Regulation of Clathrin-Coated Pits by the Mu-Opioid Receptor
Regulation of Clathrin-Coated Pits by the Mu-Opioid Receptor
批准号:
7447020
负责人:
Manojkumar A Puthenveedu
金额:
$7.44万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-06-01 至 2009-05-31
关键词:
AddressAffectAgonistBindingBiochemistryBrainC-terminalCell surfaceCellsCellular NeurobiologyCellular biologyClathrinCommitComplexConditionCritical PathwaysCytoplasmic TailCytoskeletonDependenceDevelopmentDiseaseDrug AddictionDrug Delivery SystemsDrug ToleranceElementsEndocytosisEnkephalin, Ala(2)-MePhe(4)-Gly(5)-EnkephalinsEventExcisionFamilyFutureG-Protein-Coupled ReceptorsLeadLifeLigandsLinkLocalizedMediatingMentorsMethadoneMitogen-Activated Protein KinasesMolecular GeneticsMorphineNeurobiologyNeuronsNeuropeptide ReceptorOpiate AddictionOpioidOpioid PeptideOpioid ReceptorPathologyPharmaceutical PreparationsPharmacologyPhysiologicalPlayProteinsProteomicsPublic HealthRateReceptor SignalingRegulationResearchRoleSignal PathwaySignal TransductionStagingSystemTestingTherapeuticTrainingVesicleWorkaddictionanalogbasecellular imagingclinically relevantcoated pitdelta opioid receptordesigndrug of abusegenetic regulatory proteinimprovedinsightmembermu opioid receptorsneuropsychiatrynovelopioid abusereceptorresearch studyresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Addiction to opioid drugs such as morphine is a major public health concern. The complex pathology of opioid addiction can be initiated by activation of specific drug targets in the brain, and the main target of abused drugs is the mu- opioid receptor (MOR), a member of the G protein-coupled receptor (GPCR) family. Activation of GPCRs elicits a sequence of events that results in regulated receptor removal from the cell surface by endocytosis. In the case of MOR, receptor endocytosis controls the de-sensitization and re-sensitization of the neuronal response to MOR signaling, and affects the long-term cellular changes that lead to the development of drug tolerance and dependence. While the traditional view is that regulation of receptor endocytosis is achieved by controlling receptor interaction with the endocytic machinery, my recent studies have identified a novel mechanism by which GPCRs, including MOR, specifically modulate their own endocytosis by controlling the local endocytic machinery. This suggests a novel and unanticipated facet of opioid regulation. The proposed studies seek to identify the mechanistic basis of this regulation and to investigate its functional significance to the effects of clinically relevant opioid drugs. Specifically, this proposal aims to: 1) identify structural determinants on MOR that mediate regulation of the endocytic machinery; 2) establish its mechanistic basis by identifying endocytic regulatory proteins; 3) determine the effect of different opioid drugs on this regulation in physiologically relevant neurons; and 4) define the functional consequences of this regulation on MOR signaling. CANDIDATE: The applicant has prior training in cell biology and biochemistry, and is committed to pursuing independent research in the cellular neurobiology of neuropsychiatric disorders and drug addiction. He will be mentored by Dr. Mark von Zastrow in the pharmacology, molecular genetics, and neurobiology of signaling receptors implicated in these disorders. RELEVANCE: The results of these studies will provide insight into a novel mode of regulation of a key opioid receptor, and improve our understanding of the development of drug tolerance and dependence. Thus they have the potential to serve as a platform for designing better and more informed therapeutic strategies against neuropsychiatric disorders and drug addiction. Further, the general principles defined will likely have broad implications to signaling events underlying a variety of pathological conditions.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1091/mbc.e17-01-0030
发表时间:
2017-08-01
期刊:
Molecular biology of the cell
影响因子:
3.3
作者:
[Shiwarski DJ, Darr M, Telmer CA, Bruchez MP, Puthenveedu MA]
通讯作者:
Puthenveedu MA
The association between law enforcement encounters and syringe sharing among IDUs on skid row: a mixed methods analysis.
执法遭遇与贫民窟注射吸毒者之间共用注射器之间的关联:混合方法分析。
DOI:
10.1007/s10461-013-0488-y
发表时间:
2013
期刊:
AIDS and behavior
影响因子:
4.4
作者:
[Wagner,KarlaD, Simon-Freeman,Rebecca, Bluthenthal,RickyN]
通讯作者:
Bluthenthal,RickyN
Divergent modes for cargo-mediated control of clathrin-coated pit dynamics.
网格蛋白包被的坑动力学的货物介导控制的不同模式。
DOI:
10.1091/mbc.e12-07-0550
发表时间:
2013
期刊:
Molecular biology of the cell
影响因子:
3.3
作者:
[Soohoo,AmandaL, Puthenveedu,ManojkumarA]
通讯作者:
Puthenveedu,ManojkumarA
Regulated trafficking and compartmentalized signaling of opioid receptors
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批准号:10529452
-
项目类别:
-
资助金额:$48.03万
-
财政年份:2022
-
负责人:Manojkumar A Puthenveedu
-
依托单位:
Cellular and Molecular Biology at Michigan
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批准号:10410595
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项目类别:
-
资助金额:$83.26万
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财政年份:2022
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负责人:Manojkumar A Puthenveedu
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依托单位:
Cellular and Molecular Biology at Michigan
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批准号:10650736
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项目类别:
-
资助金额:$84.89万
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财政年份:2022
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负责人:Manojkumar A Puthenveedu
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依托单位:
MECHANISMS ENSURING SEQUENCE-DEPENDENT GPCR RECYCLING
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批准号:9010148
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项目类别:
-
资助金额:$28.82万
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财政年份:2016
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负责人:Manojkumar A Puthenveedu
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依托单位:
Mechanisms Ensuring Sequence-Dependent GPCR Recycling
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批准号:9411123
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项目类别:
-
资助金额:$29.93万
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财政年份:2016
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负责人:Manojkumar A Puthenveedu
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依托单位:
TRAFFICKING AND FUNCTION OF MU-OPIOD RECEPTOR GENETIC VARIANTS
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批准号:8734364
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项目类别:
-
资助金额:$16.66万
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财政年份:2013
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负责人:Manojkumar A Puthenveedu
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依托单位:
TRAFFICKING AND FUNCTION OF MU-OPIOD RECEPTOR GENETIC VARIANTS
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批准号:8570648
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项目类别:
-
资助金额:$20.46万
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财政年份:2013
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负责人:Manojkumar A Puthenveedu
-
依托单位:
Regulation of Clathrin-Coated Pits by the Mu-Opioid Receptor
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批准号:7921680
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项目类别:
-
资助金额:$24.65万
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财政年份:2008
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负责人:Manojkumar A Puthenveedu
-
依托单位:
Regulation of Clathrin-Coated Pits by the Mu-Opioid Receptor
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批准号:7811163
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项目类别:
-
资助金额:$24.9万
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财政年份:2008
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负责人:Manojkumar A Puthenveedu
-
依托单位:
Regulation of Clathrin-Coated Pits by the Mu-Opioid Receptor
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批准号:8132904
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项目类别:
-
资助金额:$23.91万
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财政年份:2008
-
负责人:Manojkumar A Puthenveedu
-
依托单位:
Cellular and Molecular Biology at Michigan
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批准号:10194506
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项目类别:
-
资助金额:$72.95万
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财政年份:1975
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负责人:Manojkumar A Puthenveedu
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依托单位:
海外基金