Investigation of calcium signaling in Caenorhabditis elegans
Investigation of calcium signaling in Caenorhabditis elegans
批准号:
8096801
负责人:
Kenneth R Norman
金额:
$30.5万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-01 至 2015-06-30
关键词:
AffectAgingApoptosisB-LymphocytesBehaviorBehavioralBiologicalBiological AssayCaenorhabditis elegansCalciumCalcium OscillationsCalcium SignalingCell DeathCell ProliferationCell divisionCell physiologyCellsCellular biologyComplementDefecationFamilyFamily memberFertilizationGene FamilyGenesGeneticGenetic TranscriptionGenomeGoalsGuanine Nucleotide Exchange FactorsGuanosine Triphosphate PhosphohydrolasesHeart DiseasesHomologous GeneImageImmune systemInvertebratesInvestigationKnock-outLeadLearningMammalsMapsMeasuresMediatingMemoryMetabolismMethodsMolecularMolecular BiologyMolecular GeneticsMuscle ContractionMuscular DystrophiesMutationMyocardiumNecrosisNeurodegenerative DisordersOpticsOrganellesOvulationPathway interactionsPhenotypePreparationProcessProteinsPumpRNA InterferenceRegulationRegulatory PathwayReportingResearchRoleSeriesSignal PathwaySignal TransductionSignaling MoleculeSkeletal MuscleSuppressor MutationsSynapsesSynaptic VesiclesSystemT-LymphocyteTechniquesTestingexcitotoxicitygenome wide association studygenome-widein vivoinsightloss of functionmutantnovelpresenilinpublic health relevanceresponserhosecretase
中文摘要
描述(由申请人提供):包括肌肉收缩、转录、细胞分裂和突触囊泡释放的总结。特别地,钙也可以触发细胞死亡和细胞坏死。因此,钙调节的失调可以以不同的方式和不同的程度影响细胞。因此,钙的水平需要严格控制。事实上,钙信号传导缺陷与许多神经退行性疾病、肌肉萎缩症和心脏病有关。为了了解钙信号的调节,我们建立了一个新的系统来鉴定参与调节和响应细胞溶质钙水平的基因产物。此外,我们还开发了一种新的制剂来测量体内钙动力学。以前,我们发现,VAV-1,一个高度进化保守的鸟嘌呤核苷酸交换因子的Rho家族GTP酶,调节几个节奏的行为,在秀丽隐杆线虫通过调节钙振荡。这些节律性行为包括咽部泵血、排卵和受精以及排便。为了理解VAV-1调节钙振荡和这些节律行为的机制,我们使用了C. elegans遗传学,以确定其他潜在的钙调节剂。到目前为止,我们的分析已经发现了VAV-1调节细胞内钙储存的释放以调节细胞溶质钙水平的证据。为了阐明VAV-1控制钙信号和节律行为的机制,我们正在采取多方面的方法,包括体内钙成像与遗传学,分子和细胞生物学技术相结合,以探索VAV-1依赖的钙信号调节。由于脊椎动物和无脊椎动物的信号级联之间有许多相似之处,证据表明它们在分子,结构和功能水平上具有共性,因此本提案的目标将有助于理解钙信号转导中涉及的体内机制。
公共卫生相关性:钙信号的调节在许多领域都是至关重要的,包括心肌和骨骼肌收缩、突触活动、学习和记忆、兴奋性毒性和细胞坏死以及衰老。我们的长期目标是利用遗传、分子和细胞生物学方法来解决细胞用于调节和破译钙信号的机制。
英文摘要
DESCRIPTION (provided by applicant): Summary including muscle contraction, transcription, cell division, and synaptic vesicle release. Paradoxically, calcium can also trigger cell death and cellular necrosis. Therefore, dysregulation in calcium regulation can affect cells in different ways and to varying degrees. Consequently, the levels of calcium need to be tightly regulated. Indeed, defective calcium signaling has been implicated in many neurodegenerative diseases, muscular dystrophies and heart disease. To understand the regulation of calcium signaling, we have established a novel system to identify gene products involved in the regulation and response to cytosolic calcium levels. Furthermore, we have developed a novel preparation to measure calcium dynamics in vivo. Previously, we found that VAV-1, a highly evolutionarily conserved guanine nucleotide exchange factor for the Rho Family GTPases, regulates several rhythmic behaviors in Caenorhabditis elegans by modulating calcium oscillations. These rhythmic behaviors include pharyngeal pumping, ovulation and fertilization, and defecation. To understand the mechanism(s) VAV-1 utilizes to regulate calcium oscillations and these rhythmic behaviors, we have used the power of C. elegans genetics to identify other potential regulators of calcium. Our analyses thus far have found evidence that VAV-1 modulates the release of calcium from intracellular stores to regulate cytosolic calcium levels. In order to elucidate the mechanisms underlying VAV-1's control of calcium signaling and rhythmic behavior, we are taking a multifaceted approach, which involves in vivo calcium imaging in concert with genetic, molecular and cell biology techniques to explore VAV-1 dependent regulation of calcium signaling. Since there are many similarities between vertebrate and invertebrate signaling cascades and evidence points to their commonality at the molecular, structural and functional level, the goals of this proposal will aid in understanding the in vivo mechanisms involved in calcium signaling.
PUBLIC HEALTH RELEVANCE: The regulation of calcium signaling is of paramount importance to many fields, including cardiac and skeletal muscle contraction, synaptic activity, learning and memory, excitotoxicity and cellular necrosis, and aging. Our long-term goals are to resolve the mechanisms that cells use to regulate and decipher calcium signaling using genetic, molecular and cell biological methods.
