Temperature-activated TRP channels and thermosensation
Temperature-activated TRP channels and thermosensation
批准号:
7222657
负责人:
Ardem Patapoutian
金额:
$40.76万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-04-01 至 2010-03-31
关键词:
AcuteAddressAfferent NeuronsBehavioralBehavioral AssayBiochemical GeneticsBiological AssayCamphorCapsaicinCellsChemicalsChromosome PairingCodeDataEngineeringEpidermisEsthesiaGenesGoalsHearingHeatingHomologous GeneInvestigationIon ChannelKnock-outKnockout MiceLinkMechanicsMediatingModalityMolecularMusNerveNerve EndingsNerve FibersNervous system structureNeuritesNeurobiologyNeuronsNociceptionOther FindingPainPathway interactionsPhenotypePhysiologicalPlayPopulationProtein OverexpressionProteinsPublicationsPublishingRecurrent painResearch PersonnelRoleSensorySensory ReceptorsSignal TransductionSkinSkin TemperatureStimulusSynapsesSystemTRPV channelTRPV1 geneTaste PerceptionTemperatureTemperature SenseTestingThermal HyperalgesiasThinkingTissuesTouch sensationTransgenic MiceVisionWorkbasedesignfemoral nervein vivokeratinocytepreferencepromoterreceptorresearch studyresponsetoolwarm temperature
中文摘要
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英文摘要
Recent years have seen great advances in the molecular description of sensory neurobiology. Of the five popularly characterized senses - sight, hearing, taste, smeli, and touch - touch is among the most varied and perhaps least understood. Within this modality is the ability to sense
mechanical forces, chemical stimuli, and temperature, and the molecules that mediate this ability
have been a long-standing mystery. My group and others have recently discovered ion channels
that are activated by different thresholds of temperature, and might enable sensory neurons to
convey temperature information. Among these ion channels is TRPV3, which senses warm
temperatures and is expressed in the skin. Here we use genetic and biochemical tools to test if
TRPV3 and its close homologs play an essential role in thermosensation and pain.
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海外基金