Kanai Y, Hirokawa N
Department of Anatomy and Cell Biology, School of Medicine, University of Tokyo, Japan.
Neuron. 1995 Feb;14(2):421-32. doi: 10.1016/0896-6273(95)90298-8.
Tau is abundant in the axon, whereas MAP2 is found in the cell body and dendrites. To understand their differential localization, we performed transfection studies on primary cultured neurons using tagged tau, MAP2, MAP2C, and their chimeric/deletion mutants. We found that MAP2 was prevented from entering the axon by its N-terminal projection domain and that microtubule binding of tau was stronger in the axon than in the cell body and dendrites, whereas that of MAP2/MAP2C was tighter in the cell body and dendrites than in the axon. These binding properties were determined by their microtubule-binding domains and were suggested to be regulated by phosphorylation, at least in the case of tau. Thus, the suppressed axonal transit of MAP2 and locally regulated microtubule binding may play important roles for their sorting in neurons.
Tau蛋白在轴突中含量丰富,而MAP2则存在于细胞体和树突中。为了解它们的差异定位,我们使用标记的tau蛋白、MAP2、MAP2C及其嵌合/缺失突变体对原代培养的神经元进行了转染研究。我们发现,MAP2的N端突出结构域阻止其进入轴突,并且tau蛋白与微管的结合在轴突中比在细胞体和树突中更强,而MAP2/MAP2C与微管的结合在细胞体和树突中比在轴突中更紧密。这些结合特性由它们的微管结合结构域决定,并且至少在tau蛋白的情况下,提示受磷酸化调节。因此,MAP2轴突转运的抑制和局部调节的微管结合可能在它们在神经元中的分选过程中发挥重要作用。