Link C D
Department of Biological Sciences, University of Denver, CO 80208, USA.
Proc Natl Acad Sci U S A. 1995 Sep 26;92(20):9368-72. doi: 10.1073/pnas.92.20.9368.
Transgenic Caenorhabditis elegans nematodes have been engineered to express potentially amyloidic human proteins. These animals contain constructs in which the muscle-specific unc-54 promoter/enhancer of C. elegans drives the expression of the appropriate coding regions derived from human cDNA clones. Animals containing constructs expressing the 42-amino acid beta-amyloid peptide (derived from human amyloid precursor protein cDNA) produce muscle-specific deposits immunoreactive with anti-beta-amyloid polyclonal and monoclonal antibodies. A subset of these deposits also bind the amyloid-specific dye thioflavin S, indicating that these deposits have the tinctural characteristics of classic amyloid. Co-expression of beta-peptide and transthyretin, a protein implicated in preventing the formation of insoluble beta-amyloid, leads to a dramatic reduction in the number of dye-reactive deposits. These results suggest that this invertebrate model may be useful for in vivo investigation of factors that modulate amyloid formation.
转基因秀丽隐杆线虫已被设计用于表达具有潜在淀粉样特性的人类蛋白质。这些动物含有构建体,其中秀丽隐杆线虫的肌肉特异性unc-54启动子/增强子驱动源自人类cDNA克隆的适当编码区的表达。含有表达42个氨基酸的β-淀粉样肽(源自人类淀粉样前体蛋白cDNA)的构建体的动物会产生与抗β-淀粉样多克隆和单克隆抗体发生免疫反应的肌肉特异性沉积物。这些沉积物的一个子集也与淀粉样特异性染料硫黄素S结合,表明这些沉积物具有经典淀粉样物质的染色特征。β-肽与转甲状腺素蛋白(一种与防止不溶性β-淀粉样物质形成有关的蛋白质)的共表达导致染料反应性沉积物的数量显著减少。这些结果表明,这种无脊椎动物模型可能有助于在体内研究调节淀粉样物质形成的因素。