In vivo Analysis of DISABLED Function and Interactions in Synaptic Vesicle Cyclin
In vivo Analysis of DISABLED Function and Interactions in Synaptic Vesicle Cyclin
批准号:
8416446
负责人:
RICHARD W ORDWAY
金额:
$29.8万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-02-15 至 2015-01-31
关键词:
AddressAdultAffectBindingBiochemicalCaenorhabditis elegansCardiovascular DiseasesCell Surface ReceptorsChemicalsClathrinClathrin AdaptorsCyclinsDisabled PersonsDrosophila genusEndocytosisExhibitsFamilyFamily memberGene ProteinsGenesGeneticHealthHomologous GeneHumanImageIn VitroInvestigationLifeMapsMembraneMembrane ProteinsMolecularMolecular GeneticsMutationNeurosciencesNeurotransmittersPTB DomainPlayProcessPropertyProteinsRecyclingResearchRoleSecretory VesiclesSignal TransductionSorting - Cell MovementSurfaceSynapsesSynaptic TransmissionSynaptic VesiclesTemperatureTestingVesicleWorkcombatgenetic analysisin vivoinsightmembermutantnervous system disorderneuromuscularneurotransmitter releasenovelprotein distributionprotein functionrelating to nervous systemspatial relationshipsynaptic functiontrafficking
中文摘要
描述(由申请人提供):鉴于化学突触传递在正常和病理性神经活动中的至关重要性,对潜在机制的深入研究长期以来一直是并仍然是分子和细胞神经科学的主要焦点。更深入地了解突触传递的分子机制将对确定神经疾病过程和开发合理的治疗方法来对抗它们具有巨大的价值。拟议的研究建立在我们最近在果蝇中的遗传分析的基础上,该分析涉及突触囊泡内吞作用中的DISABLED(DAB)蛋白质-在神经递质与表面膜融合并释放其内容物后,使充满分泌囊泡的神经递质溶解的过程。部分原因是已知DAB在分选表面膜蛋白中起关键作用,并且与包括心血管疾病在内的主要人类健康状况有关,因此考虑这些蛋白质及其分子机制在突触传递中的另一种作用是令人兴奋的。以前还没有确定DABs在分选突触囊泡蛋白中的功能,但是现在提出的研究可能揭示了已经深入研究的一组DAB-dependent机制的重要突触连接。本项目将(1)建立在遗传分析的基础上,揭示突触传递中一种新的DAB相关机制,以确定dDAB在突触囊泡内吞作用的关键过程中的功能作用;(2)研究DAB蛋白的新功能与先前表征的突触囊泡内吞机制之间的联系,以更好地了解化学突触的组织和分子相互作用。传输
英文摘要
DESCRIPTION (provided by applicant): Given the critical importance of chemical synaptic transmission in normal and pathological neural activity, intensive investigation of the underlying mechanisms has long been and remains a primary focus in molecular and cellular neuroscience. Greater understanding of the molecular mechanisms of synaptic transmission will be of tremendous value in defining neurological disease processes and developing rational therapies to combat them. The proposed studies build on our recent genetic analysis in Drosophila implicating the DISABLED (DAB) proteins in the synaptic vesicle endocytosis - the process which recycles neurotransmitter filled secretory vesicles after they fuse with the surface membrane and release their contents. In part because DABs are known to play critical roles in sorting surface membrane proteins and have been implicated in major human health conditions including cardiovascular disease, it is exciting to consider another role for these proteins and their molecular mechanisms in synaptic transmission. A function for DABs in sorting synaptic vesicle proteins has not been identified previously, however the proposed studies may now reveal an important synaptic connection for an already intensively studied set of DAB-dependent mechanisms. This project will (1) build on genetic analysis implicating a novel DAB-related mechanism in synaptic transmission to define the functional role of dDAB in the critical process of synaptic vesicle endocytosis and (2) examine the connections between a new function for DAB proteins and previously characterized mechanisms of synaptic vesicle endocytosis to gain a better understanding of the organization and molecular interactions underlying chemical synaptic transmission.
