Investigation of calcium signaling in Caenorhabditis elegans

秀丽隐杆线虫钙信号传导的研究

• 批准号: 8505496
• 负责人: Kenneth R Norman
• 金额: $ 29.43万
• 依托单位: ALBANY MEDICAL COLLEGE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8505496
• 关键词: Affect; Aging; Apoptosis; B-Lymphocytes; Behavior; Behavioral; Biological; Biological Assay; Caenorhabditis elegans; Calcium; Calcium Oscillations; Calcium Signaling; Cell Death; Cell Proliferation; Cell division; Cell physiology; Cells; Cellular biology; Complement; Defecation; Family; Family member; Fertilization; Gene Family; Genes; Genetic; Genetic Transcription; Genome; Goals; Guanine Nucleotide Exchange Factors; Guanosine Triphosphate Phosphohydrolases; Heart Diseases; Homologous Gene; Image; Immune system; Invertebrates; Investigation; Knock-out; Lead; Learning; Mammals; Maps; Measures; Mediating; Memory; Metabolism; Methods; Molecular; Molecular Biology; Molecular Genetics; Muscle Contraction; Muscular Dystrophies; Mutation; Myocardium; Necrosis; Neurodegenerative Disorders; Optics; Organelles; Ovulation; Pathway interactions; Phenotype; Preparation; Process; Proteins; Pump; RNA Interference; Regulation; Regulatory Pathway; Reporting; Research; Role; Series; Signal Pathway; Signal Transduction; Signaling Molecule; Skeletal Muscle; Suppressor Mutations; Synapses; Synaptic Vesicles; System; T-Lymphocyte; Techniques; Testing; excitotoxicity; genome wide association study; genome-wide; in vivo; insight; loss of function; mutant; novel; presenilin; public health relevance; response; rho; secretase

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.

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，钙调节失调会以不同的方式和不同程度地影响细胞。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。