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Fibrinolytic Pathways in Lung Injury and Repair

肺损伤和修复中的纤溶途径

基本信息

批准号：
7667898
负责人：
Steven Idell
金额：
$ 160.91万
依托单位：
UNIVERSITY OF TEXAS HLTH CTR AT TYLER
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-09-01 至 2012-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7667898
关键词：
Fibrinolytic Pathways Lung Injury Repair

项目摘要

DESCRIPTION (provided by applicant): Abnormalities in the plasminogen activator (PA) pathways have been implicated in the pathogenesis of acute lung (All) and pleural injury. Recent interventional trials suggest that targeting these pathways can reduce mortality in sepsis and protect against acute lung or pleural injury. The Project Leaders of this PPG have developed evidence that these pathways can influence ALI and pleural injury through newly recognized mechanisms. However the pathogenic mechanisms that link the PA pathways to ALI and pleural injury are poorly understood and are likely to involve non-proteolytic signal-transducing pathways. Our thematic objective is to address this gap by defining novel mechanisms by which urokinase (uPA), its receptor (uPAR), other novel uPA receptors and its inhibitor PAI-1 influence the course of inflammation, remodeling of transitional matrix and accelerated fibrosis in ALI and pleural injury. In Project 1, pathways that regulate PAI-1 and uPAR expression by the.mesothelium at the posttranscriptional level will be defined and a novel fibrinolytic intervention to prevent pleural loculation will be further evaluated. Project 2 will elucidate novel posttranscriptional mechanisms by which uPA and uPAR are regulated by the lung epithelium. Project 3 will define novel pathways by which uPA interacts with cell surface signaling adapter molecules to regulate pulmonary vasoconstriction and lung edema after ALI and ascertain the role of defensin in the process. These interactive projects derive from active programs directed by experienced Project Leaders and are now oriented to our thematic objective. In vitro, in vivo and interventional methods will be used. This PPG will accelerate the acquisition of new, clinically relevant information that will hasten the development of better treatments for ALI and/or pleural injury.

描述（由申请人提供）：纤溶酶原激活物（PA）通路的异常与急性肺（All）和胸膜损伤的发病机制有关。最近的介入试验表明，靶向这些途径可以降低败血症的死亡率，并防止急性肺或胸膜损伤。该PPG的项目负责人已经开发出证据，证明这些途径可以通过新认识的机制影响ALI和胸膜损伤。然而，将PA通路与ALI和胸膜损伤联系起来的致病机制尚不清楚，可能涉及非蛋白水解信号转导通路。我们的主题目标是通过定义尿激酶（uPA）、其受体（uPAR）、其他新型uPA受体及其抑制剂PAI-1影响ALI和胸膜损伤中炎症过程、移行基质重塑和加速纤维化的新机制来解决这一空白。在项目1中，调节PAI-1和uPAR表达的途径。将定义转录后水平的间皮细胞，并进一步评估一种新的纤维蛋白溶解干预措施，以防止胸膜定位。项目2将阐明uPA和uPAR受肺上皮调节的新的转录后机制。项目3将定义uPA与细胞表面信号适配器分子相互作用调节ALI后肺血管收缩和肺水肿的新途径，并确定防御素在这一过程中的作用。这些互动项目源于经验丰富的项目负责人指导的积极项目，现在面向我们的主题目标。将采用体外、体内和介入性方法。该PPG将加速获得新的临床相关信息，从而加快开发更好的治疗ALI和/或胸膜损伤的方法。

项目成果

期刊论文数量（22）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

tPA regulates pulmonary vascular activity through NMDA receptors.

tPA 通过 NMDA 受体调节肺血管活性。

DOI：
10.1152/ajplung.00429.2010
发表时间：
2011
期刊：
American journal of physiology. Lung cellular and molecular physiology
影响因子：
0
作者：
Nassar,Taher;Bdeir,Khalil;Yarovoi,Serge;Fanne,RamiAbu;Murciano,Juan-Carlos;Idell,Steven;Allen,TimothyCraig;Cines,DouglasB;Higazi,AbdAl-Roof
通讯作者：
Higazi,AbdAl-Roof

Activation and degradation of protein C by primary rabbit pleural mesothelial cells.

原代兔胸膜间皮细胞对蛋白 C 的激活和降解。

DOI：
10.1007/s00408-005-2566-z
发表时间：
2006
期刊：
Lung
影响因子：
5
作者：
Iakhiaev,Alexei;Idell,Steven
通讯作者：
Idell,Steven

Regulation of airway contractility by plasminogen activators through N-methyl-D-aspartate receptor-1.

DOI：
10.1165/rcmb.2009-0257oc
发表时间：
2010-12
期刊：
American journal of respiratory cell and molecular biology
影响因子：
6.4
作者：
T. Nassar;S. Yarovoi;R. A. Fanne;S. Akkawi;Mahmud Jammal;T. Allen;S. Idell;D. Cines;A. Higazi
通讯作者：
T. Nassar;S. Yarovoi;R. A. Fanne;S. Akkawi;Mahmud Jammal;T. Allen;S. Idell;D. Cines;A. Higazi

Blood-brain barrier permeability and tPA-mediated neurotoxicity.

DOI：
10.1016/j.neuropharm.2009.12.017
发表时间：
2010-06
期刊：
NEUROPHARMACOLOGY
影响因子：
4.7
作者：
Abu Fanne, Rami;Nassar, Taher;Yarovoi, Sergei;Rayan, Anwar;Lamensdorf, Itschak;Karakoveski, Michael;Vadim, Polianski;Jammal, Mahmud;Cines, Douglas B.;Higazi, Abd Al-Roof
通讯作者：
Higazi, Abd Al-Roof

Generation and release of nitrotyrosine O-sulfate by HepG2 human hepatoma cells upon SIN-1 stimulation: identification of SULT1A3 as the enzyme responsible.