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In vivo contributions of collagen IV for structure, stability and function of basement membranes

In vivo contributions of collagen IV for structure, stability and function of basement membranes
IV 型胶原蛋白对基底膜结构、稳定性和功能的体内贡献
批准号:
5393763
负责人:
Professor Dr. Klaus von der Mark, Ph.D., since 9/2005
金额:
$0.0万
依托单位国家:
德国
项目类别:
Priority Programmes
财政年份:
2002
资助国家:
德国
项目状态:
已结题
起止时间:
2001-12-31 至 2007-12-31

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中文摘要
翻译
基底膜代表普遍存在的细胞外蛋白质基质,其由通过许多同源和异源二聚体蛋白质相互作用连接在一起的网络(层粘连蛋白、胶原IV)、寡聚体(串珠素)和特化蛋白质(巢蛋白、纤蛋白)形成。六种不同的胶原IV亚基链a1(IV)-a6(IV)以组织特异性方式聚集成三种不同的网络,形成定义不同基底层的完整性、稳定性和功能性的最重要的结构元件。主要亚型a1(IV)2a 2(IV)在整个发育阶段以及成年动物的大多数组织中表达,并被认为是任何发育阶段的基础。为了检验这一假设,我们在小鼠中产生了Col 4a 1/2基因座的敲除模型。有三个主要问题需要回答:(1)在缺乏主要形式的IV型胶原的情况下,基底膜样结构能否形成?(2)IV型胶原蛋白对胚胎发育至关重要吗?(3)IV型胶原缺乏对细胞生长、分化和细胞死亡有何影响?对IV型胶原缺陷胚胎的初步分析显示,在早期胚胎发生中基底膜具有意想不到的可塑性,但仍导致胚胎死亡。在与其他小鼠模型的背景下对这种新型模型系统的分析将进一步帮助定义单个基底膜组分的功能。
英文摘要
Basement membranes represent ubiquitous extracellular protein matrices, formed by networks (laminins, collagens IV), oligomers (perlecan) and specialized proteins (nidogens, fibulins) linked together by numerous homo- and heterodimeric protein interactions. Six distinct collagen IV subunit chains, a1(IV)-a6(IV), aggregate into three distinct networks in a tissue-specific manner forming the most important structural elements defining integrity, stability and functionality of different basal laminae. The major isoform a1(IV)2a2(IV) is expressed throughout all stages of development as well as in most tissues of adult animals and was assumed to be fundamental at any stage of development. In order to test this hypothesis, we generated a knock-out model of the Col4a1/2 locus in mice. Three major questions should be answered : (1) Can basement membrane-like structures form in the absence of the major form of collagen IV ? (2) Is collagen IV essential for embryonic development ? and (3) What are the consequences of collagen IV-deficiency on cell growth, differentiation and cell death ? The initial analysis of collagen IV-deficient embryos revealed an unexpected plasticity of basement membranes in early embryogenesis, but nevertheless resulted in embryonic lethality. The analysis of this novel model system in the context with other mouse models will further help to define the functions of individual basement membrane components.
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