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会议论文
Deciphering Molecular Mechanisms of Calcium Homeostasis
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批准号:10796459
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项目类别:
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资助金额:$18.47万
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财政年份:2022
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负责人:Kenneth R Norman
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依托单位:
Deciphering Molecular Mechanisms of Calcium Homeostasis
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批准号:10406433
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项目类别:
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资助金额:$40.75万
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财政年份:2022
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负责人:Kenneth R Norman
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依托单位:
Investigating the Molecular Mechanisms of Mitochondrial Calcium Uptake in Caenorhabditis elegans
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批准号:10286974
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项目类别:
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资助金额:$20.38万
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财政年份:2021
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负责人:Kenneth R Norman
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依托单位:
Investigating the Molecular Mechanisms of Mitochondrial Calcium Uptake in Caenorhabditis elegans
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批准号:10456980
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项目类别:
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资助金额:$24.45万
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财政年份:2021
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负责人:Kenneth R Norman
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Investigation of calcium signaling in Caenorhabditis elegans
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批准号:8291070
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项目类别:
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资助金额:$30.5万
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财政年份:2010
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负责人:Kenneth R Norman
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Investigation of calcium signaling in Caenorhabditis elegans
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批准号:8683191
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项目类别:
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资助金额:$30.5万
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财政年份:2010
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负责人:Kenneth R Norman
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Investigation of Calcium Signaling in Caenorhabditis elegans
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批准号:9893416
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项目类别:
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资助金额:$6.69万
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Investigation of Calcium Signaling in Caenorhabditis elegans
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批准号:9353426
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项目类别:
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资助金额:$31.6万
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财政年份:2010
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负责人:Kenneth R Norman
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依托单位:
Investigation of calcium signaling in Caenorhabditis elegans
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批准号:7993387
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项目类别:
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资助金额:$29.22万
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财政年份:2010
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负责人:Kenneth R Norman
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依托单位:
Investigation of calcium signaling in Caenorhabditis elegans
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批准号:8505496
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项目类别:
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资助金额:$29.43万
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财政年份:2010
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负责人:Kenneth R Norman
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依托单位:
海外基金