Electrophysiological basis of sour taste transduction
Electrophysiological basis of sour taste transduction
批准号:
8652070
负责人:
EMILY R. LIMAN
金额:
$34.93万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-04-01 至 2019-03-31
关键词:
AcidsAction PotentialsAddressCell membraneCellsCytosolDataDetectionElectrodesEpitheliumEventFeeding behaviorsFigs - dietaryFoodGene Expression ProfileHealthHormonesHumanIon ChannelLabelLaboratoriesMediatingMembraneModelingMolecularMusNeuronsNeurotransmitter ReceptorNeurotransmittersNutritionalOrganismPalatePersonal SatisfactionPotassium ChannelProcessProteinsProtonsReceptor ActivationReceptor CellReceptor SignalingRestSafetySensorySensory ReceptorsSignal PathwaySignal TransductionSuctionSystemTRPM5 geneTaste BudsTaste PerceptionTestingTongueTransgenic MiceWorkbasebiophysical propertiescell typeextracellularinsightneurotransmitter releasenovelnovel strategiespatch clamppromoterpublic health relevancereceptorreceptor couplingresearch studyresponsesweet taste perceptiontranscriptome sequencingvoltage
中文摘要
描述(由申请人提供):大多数脊椎动物物种对五种基本味道有反应:甜、苦、鲜、酸和咸,每种味道都提供了关于摄入食物的营养成分和安全性的独特信息。五种味觉品质中的每一种都是由舌头和腭上皮上的味蕾中发现的不同的味觉受体细胞亚群检测的。虽然在理解介导苦味、甜味和鲜味的分子和机制方面取得了很大进展,但对酸味的电生理学基础知之甚少。检测酸味的细胞可以通过TRP离子通道PKD2L1的表达来鉴定,而PKD2L1本身对于酸味是不必要的。在最近的工作中,使用的小鼠,其中黄色荧光蛋白(YFP)是由Pkd2l1的启动子驱动,我们表明,酸味细胞具有以前未表征的质子电导是位于顶部,并携带一个内向电流响应细胞外酸化。这使我们提出了一个模型,其中质子通过质子通道进入细胞去极化,导致动作电位和递质释放。此外,质子进入可引起胞质酸化,其可作用于静息K+通道以进一步使细胞去质子化。该过程可以在多个步骤中进行调节,从而允许系统适应生物体的不同条件和需求。目前的建议包括三个具体的目标,利用这些新产生的转基因小鼠品系和最近的结果,从转录组分析,以测试这个模型,并进一步阐明酸转导的机制。味觉是人类和其他生物调节其摄食行为的重要方式,因此味觉信号传导机制的识别可以对人类健康和福祉产生直接影响。
英文摘要
DESCRIPTION (provided by applicant): Most vertebrate species are responsive to five basic tastes: sweet, bitter, umami, sour and salty, each of which provides unique information on the nutritional content and safety of ingested food. Each of the five taste qualities is detected by a distinct subset of taste receptor cells found in taste buds on the tongue and the palate epithelium. While great strides have been made in understanding the molecules and mechanisms that mediate bitter, sweet, and umami tastes, relatively little is known about the electrophysiological basis for sour taste. The cells that detect sour taste can be identified by expression of the TRP ion channel PKD2L1, which itself is not necessary for sour taste. In recent work, using a mouse in which yellow fluorescent protein (YFP) was driven by the promoter of Pkd2l1, we showed that sour taste cells have a previously uncharacterized proton conductance which is apically located and carries an inward current in response to extracellular acidification. This has led us to propose a model in which proton entry through the proton channel depolarizes the cells leading to action potentials and transmitter release. In addition, proton entry may cause cytosolic acidification, which could act on resting K+ channels to further depolarize the cells. This process may be subject to modulation at multiple steps, allowing the system to adapt to varying conditions and needs of the organism. The present proposal include three specific aims that take advantage of these newly generated transgenic mouse lines and recent results from transcriptome profiling to test this model and to further elucidate mechanisms of sour transduction. Taste is an essential way in which humans and other organisms regulate their ingestive behavior and the identification of mechanisms of taste signaling can therefore have a direct impact on human health and well-being.
期刊论文(0)
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Transcriptome profiling of sour taste cells
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资助金额:$24.6万
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财政年份:2012
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Transcriptome profiling of sour taste cells
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依托单位:
Sensory Transduction in the Vomeronasal System
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Sensory Transduction in the Vomeronasal System
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MOLECULAR MECHANISMS OF VOMERONASAL SENSORY TRANSDUCTION
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海外基金