Optical study of secretion in mammalian nerve terminals
哺乳动物神经末梢分泌的光学研究
基本信息
- 批准号:8295121
- 负责人:
- 金额:$ 49.75万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-07-24 至 2017-02-28
- 项目状态:已结题
- 来源:
- 关键词:Alzheimer&aposs DiseaseAmplifiersArgipressinAtomic Force MicroscopyAxonBiological ProcessBlood CirculationCell physiologyCellsClinicCollectionCouplingDetectionDevelopmentDiseaseElectron MicroscopyEquilibriumEventExocytosisExtracellular SpaceFiberFluorescenceGoalsGoldHormonesHypertensionHypothalamic structureImmune responseImpairmentIn VitroInfundibular StalkLaboratoriesLambert-Eaton Myasthenic SyndromeLeadMeasurementMechanicsMembraneMembrane FusionMental DepressionMetabolicMetabolismMethodsMilk EjectionMitochondriaMoodsMusNADHNamesNerveNervous system structureNeurologicNeuronsNeuropeptidesNeurosecretionOptical MethodsOpticsOxytocinPhysiologicalPituitary GlandPosterior Pituitary GlandPreparationProcessProteinsRegulationReproductionResolutionScanning Probe MicroscopesSchizophreniaSecretory VesiclesSex BehaviorSignal TransductionStagingSynaptic TransmissionSystemTechniquesTechnologyTemperatureTestingTimeTransgenic MiceVariantVasopressinsWaterbaseblood pressure regulationcell motilitycoraldetectorfluorophoreinformation processinginsightlight scatteringmagnocellularmedian eminencemillisecondneurotransmitter releasenovelnovel strategiesparaventricular nucleuspeptide hormonepresynapticpromoterred fluorescent proteinresearch studyresponsesocial cognitionsupraoptic nucleustool
项目摘要
DESCRIPTION (provided by applicant): Secretion is one of the most ubiquitous of cellular processes. Regulated exocytosis is central to such diverse biological functions as information processing, reproduction, motility, temperature regulation, metabolism, the immune response, and signal transduction, but the elucidation of its mechanism(s) remains a challenge to cell physiologists. The neurohypophysis is a classic in vitro preparation, uniquely relevant for studying evoked release of peptide hormones. Magnocellular neurons from the supraoptic and paraventricular nuclei in the hypothalamus project their axons as bundles of fibers through the median eminence and infundibular stalk to arborize extensively and terminate in the neurohypophysis, a quasi-pure collection of nerve terminals, where the neuropeptides oxytocin and vasopressin are released into the circulation. Despite remarkable progress in identifying components of the macromolecular machinery essential for their release, direct observation in real time of the intraterminal events that follow electrical excitation, but precede membrane fusion, has proven extremely difficult. To identify these steps we have developed an arsenal of biophysical techniques possessing time scales ranging from microseconds to minutes, with emphasis on the former. Three of them, in particular, constitute the core of each of our specific aims: 1) High Bandwidth Dynamic Atomic Force Microscopy (HBDAFM), to study the rapid, but very small (~1.0 ¿), mechanical events ("spike" and "dip") which accompany neuropeptide secretion in mammalian nerve terminals. 2) Real-time detection of Ca2+-transients, from whole terminals as well as from near- membrane regions, to identify intermediate steps between Ca2+-entry and exocytosis. 3) Millisecond time resolved optical detection of secretion per se. These technologies, already at different stages of development in our laboratory, will be combined in this proposal to capture, in a single experiment, sequential, albeit partially overlapping events, which are essential components of excitation-secretion coupling.
PUBLIC HEALTH RELEVANCE: The hormones secreted by the neurohypophysis, oxytocin and vasopressin, are implicated in functions as diverse as blood pressure regulation, water balance, milk ejection, social cognition, sexual behavior, and mood control. Therefore, greater insight into arginine vasopressin exocytosis, for example, may enhance our ability to treat hypertension~ furthermore, since many neurological ailments involve an impairment of neurotransmitter release, advancing our understanding of its presynaptic component is key to the development of new approaches to the treatment of disorders of synaptic transmission implicated in ailments as devastating as, to name a few, Lambert-Eaton Syndrome, schizophrenia, Alzheimer's disease and depression.