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DOI:
10.1242/dmm.026385
发表时间:
2016-09-01
期刊:
Disease models & mechanisms
影响因子:
4.3
作者:
[Kawasaki F, Koonce NL, Guo L, Fatima S, Qiu C, Moon MT, Zheng Y, Ordway RW]
通讯作者:
Ordway RW
DOI:
10.1371/journal.pone.0017131
发表时间:
2011-02-16
期刊:
PloS one
影响因子:
3.7
作者:
[Danjo R, Kawasaki F, Ordway RW]
通讯作者:
Ordway RW
DOI:
10.1016/j.mcn.2011.02.002
发表时间:
2011-05
期刊:
MOLECULAR AND CELLULAR NEUROSCIENCE
影响因子:
3.5
作者:
[Yu, Wenhua, Kawasaki, Fumiko, Ordway, Richard W.]
通讯作者:
Ordway, Richard W.
DOI:
10.1371/journal.pone.0129957
发表时间:
2015
期刊:
PloS one
影响因子:
3.7
作者:
[Strauss AL, Kawasaki F, Ordway RW]
通讯作者:
Ordway RW
In vivo Analysis of DISABLED Function and Interactions in Synaptic Vesicle Cyclin
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批准号:7888923
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项目类别:
-
资助金额:$31.58万
-
财政年份:2010
-
负责人:RICHARD W ORDWAY
-
依托单位:
In vivo Analysis of DISABLED Function and Interactions in Synaptic Vesicle Cyclin
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批准号:8019482
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项目类别:
-
资助金额:$30.93万
-
财政年份:2010
-
负责人:RICHARD W ORDWAY
-
依托单位:
In vivo Analysis of DISABLED Function and Interactions in Synaptic Vesicle Cyclin
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批准号:8215786
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项目类别:
-
资助金额:$30.9万
-
财政年份:2010
-
负责人:RICHARD W ORDWAY
-
依托单位:
GENETIC AND FUNCTIONAL ANALYSIS OF SYNAPTIC TRANSMISSION
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批准号:6744160
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项目类别:
-
资助金额:$24.49万
-
财政年份:2001
-
负责人:RICHARD W ORDWAY
-
依托单位:
GENETIC AND FUNCTIONAL ANALYSIS OF SYNAPTIC TRANSMISSION
-
批准号:6266947
-
项目类别:
-
资助金额:$24.51万
-
财政年份:2001
-
负责人:RICHARD W ORDWAY
-
依托单位:
GENETIC AND FUNCTIONAL ANALYSIS OF SYNAPTIC TRANSMISSION
-
批准号:6639549
-
项目类别:
-
资助金额:$24.49万
-
财政年份:2001
-
负责人:RICHARD W ORDWAY
-
依托单位:
GENETIC AND FUNCTIONAL ANALYSIS OF SYNAPTIC TRANSMISSION
-
批准号:6540032
-
项目类别:
-
资助金额:$24.5万
-
财政年份:2001
-
负责人:RICHARD W ORDWAY
-
依托单位:
GENETIC ANALY OF NEUROTRANSMITTER RELEASE IN DROSOPHIA
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批准号:2261184
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项目类别:
-
资助金额:$1.42万
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财政年份:1995
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负责人:RICHARD W ORDWAY
-
依托单位:
MOLECULAR ANALYSIS--DROSOPHILA NEUROTRANSMITTER RELEASE
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批准号:2261183
-
项目类别:
-
资助金额:$2.99万
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财政年份:1993
-
负责人:RICHARD W ORDWAY
-
依托单位:
MOLECULAR ANALYSIS OF NEUROTRANSMITTER RELEASE IN DROSOP
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批准号:2261182
-
项目类别:
-
资助金额:$2.86万
-
财政年份:1993
-
负责人:RICHARD W ORDWAY
-
依托单位:
海外基金