Litman P, Barg J, Rindzoonski L, Ginzburg I
Department of Neurobiology, Weizmann Institute of Science, Rehovot, Israel.
Neuron. 1993 Apr;10(4):627-38. doi: 10.1016/0896-6273(93)90165-n.
A primary neuronal cell culture derived from whole brains of fetal rats was used to analyze the subcellular localization of tau mRNA, employing nonisotopic detection by in situ hybridization. The culture exhibited a developmental differentiation pattern previously described for neuronal cells in vivo; i.e., a transition from immature to mature tau isoforms as well as segregation of tau into the axons. Our results demonstrate that unlike tubulin mRNA, which is confined to cell bodies, or MAP2 mRNA, which extends into dendrites, tau mRNA was observed to enter the proximal portion of the axon. This sorting of tau mRNA might explain how the tau protein could be selectively delivered to the axon and could have important implications for the development of neuronal polarity.
利用源自胎鼠全脑的原代神经元细胞培养物,通过原位杂交的非同位素检测来分析tau mRNA的亚细胞定位。该培养物呈现出先前在体内神经元细胞中描述的发育分化模式;即从不成熟tau异构体向成熟tau异构体的转变以及tau在轴突中的分离。我们的结果表明,与局限于细胞体的微管蛋白mRNA或延伸至树突的MAP2 mRNA不同,观察到tau mRNA进入轴突的近端部分。tau mRNA的这种分选可能解释了tau蛋白如何能够被选择性地递送至轴突,并且可能对神经元极性的发育具有重要意义。