Senescence and Autophagy as Mediators of Glomerular Injury in Diabetes

衰老和自噬作为糖尿病肾小球损伤的介质

• 批准号: 8585056
• 负责人: Astrid Weins
• 金额: $ 15.92万
• 依托单位: BRIGHAM AND WOMEN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-02-15 至 2016-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8585056
• 关键词: Adhesions; Adhesiveness; Aging; Albuminuria; Apoptosis; Attenuated; Autophagocytosis; Biopsy; Budgets; Cell Aging; Cell Cycle Arrest; Cell Survival; Cells; Chronic Kidney Failure; Clinical; Coculture Techniques; Collection; Complex; Complication; Development; Diabetes Mellitus; Diabetic Nephropathy; Diagnosis; Dialysis procedure; Disease; Disease Progression; Early treatment; Elements; End stage renal failure; Endothelial Cells; Endothelium; Equilibrium; Extracellular Matrix; Focal Adhesions; Foot Process; Homeostasis; Homologous Gene; Human; Hypertrophy; In Vitro; Injury; Kidney; Kidney Failure; Kidney Glomerulus; Left; Link; Maintenance; Mediating; Mediator of activation protein; Medicare; Metabolic stress; Modeling; Molecular; Mus; Nature; Pathologic; Patients; Phenotype; Prevention therapy; Process; Proteinuria; Renal glomerular disease; Reporting; Role; Signal Transduction; Stress; Testing; Tissues; Transplantation; United States; Up-Regulation; Validation; Work; autocrine; base; cell injury; cell type; diabetic; glomerular basement membrane; glomerular filtration; in vivo; inhibition of autophagy; injured; intercellular communication; mesangial cell; mouse model; novel; overexpression; paracrine; paxillin; podocyte; response; senescence; slit diaphragm; therapeutic target

DESCRIPTION (provided by applicant): Diabetic Nephropathy is a highly prevalent and debilitating disease, which is characterized morphologically by degenerative changes of renal podocytes associated with a variable extent of foot process effacement, thickening of glomerular basement membranes, endothelial cell injury, and expansion of the mesangial matrix, all contributing to progressive renal failure. It has become clear in past years that podocytes are injured very early in the course of the disease, and studies on Diabetic Nephropathy have focused primarily on podocyte depletion as mediators of glomerular injury and proteinuria, either by detachment or by apoptosis. However, recent work by our group and others identified features of accelerated senescence in glomeruli of patients with Diabetic Nephropathy. Cellular senescence is an alternative cellular response to prolonged metabolic stress as seen in diabetes, and is characterized by irreversible cell cycle arrest. However, senescent cells remain metabolically active, and recent studies identified the Senescence-Associated Secretory Phenotype (SASP) as a novel means of intercellular communication. Autophagy is closely associated with the senescent phenotype, and is thought to serve as a regulator of both apoptosis and senescence. This project aims to define the role of senescence and autophagy in mediating glomerular injury in Diabetic Nephropathy, and to elucidate the potential role of the SASP in disease progression. To this end, the candidate aims to: 1) Study the role of hic-5 in promoting a senescent phenotype in podocytes in response to sustained diabetic stress through activation of an anchorage-dependent cell survival mechanism in vitro and in vivo, by use of cultured podocytes, mouse models of disease and subsequent validation of results in a collection of human kidney biopsies; 2) Establish the contribution of autophagy to promoting podocyte senescence in diabetic nephropathy in vitro and in vivo by use of cultured podocytes, mouse models of disease and subsequent validation of results in a collection of human kidney biopsies; and 3) Investigate the role of the Senescence Associated Secretory Phenotype in disease progression in the glomerulus by using the podocyte "secretome" as a platform to identify molecular mediators of glomerular injury, followed by validation using co-culture models. Understanding the role of senescence and its associated factors in promoting glomerular injury and intraglomerular cross talk in diabetic nephropathy and potentially other glomerular diseases may help to identify novel and specific therapeutic targets.

描述(申请人提供)：糖尿病肾病是一种高度流行和衰弱的疾病，其形态特征是肾足细胞退行性改变，与不同程度的足突消失、肾小球基底膜增厚、内皮细胞损伤和系膜基质扩张有关，所有这些都有助于进行性肾功能衰竭。在过去的几年中，足细胞在疾病的早期就受到了损伤，对糖尿病肾病的研究主要集中在足细胞耗竭作为肾小球损伤和蛋白尿的介体，无论是通过脱离还是通过细胞凋亡。然而，我们小组和其他人最近的工作发现了糖尿病肾病患者肾小球加速衰老的特征。细胞衰老是一种对长期代谢应激的替代细胞反应，如糖尿病，其特征是不可逆转的细胞周期停滞。然而，衰老细胞仍然保持代谢活性，最近的研究发现衰老相关分泌表型(SASP)是一种新的细胞间通讯方式。自噬与衰老表型密切相关，被认为是细胞凋亡和衰老的调节因子。本项目旨在明确衰老和自噬在糖尿病肾病肾小球损伤中的作用，并阐明SASP在疾病进展中的潜在作用。为此，候选者的目标是：1)通过利用体外和体内培养的足细胞、小鼠疾病模型和随后收集的人类肾脏活检组织的结果验证，研究HIC-5在促进足细胞衰老表型中的作用，以应对持续的糖尿病应激；2)通过利用培养的足细胞、小鼠疾病模型和随后在收集的人类肾脏活检组织中验证的结果，研究HIC-5在促进糖尿病肾病足细胞衰老中的作用；3)以足细胞“分泌组”为平台，研究衰老相关分泌表型在肾小球疾病进展中的作用，并利用共培养模型进行验证。了解衰老及其相关因素在糖尿病肾病和潜在其他肾小球疾病中促进肾小球损伤和肾小球内串扰的作用可能有助于确定新的和特定的治疗靶点。