Molecular, Genetic & Physiological Studies of Calcium-activated Chloride Channels

分子、遗传

• 批准号: 8489363
• 负责人: LILY Y JAN
• 金额: $ 29.28万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-07-15 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8489363
• 关键词: Action Potentials; Affect; Afferent Neurons; Ambystoma; Axotomy; Binding; Biochemical; Bioinformatics; Calcium; Calmodulin; Cell physiology; Chloride Channels; Cohort Studies; Collaborations; Complement; Complex; Cystic Fibrosis; Denervation; Diabetes Mellitus; Disease; Dominant-Negative Mutation; Epithelial Cells; Exocrine Glands; Family; Feedback; Future; Generations; Green Algae; Herpes zoster disease; Hypertension; Injection of therapeutic agent; Integral Membrane Protein; Interleukin-4; Ion Channel; Knock-out; Knockout Mice; Knowledge; Malignant Neoplasms; Mammals; Mechanics; Messenger RNA; Microarray Analysis; Microscopy; Mind; Molecular; Molecular Genetics; Mus; Mutagenesis; Mutation; Nerve Regeneration; Neurons; Nociception; Oocytes; Organism; Pain; Pattern; Peptides; Peripheral; Peripheral Nervous System; Physiological; Potassium Channel; Property; Protons; Publishing; Regulation; Reporting; Role; Sensory; Signal Transduction; Spinal Ganglia; System; Testing; Time; Transcript; Up-Regulation; Work; Xenopus; Xenopus oocyte; airway epithelium; allodynia; chemotherapy; computerized data processing; design; expression cloning; interest; mutant; nerve injury; novel; painful neuropathy; postnatal; prevent; research study; response; sciatic nerve lesion; single molecule; stoichiometry; therapeutic target; trafficking; voltage

DESCRIPTION (provided by applicant): Calcium-activated chloride channels (CaCCs) serve important physiological functions including modulation of signal processing of a variety of central and peripheral neurons. For example, CaCC contributes to signal amplification of sensory inputs and regulation of excitability of both sensory and central neurons. The long- term objectives are to understand how these channels work, and how they regulate neuronal activity. Reflecting an intense interest in CaCCs as potential therapeutic targets for hypertension, cystic fibrosis and other diseases, there have been extensive efforts to determine the molecular identity of CaCCs. Because the channel properties and expression patterns of several reported molecular candidates do not match those for native CaCCs, several years ago we began the undertaking for expression cloning, leading to the identification of Xenopus and mouse TMEM16A, as well as mouse TMEM16B as CaCC subunits. In 2008, two concurrent studies were published around the same time as ours, and all three reached the same conclusion that mammalian TMEM16A corresponds to CaCC. By now, several studies of TMEM16A knockout mice have shown that TMEM16A is required for CaCC in exocrine glands and airway epithelia. With the TMEM16 family of "transmembrane proteins with unknown function" emerging as a novel family of ion channels, even the most basic questions are open and now amenable to molecular and genetic studies: How does calcium activate CaCC? How many TMEM16A subunits are present in a CaCC channel? Does TMEM16A correspond to the CaCC in sensory neurons of the dorsal root ganglion (DRG)? Is TMEM16A up regulated following denervation and, if so, does it influence nerve regeneration and/or neuropathic pain? Denervation causes up regulation of CaCC of DRG neurons - one of the best examples of neuronal CaCC, hence one specific aim of this proposal is to examine the involvement of TMEM16A in CaCC of DRG neurons with or without sciatic nerve lesion, and to explore potential roles of TMEM16A in pain sensitivity and neuropathic pain, which develops after nerve injury or in diseases like diabetes, herpes, and cancer. To better understand how CaCC channel traffic and activity may be controlled by cytosolic calcium, we will carry out biochemical and mutagenesis studies of TMEM16A, which can be heterogeneously expressed to generate CaCC. We will also use a combination of approaches to determine the CaCC stoichiometry - an important question for better appreciation of CaCC function and regulation, and the diversity of CaCCs.

描述（由申请人提供）：钙活化的氯离子通道（CaCCs）具有重要的生理功能，包括调节各种中枢和外周神经元的信号处理。例如，CaCC参与了感觉输入的信号放大和感觉神经元和中枢神经元兴奋性的调节。长期目标是了解这些通道是如何工作的，以及它们是如何调节神经元活动的。作为高血压、囊性纤维化和其他疾病的潜在治疗靶点，人们对CaCCs的分子特性进行了广泛的研究，这反映了人们对CaCCs的浓厚兴趣。由于一些报道的候选分子的通道特性和表达模式与天然CaCC不匹配，几年前我们开始了表达克隆的工作，最终鉴定出爪虫和小鼠TMEM16A，以及小鼠TMEM16B作为CaCC亚基。2008年，有两项研究与我们的研究同时发表，这三项研究都得出了相同的结论，即哺乳动物TMEM16A与CaCC相对应。目前，几项TMEM16A敲除小鼠的研究表明，外分泌腺和气道上皮的CaCC需要TMEM16A。随着TMEM16“功能未知的跨膜蛋白”家族作为一种新的离子通道家族的出现，即使是最基本的问题也是开放的，现在可以进行分子和遗传学研究：钙是如何激活CaCC的？在一个CaCC信道中有多少TMEM16A亚基？TMEM16A是否与背根神经节（DRG）感觉神经元中的CaCC相对应？TMEM16A在去神经支配后是否上调，如果是，它是否影响神经再生和/或神经性疼痛？去神经支配导致DRG神经元CaCC的上调，这是神经元CaCC的最佳例子之一，因此本研究的一个具体目的是研究TMEM16A在有或没有坐骨神经损伤的DRG神经元CaCC中的参与，并探讨TMEM16A在疼痛敏感性和神经性疼痛中的潜在作用，这些疼痛是在神经损伤后或在糖尿病、疱疹和癌症等疾病中发生的。为了更好地了解细胞质钙如何控制CaCC通道的流量和活性，我们将对TMEM16A进行生化和诱变研究，TMEM16A可以异质表达产生CaCC。我们还将使用多种方法来确定CaCC的化学计量学，这是更好地了解CaCC功能和调控以及CaCC多样性的一个重要问题。