Function of Omi/HtrA2 in Renal Tubular Cell Death

Omi/HtrA2 在肾小管细胞死亡中的作用

• 批准号: 7535004
• 负责人: ANTONIS S ZERVOS
• 金额: $ 26.64万
• 依托单位: UNIVERSITY OF CENTRAL FLORIDA
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-03-01 至 2010-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7535004
• 关键词: Acute Kidney Failure; Animal Model; Animals; Apoptosis; Apoptotic; Area; Biological Models; Caspase; Cell Death; Cell Survival; Cells; Cessation of life; Chemicals; Cisplatin; Cleaved cell; Cytoplasm; Data; Epithelial Cells; Event; Excision; Grant; Induction of Apoptosis; Injury; Intervention; Ischemia; Kidney; Laboratories; Lead; Mediating; Medical; Mitochondria; Mitochondrial Proteins; Molecular; Mus; Nature; Necrosis; PKD2 protein; Pathway interactions; Patients; Peptide Hydrolases; Physiological; Play; Process; Proteins; Proximal Kidney Tubules; Regulation; Renal function; Reperfusion Therapy; Reporting; Role; Severities; Structure; Testing; Tubular formation; Up-Regulation; Work; antimycin; base; inhibitor/antagonist; injured; kidney cell; mortality; novel; novel strategies; outcome forecast; presenilin-1; prevent; protein protein interaction; renal ischemia; research study

DESCRIPTION (provided by applicant): Acute renal failure (ARF) is a serious medical problem that occurs in 5% of all hospitalized patients. The prognosis of ARF is poor and has remained unchanged over the past three decades carrying a high mortality rate of about 50%. Although ARF is the result of many causes, the most common cause is injury to the renal tubular epithelial cells (RTEC). These cells, once injured, die by necrosis or apoptosis depending on the nature and severity of the insult. Severe injury usually triggers necrosis whereas milder insults to the kidney cause apoptotic death of the RTEC. Necrosis is difficult to prevent, whereas apoptosis can potentially be modulated to maintain cell viability. Therefore, identifying the different components of the apoptotic pathway, especially the ones that play a major role in kidney, can help us understand renal injury-induced apoptosis. These new components can also provide specific and novel targets for intervention to help patients with acute renal failure. Our studies are focused on a recently isolated and characterized pro-apoptotic protease Omi, also known as HtrA2, and its role in renal injury. This protein is present in the mitochondria and is released to the cytoplasm upon induction of apoptosis. In this capacity, Omi is unique both in its structure as well as its function. In the cytoplasm, Omi can induce apoptosis through a caspase-dependent as well as in a caspase-independent pathway. It is the aim of this proposal to investigate the potential role of Omi in the apoptotic cell death that occurs in RTEC. Our studies will investigate the involvement of Omi in renal injury and the molecular events that follow its activation leading to apoptosis. Furthermore, by blocking the proteolytic activity of Omi using a specific inhibitor, a new approach to potentially protect and maintain cell viability will be tested.

描述（由申请人提供）：急性肾衰竭（ARF）是一种严重的医学问题，发生在5%的住院患者中。ARF的预后很差，在过去的三十年里一直保持不变，死亡率约为50%。虽然ARF是许多原因的结果，但最常见的原因是肾小管上皮细胞（RTEC）的损伤。这些细胞一旦受损，根据损伤的性质和严重程度通过坏死或凋亡而死亡。严重的损伤通常引发坏死，而对肾脏的轻度损伤导致RTEC的凋亡性死亡。坏死是难以预防的，而凋亡可以潜在地被调节以维持细胞活力。因此，鉴定凋亡途径的不同组分，特别是在肾脏中起主要作用的组分，可以帮助我们理解肾损伤诱导的细胞凋亡。这些新成分还可以提供特异性和新颖的干预靶点，以帮助急性肾衰竭患者。我们的研究集中在最近分离和表征的促凋亡蛋白酶Omi，也称为HtrA2，及其在肾损伤中的作用。这种蛋白存在于线粒体中，并在诱导细胞凋亡时释放到细胞质中。在这方面，Omi在结构和功能上都是独一无二的。在细胞质中，Omi可以通过半胱天冬酶依赖性以及半胱天冬酶非依赖性途径诱导细胞凋亡。这是这个建议的目的是调查的潜在作用Omi的细胞凋亡中发生的RTEC。我们的研究将探讨Omi在肾损伤中的参与及其激活后导致细胞凋亡的分子事件。此外，通过使用特异性抑制剂阻断Omi的蛋白水解活性，将测试潜在保护和维持细胞活力的新方法。

项目成果

Random mutagenesis of PDZ(Omi) domain and selection of mutants that specifically bind the Myc proto-oncogene and induce apoptosis.

PDZ(Omi)结构域的随机诱变以及特异性结合Myc原癌基因并诱导细胞凋亡的突变体的选择。

• DOI: 10.1038/sj.onc.1206359
• 发表时间: 2003
• 期刊: Oncogene
• 影响因子: 8
• 作者: Junqueira,Daniela;Cilenti,Lucia;Musumeci,Lucia;Sedivy,JohnM;Zervos,AntonisS
• 通讯作者: Zervos,AntonisS

THAP5 is a DNA-binding transcriptional repressor that is regulated in melanoma cells during DNA damage-induced cell death.

THAP5是一种DNA结合的转录阻遏物，在DNA损伤诱导的细胞死亡过程中，在黑色素瘤细胞中受调节。

• DOI: 10.1016/j.bbrc.2010.11.092
• 发表时间: 2011-01-07
• 期刊: Biochemical and biophysical research communications
• 影响因子: 3.1
• 作者: Balakrishnan MP;Cilenti L;Ambivero C;Goto Y;Takata M;Turkson J;Li XS;Zervos AS
• 通讯作者: Zervos AS

Regulation of Abro1/KIAA0157 during myocardial infarction and cell death reveals a novel cardioprotective mechanism for Lys63-specific deubiquitination.

• DOI: 10.1016/j.yjmcc.2010.12.015
• 发表时间: 2011-04
• 期刊: Journal of molecular and cellular cardiology
• 影响因子: 5
• 作者: Cilenti L;Balakrishnan MP;Wang XL;Ambivero C;Sterlicchi M;del Monte F;Ma XL;Zervos AS
• 通讯作者: Zervos AS