NMDA receptor trafficking by the autophagy regulatory protein beclin 1

通过自噬调节蛋白 beclin 1 进行 NMDA 受体转运

• 批准号: 8858700
• 负责人: EDWARD D PLOWEY
• 金额: $ 18.66万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-07-01 至 2019-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8858700
• 关键词: Activities of Daily Living; Aging; Alzheimer' s Disease; Amyloid beta-Protein; Autophagocytosis; Autophagosome; Binding; Biological Preservation; Brain; Caring; Catabolism; Cell Fractionation; Cell membrane; Clinical; Communities; Complex; Data; Degradation Pathway; Development Plans; Disease; Doctor of Medicine; Doctor of Philosophy; Educational workshop; Elderly; Electrophysiology (science); Environment; Equilibrium; Funding; Gene Expression; Genetic; Genetic Transcription; Glutamates; Goals; Grant; Health; Homeostasis; Huntington Disease; Impaired cognition; In Vitro; Ischemia; K-Series Research Career Programs; Knowledge; Laboratories; Learning; Link; Location; Manuscripts; Mediating; Medical; Mentors; Mentorship; Mitochondria; Molecular; Movement; Mus; N-Methyl-D-Aspartate Receptors; N-Methylaspartate; NR1 gene; Nerve Degeneration; Neurobiology; Neurodegenerative Disorders; Neurons; Outcome; Output; Pathologic; Pathology; Pathway interactions; Plant Roots; Positioning Attribute; Principal Investigator; Process; Program Development; Public Health; Receptor Activation; Regulation; Relative (related person); Research; Research Personnel; Research Proposals; Research Training; Role; Scientist; Secondary to; Services; Slice; Staging; Stress; Stress and Coping; Surface; Symptoms; Synapses; Synaptic Receptors; Techniques; Testing; Time; Toxic effect; Training Activity; Training Programs; Translating; United States National Institutes of Health; Universities; Vacuole; Vesicle; Work; Writing; age related neurodegeneration; base; career development; cognitive function; coping; coping mechanism; disease stressor; environmental stressor; experience; functional disability; genetic regulatory protein; improved; in vivo Model; injured; insight; interest; knowledge of results; medical schools; neurotoxicity; novel; patch clamp; professor; programs; protein aggregate; protein degradation; receptor; receptor internalization; research and development; restoration; skills; stressor; success; symposium; therapeutic target; trafficking

DESCRIPTION (provided by applicant): This K08 Mentored Clinician-Scientist Career Development Award application, entitled "NMDA Receptor Trafficking by the Autophagy Regulatory Protein Beclin 1", is submitted by Edward D. Plowey, M.D., Ph.D., Assistant Professor of Pathology at Stanford University School of Medicine. Dr. Plowey is a neuropathologist and clinician-scientist whose research interests lie in neurodegeneration and the mechanisms through which synapses and neurons cope with or succumb to neurodegenerative disease stressors. Dr. Plowey's immediate research goal is to investigate novel roles for autophagy in mediating adaptive synaptic adjustments to neurodegenerative disease stressors as the cornerstone of his independent research program. In this research proposal, a focus on beclin-dependent autophagy as a novel mechanism to regulate synaptic versus extra synaptic localization, subtype, internalization and degradation of NMDA receptors is proposed. He will test his hypothesis that beclin-dependent autophagy mediates neuroprotective modulation of NMDA receptor pools. In Aim 1 of this research proposal, the effects of synaptic versus extra synaptic NMDA receptor activation on beclin 1 levels, BECN1 gene expression and the capacity for neuroprotective beclin-dependent autophagy will be investigated. In the second Aim, the impact of beclin-deficiency on surface NMDA receptor levels, localization, subtype distribution and toxicity will be delineated. In Aim 3, the molecular basis, trafficking effects and modulatory effects of APP on beclin 1 interactions with NMDA receptors will be investigated, with a focus on the possibility that beclin 1 targets surface NR1/NR2B receptors for autophagolysosomal degradation by incorporation into plasma membrane derived autophagosomal precursor vesicles. Dr. Plowey will learn how autophagy modulates neuronal protein turnover and excitability secondary to synaptic perturbations and how beclin-dependent autophagy impacts NMDA receptor trafficking and the balance of synaptic and extra synaptic NMDA receptors. Furthermore, he will broaden our knowledge of the potential for beclin-dependent autophagy as a therapeutic target in neurodegeneration. Dr. Plowey's career development plan includes advanced research training in synaptic neurobiology techniques including receptor trafficking studies, patch clamp electrophysiology, organotypic slice cultures, subcellular fractionation approaches, molecular interaction studies and approaches to study the localization and functional outputs of synaptic and extra synaptic NMDA receptors. He will also engage in training activities to improve his grant writing and manuscript writing skills and increase his professional network and visibility in the scientific community through professional service, workshops and conferences. The collegial academic environment at Stanford University is ideal for the successful career development of clinician-scientists. Dr. Plowey has strong institutional commitment to his career development as an independent clinician-scientist from the Department of Pathology at Stanford University School of Medicine, which includes commitment of laboratory space, generous laboratory startup funds and 75% protected time to devote to his research program and career development activities. Furthermore, Dr. Plowey has established ideal mentor-prot�g� relationships with productive senior investigators with extensive mentorship experience in Tony Wyss-Coray, Ph.D. and Craig Garner, Ph.D. With a K08 Career Development Award to support his research and career development plans, Dr. Plowey will be positioned for success in his long term goals as a practicing neuropathologist and as a principal investigator of a sustainable NIH R01 funded research program in the synaptic neurobiology of neurodegeneration.

