Role of Klotho Ectodomain Release in Suppression of Aging

Klotho 胞外域释放在抑制衰老中的作用

• 批准号: 7314627
• 负责人: HUIZHOU FAN
• 金额: $ 6.4万
• 依托单位: UNIV OF MED/DENT NJ-R W JOHNSON MED SCH
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-07-15 至 2009-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7314627
• 关键词: Address; Affect; Age; Aging; Aging-Related Process; Alleles; American; Amino Acids; Animals; Arteriosclerosis; Atrophic condition of skin; Biological; Cell Line; Cell surface; Cells; Cessation of life; Cleaved cell; Cultured Cells; Data; Disease; Endopeptidases; Enzymes; Exhibits; Face; Future; Genes; Goals; Grant; Hand; Human; In Vitro; Integral Membrane Protein; Knockout Mice; Life Expectancy; Life Extension; Lipodystrophy; Longevity; Mass Spectrum Analysis; Mediating; Membrane; Metalloproteases; Mus; Mutate; Mutation; Object Attachment; Osteoporosis; Peptide Hydrolases; Peptides; Plasma; Premature aging syndrome; Prevention; Protein Overexpression; Pulmonary Emphysema; Quality of life; Radioimmunoassay; Research Personnel; Role; Site; Small Interfering RNA; Societies; Testing; Tumor Necrosis Factor-alpha; Tumor Necrosis Factors; Variant; Wild Type Mouse; Work; age group; age related; aging population; anti aging; base; calcification; comparative; expression vector; functional genomics; human TNF protein; improved; in vivo; insight; klotho protein; synthetic peptide; Address; Affect; Age; Aging; Aging-Related Process; Alleles; American; Amino Acids; Animals; Arteriosclerosis; Atrophic condition of skin; Biological; Cell Line; Cell surface; Cells; Cessation of life; Cleaved cell; Cultured Cells; Data; Disease; Endopeptidases; Enzymes; Exhibits; Face; Future; Genes; Goals; Grant; Hand; Human; In Vitro; Integral Membrane Protein; Knockout Mice; Life Expectancy; Life Extension; Lipodystrophy; Longevity; Mass Spectrum Analysis; Mediating; Membrane; Metalloproteases; Mus; Mutate; Mutation; Object Attachment; Osteoporosis; Peptide Hydrolases; Peptides; Plasma; Premature aging syndrome; Prevention; Protein Overexpression; Pulmonary Emphysema; Quality of life; Radioimmunoassay; Research Personnel; Role; Site; Small Interfering RNA; Societies; Testing; Tumor Necrosis Factor-alpha; Tumor Necrosis Factors; Variant; Wild Type Mouse; Work; age group; age related; aging population; anti aging; base; calcification; comparative; expression vector; functional genomics; human TNF protein; improved; in vivo; insight; klotho protein; synthetic peptide

DESCRIPTION (provided by applicant): The life expectancy for Americans has been rising continuously. As a result, society faces challenges of age-related diseases. On the other hand, there are still people who suffer untimely death from premature aging. A better understanding of mechanisms underlying aging and age-related diseases is needed to solve these issues. Mice carrying inactivated klotho gene alleles exhibit hallmarks of human aging, suggesting that the Klotho protein is required for the extension of life and the suppression of age-related diseases. The Klotho protein is biosynthesized as a transmembrane protein whose ectodomain is released at the cell surface. The mechanisms for and the biological significance of Klotho ectodomain release are currently unknown. The long-term goal of this study is to identify the protease responsible for generating soluble Klotho and to determine the role of Klotho ectodomain release in suppression of aging and age-related diseases. Preliminary studies have shown that the Klotho ectodomain is released in cultured cells by the tumor necrosis factor-a converting enzyme (TACE). This work will further determine whether TACE is physiologically responsible for Klotho ectodomain release. This question will be addressed by determining the effect of siRNA-mediated TACE expression knockdown on Klotho release in cultured cells, and by comparing the plasma Klotho levels in TACE-null and wild-type mice using an established Klotho radioimmunoassay. The investigators will also identify the TACE cleavage site in transmembrane Klotho by mass spectrometry. They will confirm the cleavage site by constructing a Klotho variant containing mutations at the cleavage site, and determine if the mutations affect Klotho cleavage in cells and with synthetic peptide substrates. Finally, these researchers will investigate the role of TACE-mediated Klotho release in aging by determining whether the activity of Klotho release in vivo correlates with age. This work will reveal insights into the mechanisms that underlie the anti-aging activity of Klotho. It may identify Klotho release as a target for manipulating Klotho activity, which can be used for lifespan extension, and for the prevention and treatment of age-related diseases.

描述（由申请人提供）：美国人的预期寿命一直在不断上升。结果，社会面临与年龄有关的疾病的挑战。另一方面，仍然有一些人因过早衰老而过时死亡。需要更好地了解衰老和与年龄有关的疾病的机制来解决这些问题。携带失活的Klotho基因等位基因的小鼠具有人类衰老的标志，这表明Klotho蛋白是延长生命和抑制与年龄相关疾病所必需的。 klotho蛋白被生物合成为跨膜蛋白，其子宫骨蛋白在细胞表面释放。目前尚不清楚Klotho外生域释放的机制和生物学意义。这项研究的长期目标是确定负责产生可溶性klotho的蛋白酶，并确定klotho ectodomain释放在抑制衰老和年龄相关疾病中的作用。初步研究表明，肿瘤坏死因子-A转化酶（TACE）在培养细胞中释放了klotho ectodobain。这项工作将进一步确定TACE是否对Klotho外生域的释放负责。通过确定siRNA介导的TACE表达敲低对培养细胞中Klotho释放的影响，以及通过使用已建立的Klotho doadition Notial-Munoassay进行比较的血浆Klotho水平来解决这个问题。研究人员还将通过质谱法鉴定跨膜Klotho中的TACE裂解位点。他们将通过在裂解位点构建包含突变的klotho变体来确认裂解位点，并确定突变是否影响细胞中的klotho裂解和合成肽底物。最后，这些研究人员将通过确定klotho释放在体内的活性是否与年龄相关的活性来研究TACE介导的Klotho释放在衰老中的作用。这项工作将揭示有关克洛托抗衰老活动基础的机制的见解。它可以将Klotho释放视为操纵Klotho活动的目标，可用于延长寿命，并用于预防和治疗与年龄相关的疾病。