Regulation of capacitative calcium entry in porcine oocytes

猪卵母细胞电容性钙进入的调节

• 批准号: 7293364
• 负责人: ZOLTAN MACHATY
• 金额: $ 7.29万
• 依托单位: PURDUE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-23 至 2009-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7293364
• 关键词: Animals; Binding; Biological Assay; Biomedical Research; Calcium; Calcium Signaling; Cell membrane; Cytosol; Data; Development; Disease; Double-Stranded RNA; Down-Regulation; Endoplasmic Reticulum; Eukaryotic Cell; Family suidae; Fertilization; Gene Expression; Gene Targeting; Generations; Genetic; Goals; Hela Cells; Homologous Gene; Label; Livestock; Mammals; Mediating; Methods; Modeling; Modification; Monitor; Mutation; Numbers; Oocytes; Pathway interactions; Personal Satisfaction; Pharmacologic Substance; Procedures; Production; Proteins; Purpose; RNA Interference; Regulation; Research; Reverse Transcriptase Polymerase Chain Reaction; Role; STIM1 gene; Signal Transduction; Signal Transduction Pathway; Somatic Cell; Sus scrofa; System; T-Lymphocyte; Techniques; Technology; Therapeutic Intervention; Transgenic Animals; Transgenic Organisms; base; citrate carrier; design; extracellular; human STIM1 protein; human disease; improved; member; novel; nuclear transfer; oocyte maturation; programs; protein function; research study; sensor; sperm cell

DESCRIPTION (provided by applicant): During fertilization in mammals, the sperm utilizes repetitive calcium signals to activate the oocyte's developmental program. The fertilizing sperm triggers a release of calcium from the intracellular stores that is followed by a calcium influx through channels in the oocyte plasma membrane. Although a calcium influx generated by store depletion is vital for the generation of the long-lasting signal, the mechanisms that regulate this capacitative calcium entry are largely unknown. The overall goal of the proposal is to define the regulatory mechanisms of capacitative calcium entry in porcine oocytes. Our aim is to investigate the role of STIM1 in capacitative calcium entry. In somatic cells, STIM1 has been suggested to serve as a calcium sensor to detect calcium levels in the intracellular stores and in preliminary experiments we demonstrated that porcine oocytes also express a STIM1 homolog. Here we propose to determine the dynamics of STIM1 gene expression during oocyte maturation by means of quantitative RT-PCR. By using a fluorescently labeled probe, STIM1 will be shown to translocate from the cytosol to the plasma membrane after store depletion and data will be presented that downregulation of its function with siRNAs inhibits capacitative calcium entry. The information obtained through the proposed experiments will help in the development of novel oocyte activation methods that will increase the efficiency of nuclear transfer technology. This is believed to be critical for the large scale production of transgenic large animals. Such animals with specific genetic modifications are regarded as extremely valuable models for a great number of human diseases: they help to better understand disease mechanisms and also, to develop new strategies for therapeutic interventions. The information obtained through the proposed experiments will contribute to the effective production of transgenic large animals to be used as models for human diseases. By using the animals with specific genetic alterations it will be possible to better understand the mechanism of diseases and develop new and effective therapies.

描述（由申请人提供）：在哺乳动物的受精过程中，精子利用重复的钙信号来激活卵母细胞的发育程序。受精卵触发细胞内钙库释放钙，随后钙通过卵母细胞质膜的通道流入。虽然钙池耗竭产生的钙内流是产生持久信号的关键，但调节这种容量性钙内流的机制在很大程度上是未知的。该提案的总体目标是确定在猪卵母细胞的能力钙进入的调节机制。我们的目的是研究STIM 1在容量性钙内流中的作用。在体细胞中，STIM 1已被建议作为钙传感器，以检测细胞内的钙水平存储和在初步实验中，我们证明，猪卵母细胞也表达一个STIM 1同源。在这里，我们建议通过定量RT-PCR来确定在卵母细胞成熟过程中STIM 1基因表达的动态。通过使用荧光标记的探针，STIM 1将被证明从细胞质易位到质膜后存储耗尽和数据将呈现，下调其功能与siRNA抑制容量钙离子进入。通过拟议的实验获得的信息将有助于开发新的卵母细胞激活方法，提高核移植技术的效率。这被认为是大规模生产转基因大型动物的关键。这些具有特定遗传修饰的动物被认为是许多人类疾病的极有价值的模型：它们有助于更好地了解疾病机制，并制定新的治疗干预策略。通过拟议的实验获得的信息将有助于有效生产转基因大型动物，用作人类疾病的模型。通过使用具有特定遗传改变的动物，将有可能更好地了解疾病的机制并开发新的有效疗法。