The cytoprotective role of zinc transporters in human lung epithelia

锌转运蛋白在人肺上皮细胞中的细胞保护作用

• 批准号: 7393145
• 负责人: DAREN Lee KNOELL
• 金额: $ 37.5万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-05 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7393145
• 关键词: Acute; Acute Lung Injury; Acute-Phase Reaction; Address; Affect; Apical; Apoptosis; Attention; Biological Assay; Carrier Proteins; Cell Death; Cell Line; Cell Survival; Cell physiology; Cells; Cessation of life; Chronic; Condition; Cytoprotection; Cytoprotective Agent; Cytosol; Dermatitis; Dietary Zinc; Disease; Disease susceptibility; Employee Strikes; Epithelial; Epithelial Cells; Epithelium; Event; Family; Functional disorder; Gene Expression; Genes; Genetic; Genetic Polymorphism; Genotype; Homeostasis; Homologous Gene; Human; Human Cell Line; Individual; Inflammation; Inflammatory; Intervention; Investigation; Laboratories; Lead; Location; Lung; Lung diseases; Mammalian Cell; Measurement; Measures; Mediating; Membrane; Metabolism; Mus; Normal Cell; Pathway interactions; Pharmacologic Substance; Physiological; Play; Regulation; Relative (related person); Reporting; Role; Rupture; Signal Transduction; Small Interfering RNA; Stimulus; Stress; Supplementation; Testing; Time; Tissues; Up-Regulation; Variant; Zinc; absorption; cytokine; gastrointestinal epithelium; genetic variant; innovation; insight; member; prevent; response; solute; uptake; zinc-binding protein

DESCRIPTION (provided by applicant): Epithelial cell apoptosis is a hallmark of acute lung injury in inflammatory lung disease yet little is known about the cause of cell death. To study this we have focused our attention on zinc, a known cytoprotectant essential to mammalian cells. Our laboratory reported remarkable differences in cell viability following modulation of intracellular zinc concentration during inflammatory stress. We discovered that zinc initiates intracellular signaling events that promote cell survival and barrier function during inflammatory stress whereas zinc depletion promotes cell death and tissue dysfunction. To extend these studies we turned our attention to zinc transporter proteins. Zinc regulation is highly evolved in metazoa and is comprised of two major families of zinc transporter proteins. The SLC39A family functions as zinc importers to shuttle dietary zinc into the cell and the SLC30A family acts as a counterbalance by exporting excess zinc outside of the cell. Both families are believed to be indispensable for normal cell function as they maintain cellular zinc content with great precision yet little is known regarding their role during conditions of stress. Since we know that zinc is an indispensable component of the lung epithelium during inflammatory stress we predict that zinc transporters also have an essential role. In prelminary studies we made the striking observation that only the zinc importer SLC39A8 was consistently and highly up-regulated, establishing it as a lead candidate responsible for intracellular zinc mobilization into the lung epithelium during inflammatory stress. In this investigation we will test the central hypothesis that modulation of zinc transporter expression and function during inflammatory stress is required for zinc transport sufficient for cell protection against death-inducing stimuli. To do this we will address four specific aims: Specific Aim 1: The role of zinc transporters in human lung epithelium during acute inflammatory stress. Specific Aim 2: SLC39A8 directs zinc into the lung epithelium in response to inflammation leading to cytoprotection. Specific Aim 3: The physiologic consequences of zinc in lung epithelium, and Specific Aim 4: Inter-individual polymorphic variation of zinc transporters as a factor in lung epithelial cell dysfunction and disease. The relevance of this proposal is that it will evaluate an important gap in our current understanding of zinc metabolism, reveal new insight into lung disease susceptibility, and potentially generate innovative strategies to prevent acute lung injury.

描述（由申请人提供）：上皮细胞凋亡是炎性肺病急性肺损伤的标志，但对细胞死亡的原因知之甚少。为了研究这一点，我们把注意力集中在锌，一种已知的哺乳动物细胞所必需的细胞保护剂。我们的实验室报告了炎症应激期间调节细胞内锌浓度后细胞活力的显着差异。我们发现，锌启动细胞内信号传导事件，促进细胞存活和屏障功能在炎症应激，而锌耗竭促进细胞死亡和组织功能障碍。为了扩展这些研究，我们将注意力转向锌转运蛋白。锌的调节在后生动物中高度进化，并且由两个主要的锌转运蛋白家族组成。SLC39A家族作为锌进口商的功能，将膳食锌运送到细胞中，而SLC30A家族通过将过量的锌输出到细胞外而起到平衡作用。这两个家族都被认为是正常细胞功能不可或缺的，因为它们非常精确地维持细胞锌含量，但关于它们在应激条件下的作用知之甚少。由于我们知道锌是炎症应激过程中肺上皮不可或缺的组成部分，我们预测锌转运蛋白也具有重要作用。在初步研究中，我们进行了惊人的观察，只有锌输入者SLC 39A8是一致和高度上调的，确定它是负责炎症应激期间细胞内锌动员到肺上皮中的主要候选者。在这项研究中，我们将测试的中心假设，即在炎症应激过程中的锌转运蛋白的表达和功能的调制是需要足够的锌运输细胞保护对死亡诱导的刺激。为了做到这一点，我们将解决四个具体目标：具体目标1：锌转运蛋白在人类肺上皮细胞在急性炎症应激过程中的作用。具体目标2：SLC39A8引导锌进入肺上皮以响应炎症，从而导致细胞保护。具体目标3：锌在肺上皮中的生理后果，以及具体目标4：锌转运蛋白的个体间多态性变异作为肺上皮细胞功能障碍和疾病的一个因素。该提案的相关性在于，它将评估我们目前对锌代谢的理解中的一个重要空白，揭示对肺部疾病易感性的新见解，并可能产生预防急性肺损伤的创新策略。