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Alcohol-Induced Liver Fibrosis: An In Vitro Model

Alcohol-Induced Liver Fibrosis: An In Vitro Model
酒精引起的肝纤维化:体外模型
批准号:
6941392
负责人:
MARCOS ROJKIND
金额:
$34.2万
依托单位国家:
美国
项目类别:
财政年份:
1992
资助国家:
美国
项目状态:
已结题
起止时间:
1992-04-01 至 2007-08-31

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中文摘要
翻译
描述(由申请人提供):酒精性肝硬化仍然是西半球发病率和死亡率的主要原因。它对肝星状细胞(肝脏中主要的I型胶原生成细胞)的纤维化作用部分是由其第一代谢物乙醛介导的。该化合物通过过氧化氢积累和转化生长因子- β (tgf - β)上调的机制诱导I型胶原基因转录激活。然而,这些作用背后的分子机制仍有待阐明。因此,在本应用中,我们提出旨在揭示由乙醛触发的关键事件的实验,这些事件将直接侵犯胶原蛋白基因上调。具体而言,我们提出以下目标:
英文摘要
DESCRIPTION (provided by applicant): Alcoholic cirrhosis continues to be a major cause of morbidity and mortality in the Western hemisphere. Its fibrogenic actions on hepatic stellate cells, the main type I collagen-producing cells in the liver, are mediated in part, by its first metabolite acetaldehyde. This compound induces the transcriptional activation of the type I collagen genes by a mechanism involving accumulation of hydrogen peroxide and up-regulation of transforming growth factor-beta (TGF-beta). However, molecular mechanisms underlying these effects remain to be elucidated. Thus, in this application we propose experiments aimed at unraveling key events triggered by acetaldehyde that will directly infringe upon collagen gene upregulation. Specifically, we propose the following aims: 1) To investigate key molecular mechanisms involved in the early response to acetaldehyde leading to COL1A2 upregulation. 2) To investigate molecular mechanisms involved in the late response to acetaldehyde leading to upregulation of TGF-beta gene expression and priming of HSC to respond more efficiently to this cytokine and 3) To study the role of acetaldehyde in the activation of latent TGF-beta in HSC. A better characterization of molecular events involved in acetaldehyde-dependent up-regulation of the type I collagen genes will allow us to establish key sites for therapeutic intervention. Moreover, from our experiments we expect to define pathways connecting acetaldehyde-mediated events with hydrogen peroxide and TGF-beta leading to the establishment of an autocrine loop that sustains fibrogenesis. Our long-term goal is to unravel molecular mechanisms involved in acetaldehyde-mediated fibrogenesis and develop novel therapies to inhibit collagen deposition and/or remove fibrous scar collagen from the liver.
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INTERLEUKIN 6 ROLE IN ALCOHOLIC LIVER CIRRHOSIS
INTERLEUKIN 6 ROLE IN ALCOHOLIC LIVER CIRRHOSIS
INTERLEUKIN 6 ROLE IN ALCOHOLIC LIVER CIRRHOSIS
  • 批准号:
    6629598
  • 项目类别:
  • 资助金额:
    $6.29万
  • 财政年份:
    1995
  • 负责人:
    MARCOS ROJKIND
  • 依托单位:
INTERLEUKIN 6 ROLE IN ALCOHOLIC LIVER CIRRHOSIS
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