Activation and regulation of the neural stem cell-expressed receptor GPR56
Activation and regulation of the neural stem cell-expressed receptor GPR56
批准号:
8186265
负责人:
Randy A. Hall
金额:
$33.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-06-01 至 2016-02-29
关键词:
AdultAntibodiesBindingBrainBrain DiseasesCell physiologyCellsCiliaCleaved cellCustomDataDevelopmentEngineeringExhibitsGoalsHumanLigandsMapsMediatingModelingMolecularMusMutagenesisMutationN-terminalNerve DegenerationNeurodegenerative DisordersNeurogliaNeuronsOrganPathologyPeptide HydrolasesPeptidesPhysiologicalPlayProcessPropertyReceptor ActivationReceptor SignalingRegulationRoleSignal TransductionSignaling ProteinSiteSmall Interfering RNAStructureTestingTherapeuticWorkbasebeta-arrestincell motilitycell typedesignextracellulargamma secretasehuman GPRC5C proteininsightinterestmigrationnerve stem cellpeptidomimeticsreceptorreceptor functionrhoscaffoldsmall moleculesubventricular zonetherapeutic targettrafficking
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The orphan G protein-coupled receptor GPR56 is highly-expressed in neural stem cells (NSCs), and mutations in GPR56 cause disordered brain development in humans. The key role that GPR56 plays in NSC function makes it an attractive target for therapeutics that might be capable of highly-selective NSC modulation. However, little is currently known about the fundamental properties of GPR56. The specific targeting of GPR56 by therapeutics will require a more comprehensive understanding of the molecular mechanisms controlling receptor activation, regulation and localization. We will therefore study the mechanism of activation for GPR56, examining in particular the issue of whether shedding of the N-terminus (NT) is involved in receptor activation. We will also study the factors controlling GPR56-NT shedding, as well as whether receptor activation can be influenced by NT-binding peptides. Furthermore, we will assess the regulation of GPR56 activity by cytoplasmic binding partners of the receptor that have been identified in preliminary work, including beta-arrestins and PDZ scaffolds. Finally, we will study the factors controlling GPR56 localization in NSCs and other cell types, with a particular emphasis on determining the importance of receptor targeting to cilia. In addition to providing insights about the fundamental properties of GPR56, these studies will lay the groundwork for targeting GPR56 as a means of selectively modulating NSC function in the treatment of various neurodevelopmental and neurodegenerative diseases.
PUBLIC HEALTH RELEVANCE: The modulation of neural stem cells is a promising therapeutic approach in the treatment of various neurodevelopmental and neurodegenerative diseases. The orphan G protein-coupled receptor GPR56 is highly-expressed in neural stem cells and is therefore an attractive target for therapeutics that might be capable of highly-selective modulation of neural stem cell function. The proposed project will study GPR56 activation and regulation to lay the groundwork for potential therapeutic targeting of this receptor, which is expressed in neural stem cells.
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财政年份:2014
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财政年份:2014
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依托单位:
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财政年份:2012
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财政年份:2012
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Activation and regulation of the neural stem cell-expressed receptor GPR56
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批准号:8269907
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资助金额:$33.91万
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财政年份:2011
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负责人:Randy A. Hall
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依托单位:
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依托单位:
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依托单位:
PDZ scaffold regulation of astrocytic glutamate receptors and transporters
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资助金额:$29.91万
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财政年份:2008
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负责人:Randy A. Hall
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依托单位:
海外基金