描述（由申请人提供）：本K 08指导临床医生-科学家职业发展奖申请，题为“自噬调节蛋白Beclin 1的NMDA受体贩运”，由Edward D. Plowey，医学博士，哲学博士、斯坦福大学医学院病理学助理教授。Plowey博士是一位神经病理学家和临床科学家，其研究兴趣在于神经退行性疾病以及突触和神经元科普或屈服于神经退行性疾病压力源的机制。Plowey博士的近期研究目标是研究自噬在介导神经退行性疾病压力源的适应性突触调整中的新作用，作为他独立研究计划的基石。在这项研究计划中，重点是beclin依赖性自噬作为一种新的机制，调节突触与突触外的定位，亚型，内化和降解的NMDA受体的建议。他将测试他的假设，即beclin依赖性自噬介导NMDA受体池的神经保护性调节。在本研究提案的目的1中，将研究突触与突触外NMDA受体激活对beclin 1水平、BECN 1基因表达和神经保护性beclin依赖性自噬能力的影响。在第二个目标中，将描述beclin缺乏对表面NMDA受体水平、定位、亚型分布和毒性的影响。在目标3中，分子 在此基础上，将研究APP对beclin 1与NMDA受体相互作用的运输效应和调节效应，重点是beclin 1通过掺入质膜衍生的自噬体前体囊泡而靶向表面NR 1/NR 2B受体进行自噬溶酶体降解的可能性。Plowey博士将了解自噬如何调节继发于突触扰动的神经元蛋白质周转和兴奋性，以及beclin依赖性自噬如何影响NMDA受体的运输以及突触和突触外NMDA受体的平衡。此外，他将扩大我们对beclin依赖性自噬作为神经变性治疗靶点的潜力的了解。Plowey博士的职业发展计划包括突触神经生物学技术的高级研究培训，包括受体运输研究，膜片钳电生理学，器官型切片培养，亚细胞分离方法，分子相互作用研究以及研究突触和突触外NMDA受体的定位和功能输出的方法。他还将参加培训活动，以提高他的赠款写作和手稿写作技能，并通过专业服务，研讨会和会议增加他的专业网络和在科学界的知名度。斯坦福大学的学术环境是临床科学家成功职业发展的理想选择。作为斯坦福大学医学院病理学系的独立临床科学家，Plowey博士对他的职业发展有着坚定的机构承诺，其中包括实验室空间的承诺、慷慨的实验室启动资金以及75%的受保护时间投入到他的研究计划和职业发展活动中。此外，Plowey博士与富有成效的高级研究人员建立了理想的导师-保护关系，他们在Tony Wyss-Coray博士那里拥有丰富的导师经验。和克雷格加纳博士通过K 08职业发展奖来支持他的研究和职业发展计划，Plowey博士将成功实现他作为执业神经病理学家的长期目标，并担任可持续NIH R 01资助的神经变性突触神经生物学研究项目的首席研究员。