Neurobiological Basis for Cold Transduction
Neurobiological Basis for Cold Transduction
批准号:
7848962
负责人:
David D McKemy
金额:
$35.3万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-01 至 2012-06-30
关键词:
AccountingAddressAfferent NeuronsAnimal ModelBehaviorBehavioralBiologicalBiological AssayCapsaicinCellsCutaneousDetectionEsthesiaFamilyGoalsGreen Fluorescent ProteinsHeatingHomeostasisIn VitroInjuryIon ChannelLabelLaboratoriesMammalsMediatingMentholMetabolicModalityModificationMolecularMusNerveNerve FibersNervous system structureNeurobiologyNeurogliaNeuronsNociceptionPainPatternPeripheralPeripheral Nervous SystemPropertyPsychophysiologyReportingResearchRoleSensorySignal TransductionSkinSpinalStimulusTRPV1 geneTemperatureTemperature SenseTestingTissuesTouch sensationTransgenic Micebasecellular transductioncold temperaturedetectorgraspin vivomembermouse modelneurochemistrynovelpromoterprotein expressionreceptorsensorsensory mechanismsomatosensory
中文摘要
描述(由申请人提供):在外周神经系统中,体感神经元报告范围广泛的温度,从有害的热到有害的冷。我们知道,不同的神经纤维子集会对特定的温度阈值做出反应,这可能是基于它们表达的热敏分子。此外,这些神经是检测疼痛、组织损伤刺激的关键参与者。我们最近已经开始掌握这些神经纤维如何检测温度,因为识别了对不同热刺激做出反应的分子。这些分子是瞬时受体电位(TRP)通道家族的成员,通过它们对化合物(如辣椒素和薄荷醇)的敏感性进行鉴定,这些化合物模拟了不同的心理物理感觉。总的来说,这些温度传感器可以检测到我们感知到的广泛的温度范围,并为如何检测温度提供了分子解释。尽管如此,我们对介导和调节这些热敏元件的细胞转导机制的理解仍然有限。因此,我们正在分析表达冷和薄荷醇受体TRPM8的感觉传入,以进一步表征介导冷感觉的转导机制。为此,我们已经产生了转基因小鼠,表达的荧光标记,特异性在TRPM8阳性感觉神经元,是在体内检测。通过这种动物模型,我们正在研究冷敏感传入神经的外周投射,天然细胞中冷适应的机制,以及这些神经元在躯体感觉中的体内作用。
英文摘要
DESCRIPTION (provided by applicant): In the peripheral nervous system, somatosensory neurons report a wide range of temperatures, from noxious heat to noxious cold. We know that distinct subsets of nerve fibers will respond to specific temperature thresholds, presumably based upon the thermosensory molecules they express. Moreover, these nerves are key players in the detection of painful, tissue damaging stimuli. We have recently begun to grasp how these nerve fibers detect temperature due to the identification of molecules that respond to distinct thermal stimuli. These molecules, members of the transient receptor potential (TRP) channel family, were identified by their sensitivity to compounds, such as capsaicin and menthol, which mimic distinct psychophysical sensations. Taken together, these thermosensors can detect the broad range of temperatures we perceive and provides a molecular explanation for how temperature is detected. Nonetheless, our understanding of the cellular transduction mechanisms that mediate and regulate these thermosensors remains limited. Therefore, we are analyzing the sensory afferents expressing the cold and menthol receptor, TRPM8, to further our characterization of the transduction mechanisms mediating cold sensation. To this end, we have generated transgenic mice that express a fluorescent label specifically in TRPM8-positive sensory neurons that is detectable in vivo. With this animal model, we are investigating the peripheral projections of cold-sensitive afferents, the mechanisms of cold adaptation in native cells, and the in vivo role of these neurons in somatosensation.
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会议论文
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财政年份:2014
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财政年份:2012
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Translational profiling of somatosensory afferent neurons
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批准号:8280848
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财政年份:2012
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The role of TRPA1 neurons in inflammatory pain
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财政年份:2011
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依托单位:
The role of TRPA1 neurons in inflammatory pain
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批准号:8242467
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财政年份:2011
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Neurobiological Basis for Cold Transduction
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依托单位:
Neurobiological Basis for Cold Transduction
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项目类别:
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资助金额:$35.66万
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财政年份:2007
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负责人:David D McKemy
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依托单位:
Neurobiological Basis for Cold Transduction
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批准号:7644834
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资助金额:$35.66万
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财政年份:2007
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负责人:David D McKemy
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依托单位:
Genetic Mapping of Somatosensory Neural Networks
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批准号:6907025
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财政年份:2005
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批准号:7010003
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依托单位:
海外基金