Moechars D, Dewachter I, Lorent K, Reversé D, Baekelandt V, Naidu A, Tesseur I, Spittaels K, Haute C V, Checler F, Godaux E, Cordell B, Van Leuven F
Experimental Genetics Group, Center for Human Genetics, Flemish Institute for Biotechnology, Katholieke Universiteit Leuven, B-3000 Leuven, Belgium.
J Biol Chem. 1999 Mar 5;274(10):6483-92. doi: 10.1074/jbc.274.10.6483.
Transgenic mice overexpressing different forms of amyloid precursor protein (APP), i.e. wild type or clinical mutants, displayed an essentially comparable early phenotype in terms of behavior, differential glutamatergic responses, deficits in maintenance of long term potentiation, and premature death. The cognitive impairment, demonstrated in F1 hybrids of the different APP transgenic lines, was significantly different from nontransgenic littermates as early as 3 months of age. Biochemical analysis of secreted and membrane-bound APP, C-terminal "stubs," and Abeta(40) and Abeta(42) peptides in brain indicated that no single intermediate can be responsible for the complex of phenotypic dysfunctions. As expected, the Abeta(42) levels were most prominent in APP/London transgenic mice and correlated directly with the formation of amyloid plaques in older mice of this line. Plaques were associated with immunoreactivity for hyperphosphorylated tau, eventually signaling some form of tau pathology. In conclusion, the different APP transgenic mouse lines studied display cognitive deficits and phenotypic traits early in life that dissociated in time from the formation of amyloid plaques and will be good models for both early and late neuropathological and clinical aspects of Alzheimer's disease.
过表达不同形式淀粉样前体蛋白(APP)(即野生型或临床突变体)的转基因小鼠,在行为、不同的谷氨酸能反应、长期增强维持缺陷和过早死亡方面表现出基本相当的早期表型。不同APP转基因品系的F1代杂种小鼠早在3个月大时就表现出与非转基因同窝小鼠显著不同的认知障碍。对脑部分泌型和膜结合型APP、C末端“残端”以及Abeta(40)和Abeta(42)肽的生化分析表明,没有单一的中间产物能导致这种复杂的表型功能障碍。正如预期的那样,Abeta(42)水平在APP/伦敦转基因小鼠中最为显著,并且与该品系老年小鼠中淀粉样斑块的形成直接相关。斑块与过度磷酸化tau的免疫反应性相关,最终预示着某种形式的tau病理学。总之,所研究的不同APP转基因小鼠品系在生命早期就表现出认知缺陷和表型特征,这些特征在时间上与淀粉样斑块的形成无关,将成为阿尔茨海默病早期和晚期神经病理学及临床方面的良好模型。