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Coagulation Protease Signaling in Glomerular Disease

肾小球疾病中的凝血蛋白酶信号传导

基本信息

批准号：
9769012
负责人：
Bryce Andrew Kerlin
金额：
$ 15.33万
依托单位：
RESEARCH INST NATIONWIDE CHILDREN'S HOSP
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-09-25 至 2021-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9769012
关键词：
Antithrombin III Antithrombins Attenuated Biological Biology Blood coagulation Candidate Disease Gene Cause of Death Cell Culture Techniques Cell Differentiation process Cessation of life Coagulation Process Data Development Disease Progression Disease model End stage renal failure Exposure to Expression Profiling Family Fc Receptor Funding G-Protein-Coupled Receptors Gene Expression Genes Genetic Transcription Goals Health Care Costs Hematological Disease Hemostatic function High Prevalence Human Induction of Apoptosis Injury Investigation K-Series Research Career Programs Kidney Kidney Diseases Laboratories Lead Learning Life Ligation Measures Mediating Medical Research Mentors Microarray Analysis Mission Modeling Molecular Molecular Biology Molecular Target National Institute of Diabetes and Digestive and Kidney Diseases Nephrosis Nephrotic Syndrome Pathway interactions Peptide Hydrolases Pharmacology Physicians Plasma Positioning Attribute Pre-Clinical Model Process Protease Inhibitor Proteinase-Activated Receptors Proteins Proteinuria Prothrombin Public Health Publishing Puromycin Aminonucleoside Rattus Reagent Receptor Signaling Renal glomerular disease Research Research Personnel Research Training Resources Reverse Transcriptase Polymerase Chain Reaction Risk Role Scientist Severities Signal Pathway Signal Transduction Supplementation System Systems Biology Techniques Testing Thrombin Thrombin Receptor Time Training Programs United States Urologic Diseases base biological adaptation to stress career data integration differential expression effective therapy expectation experimental study inhibitor/antagonist injured kidney biopsy knock-down novel novel strategies novel therapeutic intervention podocyte pre-clinical programs public health relevance response side effect small hairpin RNA tool urinary virtual

项目摘要

DESCRIPTION (provided by applicant): There is a critical need to define the molecular signaling pathways that are the crucial regulators of thrombin- mediated podocyte injury without which, the development of targeted, safe and effective therapies for nephrotic syndrome is likely to remain limited. The overall objective of this proposal is to develop the career of a hemostasis physician-scientist who will learn to apply coagulation biology, molecular biology, molecular pharmacology, and systems biology techniques to define the molecular mechanisms of thrombin-mediated glomerular injury. The central hypothesis is that, during proteinuria, podocytes are exposed to thrombin which exacerbates podocyte injury via activation of protease activated receptors (PAR). Using established podocyte cell culture lines, the PAR species that are essential for thrombin-mediated apoptosis induction will be determined through anti-PAR antibody blockade, shRNA knock-down, and proximity ligation experiments. Supplementation with antithrombin, a non-specific thrombin inhibitor, is known to attenuate proteinuria in experimental nephrosis models. Thus, the mechanism of action by which antithrombin modifies proteinuria will be determined by pharmacologically manipulating the thrombin signaling axis at each molecular level and examining the impact of each condition on glomerular injury as measured by proteinuria. Using rat and human cultured podocytes, gene expression profiles and transcriptional networks will be evaluated to determine podocyte-specific transcriptional responses to thrombin exposure. Subsequently, these profiles and networks will be correlated with those of isolated rat glomeruli and existing gene expression profiles of glomeruli isolated from human NS renal biopsies to determine thrombin-dependent podocyte transcriptional responses that are relevant to human nephrotic syndrome and simultaneously inform the selection of appropriate preclinical models of these processes. A prioritized strategy will be employed to guide further investigation of high-value candidate genes and their biological pathways. This career development award is directly responsive to the mission of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) which is to "support medical research and research training" on "kidney, urologic, and hematologic diseases." Completion of the training program and research in this career development award is expected generate compelling preliminary data for the awardee to successfully compete for R01 funding to systematically analyze coagulation signaling in glomerular diseases.

