生物
海马结构
神经突
基因剔除小鼠
转基因小鼠
细胞生物学
生长锥
微管相关蛋白
转基因
τ蛋白
神经科学
微管
基因
轴突
内科学
遗传学
阿尔茨海默病
体外
医学
疾病
作者
Hana N. Dawson,Adriana Ferreira,Michele V. Eyster,Nupur Ghoshal,Lester I. Binder,Michael Peter Vitek
标识
DOI:10.1242/jcs.114.6.1179
摘要
Conflicting evidence supports a role for tau as an essential neuronal cytoskeletal protein or as a redundant protein whose function can be fulfilled by other microtubule-associated proteins. To investigate the function of tau in axonogenesis, we created tau deficient mice by disrupting the TAU gene. The engineered mice do not express the tau protein, appear physically normal and are able to reproduce. In contrast to a previously reported tau knockout mouse, embryonic hippocampal cultures from tau deficient mice show a significant delay in maturation as measured by axonal and neuritic extensions. The classic technique of selectively enhancing axonal growth by growth on laminin substrates failed to restore normal neuronal maturation of tau knockout neurons. By mating human TAU-gene transgenic and tau knockout mice, we reconstituted tau-deficient neurons with human tau proteins and restored a normal pattern of axonal growth and neuronal maturation. The ability of human tau proteins to rescue tau-deficient mouse neurons confirms that tau expression affects the rate of neurite extension.
科研通智能强力驱动
Strongly Powered by AbleSci AI