford, a world-class institution with particular strength in stem cell and aging research, is th ideal environment for developing his academic career. With Dr. Anne Brunet as his senior collaborator, the abundant resources available at Stanford, and a wide range of didactics to broaden his scientific knowledge and technical skills, the candidate is uniquely placed to pursue his goal of becoming an independent investigator.

描述（由申请人提供）：衰老导致胃肠道功能的生理变化，导致许多与年龄相关的疾病。这些疾病在医疗费用和生活质量方面造成了重大负担。在ENS中观察到，随着年龄的增长，运动神经元的比例倾向于抑制性（氮能）神经元而不是兴奋性（胆碱能）神经元，这被认为在这些疾病中起着重要作用。虽然许多人推测由氧化应激引起的“磨损”是造成这种紊乱的原因，但人们对衰老对ENS影响的潜在机制知之甚少。老龄化越来越被视为一个高度调控的过程。在中枢神经系统（CNS）中，有证据表明功能性神经干细胞的丧失有助于衰老过程和认知能力下降。干细胞功能的类似下降也可能导致ENS中与年龄相关的变化。拟议研究的目标是研究衰老对ENS中神经干细胞群体的影响，称为肠内神经干细胞（ENSCs）。该候选人最近的研究表明，与年轻小鼠相比，老年小鼠的ENSCs分化为表达更高水平nNOS（一种氮能神经元标记物）的细胞，这种差异可能是由于老年小鼠ENS中发现了更高的基础Akt活性。候选人假设ENS中与年龄相关的紊乱是由于PI3K/Akt/FOXO通路介导的ENSC功能改变。候选人计划用两种方式来解决这个假设。首先，候选人将描述通过流式细胞术从老年和年轻小鼠中分离的ENSCs的内在差异。具体来说，候选人将通过体外和体内（移植）方法进行实验，评估在增殖、细胞凋亡、衰老和分化方面的差异。其次，候选人将研究PI3K/Akt/FOXO3信号通路在ENSCs衰老过程中的作用。具体而言，候选人将评估老年和年轻ENSCs中PI3K/Akt/FOXO3通路的基础活性，并评估通过刺激和抑制调节该通路如何影响其表型。这些研究将增强我们对enc衰老的理解，并为未来的研究奠定基础，包括：1)确定热量限制是否逆转年龄相关的enc功能变化，2)评估人类ENSC是否发生类似的年龄相关变化，以及3)阐明逆转衰老对ENSC影响的分子靶点。候选人认为，斯坦福大学是一个世界级的机构，在干细胞和衰老研究方面具有特别的优势，是他发展学术生涯的理想环境。Anne Brunet博士是他的高级合作伙伴，斯坦福大学丰富的资源，以及广泛的教学，以扩大他的科学知识和技术技能，候选人是追求他成为一名独立研究者的目标的独特条件。