Shah Jagesh V, Cleveland Don W
Ludwig Institute for Cancer Research, and Departments of Cellular and Molecular Medicine and Neurosciences, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Curr Opin Cell Biol. 2002 Feb;14(1):58-62. doi: 10.1016/s0955-0674(01)00294-0.
The bulk of neuronally synthesized proteins destined for the axon is transported in a phase of transport approximately 100 times slower (1mm/day) than the vesicular traffic of fast axonal transport (100mm/day). Of late, a number of studies have shed considerable light on the controversies and mechanisms surrounding this slow phase of axonal transport. Along-standing controversy has centered on the form of the transported proteins. One major transport cargo, neurofilament protein, has now been seen in a number of contexts to be transported primarily in a polymeric form, whereas a second cargo tubulin is transported as a small oligomer. The development of techniques to visualize the slow transport process in live cells has demonstrated that instantaneous motions of transported neurofilaments, and presumably other slow transport cargoes, are fast, bidirectional and interspersed with long pauses. This and additional biochemical efforts indicate that traditional fast motors, such as conventional kinesin and dynein, are responsible for these fast motions.
大部分注定要运输到轴突的神经元合成蛋白,其运输阶段的速度比快速轴突运输的囊泡运输速度(每天100毫米)慢约100倍(每天1毫米)。最近,一些研究为围绕轴突运输这一缓慢阶段的争议和机制提供了相当多的线索。一个长期存在的争议集中在运输蛋白的形式上。一种主要的运输货物,神经丝蛋白,现在在许多情况下被发现主要以聚合物形式运输,而另一种货物微管蛋白则以小寡聚体形式运输。用于可视化活细胞中缓慢运输过程的技术发展表明,运输的神经丝以及可能其他缓慢运输货物的瞬时运动是快速的、双向的,并且穿插着长时间的停顿。这一点以及其他生化研究表明,传统的快速运动蛋白,如传统的驱动蛋白和动力蛋白,负责这些快速运动。