Molecular Mechanisms Controlling Homeostatic Cellular Excitability
Molecular Mechanisms Controlling Homeostatic Cellular Excitability
批准号:
8774258
负责人:
Tingting Wang
金额:
$6.0万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-12-01 至 2015-11-30
关键词:
AffectBiological AssayBiologyCalciumCell physiologyCellsCollagenDataDevelopmentDiseaseDrosophila genusElectrophysiology (science)EpilepsyExhibitsExtracellular DomainExtracellular MatrixExtracellular Matrix ProteinsGenesGenetic ScreeningGenetic screening methodHeart RateHomeostasisHomologous GeneHumanKnowledgeLaboratoriesMigraineMolecularMorphologyMuscleMutationMyocardiumN-terminalNerveNervous system structureNeuronsOrganismOutputPhysiologicalPhysiologyPopulationProcessPropertyProteinsRegulationSeveritiesSignal TransductionSignaling MoleculeStructureSynapsesSynaptic TransmissionSynaptic plasticitySystemWorkbaseblood glucose regulationblood pressure regulationbrain cellchemical geneticsflymutantnervous system disorderneuromuscularneurotransmitter releasepostsynapticpresynapticreceptor functionrelating to nervous systemresearch studysynaptogenesistransmission processvesicular releasevoltage
中文摘要
描述(申请人提供):动态平衡信号系统在整个生物学中无处不在。根据定义,动态平衡是指细胞或细胞系统对扰动做出反应并保持恒定生理的能力。这一概念已被应用于血压和心率的系统水平控制以及细胞生理系统,包括葡萄糖和细胞内钙的控制4。现在很明显,进化上保守的动态平衡信号系统已经进化到稳定神经和肌肉的兴奋性4。尽管假设控制细胞兴奋的动态平衡信号系统很重要,但人们对其潜在的分子机制知之甚少。在一项大规模的正向遗传筛查中,戴维斯实验室发现了果蝇多重蛋白(DMP)基因的突变,该基因编码一种细胞外基质蛋白,可阻止突触传递的动态平衡调节,称为突触动态平衡。有趣的是,这种细胞外基质蛋白在发育过程中专门调节突触的动态平衡,而不改变突触的形态。因此,它可能作为逆行信号分子,在突触后受体功能受扰时调节突触前神经递质的释放。研究DMP基因的功能将极大地促进我们对突触内稳态的分子机制的了解,这是一个进化上保守的过程,发生在从果蝇到人类的各种生物的NMJ。重要的是,DMP基因具有脊椎动物的同源物,在心肌和神经系统29中表达,潜在地发挥保守的功能,维持神经和肌肉的适当的兴奋性。因此,解开细胞外基质蛋白在突触传递和动态平衡可塑性中的功能,
是开发胶原蛋白相关神经疾病新疗法的关键一步。
英文摘要
DESCRIPTION (provided by applicant): Homeostatic signaling systems are ubiquitous throughout biology. By definition, homeostasis refers to the ability of a cell or system of cells t respond to a perturbation and maintain a constant physiology. This concept has been applied to the system level control of blood pressure and heart rate as well as cellular physiological systems including control of glucose and intracellular calcium4. It is now apparent that evolutionarily conserved homeostatic signaling systems have evolved to stabilize the excitable properties of nerve and muscle4. Despite the hypothesized importance of the homeostatic signaling systems that control cellular excitation, very little is known about the underlying molecular mechanisms. In a large-scale forward genetic screen the Davis laboratory has identified mutations in the Drosophila multiplexin (dmp) gene, encoding an extracellular matrix protein, that blocks the homeostatic regulation of synaptic transmission, termed 'synaptic homeostasis'. Intriguingly, this extracellular matrix protein specifically regulates synaptic homeostasis without changing synapse morphology during development. Thus, it can potentially function as the retrograde signaling molecule that modulates presynaptic neurotransmitter release upon perturbations of postsynaptic receptor function. Studying the function of the dmp gene would significantly advance our knowledge of the molecular mechanisms of synaptic homeostasis, an evolutionarily conserved process that occurs at the NMJ of organisms ranging from Drosophila to humans. Importantly, the dmp gene has vertebrate homologues that are expressed in cardiac muscles and nervous system29, potentially serving a conserved function to maintain the appropriate excitable properties of nerve and muscle. Unraveling the function of extracellular matrix proteins in synaptic transmission and homeostatic plasticity could, therefore,
be a critical step in developing new treatments for collagen-related neurological diseases.
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专著(0)
科研奖励(0)
会议论文
Retrograde Signaling for Homeostatic Control of Synaptic Transmission
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批准号:10186987
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项目类别:
-
资助金额:$42.28万
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财政年份:2021
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负责人:Tingting Wang
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依托单位:
Stabilizing Brain Function via Glial Epigenetic Signaling
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批准号:10438708
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项目类别:
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资助金额:$34.21万
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财政年份:2020
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负责人:Tingting Wang
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依托单位:
Stabilizing Brain Function via Glial Epigenetic Signaling
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批准号:10656206
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项目类别:
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资助金额:$36.97万
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财政年份:2020
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负责人:Tingting Wang
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依托单位:
Stabilizing Brain Function via Glial Epigenetic Signaling
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批准号:10188664
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项目类别:
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资助金额:$34.02万
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财政年份:2020
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负责人:Tingting Wang
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依托单位:
Stabilizing Brain Function via Glial Epigenetic Signaling
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批准号:10023782
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项目类别:
-
资助金额:$37.61万
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财政年份:2020
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负责人:Tingting Wang
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依托单位:
Molecular Mechanisms Controlling Homeostatic Cellular Excitability
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批准号:8454908
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项目类别:
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资助金额:$5.39万
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财政年份:2012
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负责人:Tingting Wang
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依托单位:
海外基金