INTERACTIONS OF FIBRINOGEN WITH p75NTR
INTERACTIONS OF FIBRINOGEN WITH p75NTR
批准号:
6906782
负责人:
Katerina Akassoglou
金额:
$34.96万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-03-18 至 2010-01-31
关键词:
Schwann cellscell growth regulationcell population studycentral nervous systemfibrinfibrinogengenetically modified animalsgrowth factor receptorshistologyinflammationlaboratory mousemultiple sclerosismyelinopathynerve injurynervous system disorder chemotherapynervous system regenerationneuropathologyneurotrophic factorsperipheral nervous systemprotein degradationprotein protein interactionprotein structure functionreceptor bindingreceptor expressiontissue /cell culture
中文摘要
描述(由申请人提供):纤维蛋白酶是一种血液来源的蛋白质,在与血管破裂相关的疾病(如中风、多发性硬化症(MS)和脑胶质母细胞瘤)后沉积在神经系统中。我们以前的研究表明,在小鼠遗传或纤维蛋白原缺乏的纤维蛋白抑制周围神经再生和加剧炎症脱髓鞘在中枢神经系统的动物模型MS。我们的长期目标是确定的分子和细胞界面,纤维蛋白利用诱导神经系统病理。
该建议的具体假设是,纤维蛋白与p75神经营养因子受体(p75 NTR)相互作用,以介导其在神经系统中的作用。我们的假设是基于以下观察:1:纤维蛋白原及其衍生物直接结合p75 NTR,因此可能直接调节受体功能; 2。p75 NTR在体内的表达调节纤维蛋白及其衍生物在神经系统中的生物利用度。3.纤维蛋白原及其降解产物通过p75 NTR介导多种生存反应。
基于这些观察结果,本建议的实验重点是对p75 NTR与纤维蛋白原相互作用的生物化学、体内和体外分析。具体目标是:1.建立p75 NTR与纤维蛋白原及其衍生物的生物化学相互作用,2:确定PNS和CNS中表达p75 NTR的细胞类型中纤维蛋白(原)诱导的生物学效应,3:建立p75 NTR/纤维蛋白相互作用在神经再生和炎性脱髓鞘中的作用。由于p75 NTR在成人神经系统中响应于损伤而上调,因此鉴定p75 NTR与纤维蛋白的分子相互作用可能为以血管损伤、内皮细胞活化和组织修复能力降低为特征的多种疾病的药理学干预提供损伤特异性靶点。
英文摘要
DESCRIPTION (provided by applicant): Fibrin is a blood-derived protein deposited in the nervous system after disease associated with vasculature rupture; such as stroke, multiple sclerosis (MS) and brain glioblastomas. Our previous studies in mice genetically or pharmacologically deficient in fibrinogen demonstrated that fibrin inhibits peripheral nerve regeneration and exacerbates inflammatory demyelination in the central nervous system in an animal model for MS. Our long term goal is to identify the molecular and cellular interface that fibrin utilizes to induce nervous system pathology.
The specific hypothesis of this proposal is that fibrin interacts with the p75 neurotrophin receptor (p75NTR) to mediate its effects in the nervous system. Our hypothesis is based on the observations that 1: Fibrinogen and its derivatives directly bind to p75NTR and thus may directly modulate receptor function; 2. p75NTR expression in vivo regulates the bioavailability of fibrin and its derivatives in the nervous system. 3. Fibrinogen and its degradation products mediate diverse survival responses via p75NTR.
Based on these observations, the experimental focus of this proposal is on the biochemical, in vivo and in vitro analysis of the p75NTR interactions with fibrinogen. The specific aims are to: 1. Establish the biochemical interactions of p75NTR with fibrinogen and its derivatives, 2: Determine the biological effects induced by fibrin(ogen) in p75NTR - expressing cell types in the PNS and CNS and 3: Establish the contribution of p75NTR / fibrin interactions in nerve regeneration and inflammatory demyelination. Since p75NTR is upregulated in the adult nervous system in response to injury, identifying the molecular interactions of p75NTR with fibrin could potentially provide injury-specific targets for pharmacological intervention in a variety of diseases characterized by vascular damage, endothelial cell activation and decreased capacity for tissue repair.
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会议论文
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