描述（由申请人提供）：迫切需要定义作为凝血酶介导的足细胞损伤的关键调节因子的分子信号传导途径，否则，肾病综合征的靶向、安全和有效疗法的开发可能仍然有限。本提案的总体目标是发展止血医师科学家的职业生涯，他们将学习应用凝血生物学，分子生物学，分子药理学和系统生物学技术来确定凝血酶介导的肾小球损伤的分子机制。中心假设是，在蛋白尿期间，足细胞暴露于凝血酶，凝血酶通过蛋白酶激活受体（PAR）的激活加剧足细胞损伤。使用已建立的足细胞培养系，通过抗PAR抗体阻断、shRNA敲低和邻近连接实验确定凝血酶介导的细胞凋亡诱导所必需的PAR种类。已知补充抗凝血酶（一种非特异性凝血酶抑制剂）可减轻实验性肾病模型中的蛋白尿。因此，抗凝血酶改变蛋白尿的作用机制将通过在每个分子水平上连续操纵凝血酶信号传导轴并检查每种条件对肾小球损伤的影响（如通过蛋白尿测量的）来确定。使用大鼠和人培养的足细胞，将评价基因表达谱和转录网络，以确定足细胞对凝血酶暴露的特异性转录反应。随后，这些配置文件和网络将与分离的大鼠肾小球和现有的基因表达谱的肾小球分离的人NS肾活检，以确定凝血酶依赖性足细胞转录反应，是相关的人类肾病综合征，同时通知这些过程的适当的临床前模型的选择。优先策略将用于指导高价值候选基因及其生物学途径的进一步研究。该职业发展奖直接响应国家糖尿病、消化和肾脏疾病研究所（NIDDK）的使命，即“支持肾脏、泌尿系统和血液系统疾病的医学研究和研究培训”。“完成这项职业发展奖的培训计划和研究，预计将为获奖者成功竞争R01资金，系统地分析肾小球疾病中的凝血信号传导产生令人信服的初步数据。

项目成果

期刊论文数量（10）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Thrombosis of the Abdominal Veins in Childhood.

DOI：
10.3389/fped.2017.00188
发表时间：
2017
期刊：
Frontiers in pediatrics
影响因子：
2.6
作者：
Kumar R;Kerlin BA
通讯作者：
Kerlin BA

Venous thromboembolism in chronic pediatric heart disease is associated with substantial health care burden and expenditures.

慢性儿科心脏病中的静脉血栓栓塞与大量的医疗保健负担和支出相关。

DOI：
10.1002/rth2.12205
发表时间：
2019
期刊：
Research and practice in thrombosis and haemostasis
影响因子：
4.6
作者：
Woods,GaryM;Boulet,ShereeL;Texter,Karen;Yates,AndrewR;Kerlin,BryceA
通讯作者：
Kerlin,BryceA

An Orthogonal Array Optimization of Lipid-like Nanoparticles for mRNA Delivery in Vivo.

DOI：
10.1021/acs.nanolett.5b03528
发表时间：
2015-12-09
期刊：
Nano letters
影响因子：
10.8
作者：
Li B;Luo X;Deng B;Wang J;McComb DW;Shi Y;Gaensler KM;Tan X;Dunn AL;Kerlin BA;Dong Y
通讯作者：
Dong Y

Plasma Cytokine Profiling to Predict Steroid Resistance in Pediatric Nephrotic Syndrome.

DOI：
10.1016/j.ekir.2020.12.027
发表时间：
2021-03
期刊：
Kidney international reports
影响因子：
6
作者：
Agrawal S;Brier ME;Kerlin BA;Smoyer WE;Pediatric Nephrology Research Consortium
通讯作者：
Pediatric Nephrology Research Consortium