描述(由申请人提供):分泌是最普遍的细胞过程之一。受调节的胞吐作用在信息处理、生殖、运动、温度调节、代谢、免疫应答和信号转导等多种生物学功能中起着重要作用,但其机制的阐明仍然是细胞生理学家面临的一个挑战。神经垂体是一个经典的体外制备,独特的相关研究肽类激素的诱发释放。来自下丘脑视上核和室旁核的大细胞神经元将其轴突投射为纤维束,穿过正中隆起和漏斗柄,以广泛地分支并终止于神经垂体,神经垂体是神经末梢的准纯集合,其中神经肽催产素和加压素被释放到循环中。尽管在识别大分子机械的释放所必需的组分方面取得了显着进展,但在真实的时间内直接观察电激发之后但在膜融合之前的终末内事件已被证明是极其困难的。为了确定这些步骤,我们开发了一个生物物理技术的武器库,拥有从微秒到分钟的时间尺度,重点放在前者。其中三个,特别是,构成了我们每个具体目标的核心:1)高带宽动态原子力显微镜(HBDAFM),研究快速,但非常小(~1.0 <$),机械事件(“尖峰”和“下降”)伴随着哺乳动物神经末梢的神经肽分泌。2)实时检测整个末端以及近膜区域的Ca 2+瞬变,以识别Ca 2+进入和胞吐之间的中间步骤。3)分泌物本身的毫秒时间分辨光学检测。这些技术,已经在不同的发展阶段,在我们的实验室,将结合在这个建议,在一个单一的实验中,捕捉顺序,虽然部分重叠的事件,这是兴奋分泌耦合的重要组成部分。
公共卫生相关性:由神经垂体分泌的激素,催产素和加压素,涉及多种功能,如血压调节,水平衡,乳汁排出,社会认知,性行为和情绪控制。因此,更深入地了解精氨酸加压素胞吐作用,例如,可以提高我们治疗高血压的能力。此外,由于许多神经系统疾病涉及神经递质释放的损伤,因此提高我们对其突触前组分的理解是开发治疗突触传递障碍的新方法的关键,这些疾病涉及破坏性疾病,例如Lambert-Eaton综合征,精神分裂症、阿尔茨海默病和抑郁症。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
BRIAN Matthew SALZBERG其他文献
BRIAN Matthew SALZBERG的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('BRIAN Matthew SALZBERG', 18)}}的其他基金
Optical Study of Secretion in Mammalian Nerve Terminals
哺乳动物神经末梢分泌物的光学研究
- 批准号:
6759446 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical study of secretion in mammalian nerve terminals
哺乳动物神经末梢分泌的光学研究
- 批准号:
9004654 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical Study of Secretion in Mammalian Nerve Terminals
哺乳动物神经末梢分泌物的光学研究
- 批准号:
6540374 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical Study of Secretion in Mammalian Nerve Terminals
哺乳动物神经末梢分泌物的光学研究
- 批准号:
6400136 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical Study of Secretion in Mammalian Nerve Terminals
哺乳动物神经末梢分泌物的光学研究
- 批准号:
6612613 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical Study of Secretion in Mammalian Nerve Terminals
哺乳动物神经末梢分泌物的光学研究
- 批准号:
6917143 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical study of secretion in mammalian nerve terminals
哺乳动物神经末梢分泌的光学研究
- 批准号:
8431349 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical study of secretion in mammalian nerve terminals
哺乳动物神经末梢分泌的光学研究
- 批准号:
8611749 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
Optical study of secretion in mammalian nerve terminals
哺乳动物神经末梢分泌的光学研究
- 批准号:
7895768 - 财政年份:2001
- 资助金额:
$ 49.75万 - 项目类别:
MULTIPLE SITE OPTICAL RECORDING OF MEMBRANE POTENTIAL
膜电位的多位点光学记录
- 批准号:
3397167 - 财政年份:1980
- 资助金额:
$ 49.75万 - 项目类别:
相似国自然基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
- 批准号:81000622
- 批准年份:2010
- 资助金额:20.0 万元
- 项目类别:青年科学基金项目
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
- 批准号:31060293
- 批准年份:2010
- 资助金额:26.0 万元
- 项目类别:地区科学基金项目
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究
- 批准号:30960334
- 批准年份:2009
- 资助金额:22.0 万元
- 项目类别:地区科学基金项目
相似海外基金
Pathophysiological mechanisms of hypoperfusion in mouse models of Alzheimer?s disease and small vessel disease
阿尔茨海默病和小血管疾病小鼠模型低灌注的病理生理机制
- 批准号:
10657993 - 财政年份:2023
- 资助金额:
$ 49.75万 - 项目类别:
Social Connectedness and Communication in Parents with Huntington''s Disease and their Offspring: Associations with Psychological and Disease Progression
患有亨廷顿病的父母及其后代的社会联系和沟通:与心理和疾病进展的关联
- 批准号:
10381163 - 财政年份:2022
- 资助金额:
$ 49.75万 - 项目类别:
The Role of Menopause-Driven DNA Damage and Epigenetic Dysregulation in Alzheimer s Disease
更年期驱动的 DNA 损伤和表观遗传失调在阿尔茨海默病中的作用
- 批准号:
10531959 - 财政年份:2022
- 资助金额:
$ 49.75万 - 项目类别:
The Role of Menopause-Driven DNA Damage and Epigenetic Dysregulation in Alzheimer s Disease
更年期驱动的 DNA 损伤和表观遗传失调在阿尔茨海默病中的作用
- 批准号:
10700991 - 财政年份:2022
- 资助金额:
$ 49.75万 - 项目类别:
Interneurons as early drivers of Huntington´s disease progression
中间神经元是亨廷顿病进展的早期驱动因素
- 批准号:
10518582 - 财政年份:2022
- 资助金额:
$ 49.75万 - 项目类别:
Interneurons as Early Drivers of Huntington´s Disease Progression
中间神经元是亨廷顿病进展的早期驱动因素
- 批准号:
10672973 - 财政年份:2022
- 资助金额:
$ 49.75万 - 项目类别:
Social Connectedness and Communication in Parents with Huntington''s Disease and their Offspring: Associations with Psychological and Disease Progression
患有亨廷顿病的父母及其后代的社会联系和沟通:与心理和疾病进展的关联
- 批准号:
10585925 - 财政年份:2022
- 资助金额:
$ 49.75万 - 项目类别:
Oligodendrocyte heterogeneity in Alzheimer' s disease
阿尔茨海默病中的少突胶质细胞异质性
- 批准号:
10180000 - 财政年份:2021
- 资助金额:
$ 49.75万 - 项目类别:
Serum proteome analysis of Alzheimer´s disease in a population-based longitudinal cohort study - the AGES Reykjavik study
基于人群的纵向队列研究中阿尔茨海默病的血清蛋白质组分析 - AGES 雷克雅未克研究
- 批准号:
10049426 - 财政年份:2021
- 资助金额:
$ 49.75万 - 项目类别:
Repurposing drugs for Alzheimer´s disease using a reverse translational approach
使用逆翻译方法重新利用治疗阿尔茨海默病的药物
- 批准号:
10295809 - 财政年份:2021
- 资助金额:
$ 49.75万 - 项目类别: