Stephens D J, Pepperkok R
Cell Biophysics and Cell Biology Program, EMBL Heidelberg, Meyerhofstrasse 1, Germany.
J Cell Sci. 2001 Mar;114(Pt 6):1053-9. doi: 10.1242/jcs.114.6.1053.
Recent studies using GFP-tagged markers and time-lapse microscopy have allowed direct visualisation of membrane traffic in the secretory pathway in living mammalian cells. This work shows that larger membrane structures, 300-500 nm in size, are the vehicles responsible for long distance, microtubule-dependent ER-to-Golgi and trans-Golgi to plasma membrane transport of secretory markers. At least two retrograde transport pathways from the Golgi to the ER exist, both of which are proposed to involve a further class of long, tubular membrane carrier that forms from the Golgi and fuses with the ER. Together, this has challenged established transport models, raising the question of whether larger pleiomorphic structures, rather than small 60-80 nm transport vesicles, mediate long-range transport between the ER and Golgi and between the Golgi and plasma membrane.
最近使用绿色荧光蛋白标记物和延时显微镜的研究,使得在活的哺乳动物细胞中直接观察分泌途径中的膜运输成为可能。这项工作表明,尺寸为300 - 500纳米的较大膜结构,是负责分泌标记物从内质网到高尔基体以及从反式高尔基体到质膜的长距离、依赖微管运输的载体。至少存在两条从高尔基体到内质网的逆行运输途径,这两条途径都被认为涉及另一类由高尔基体形成并与内质网融合的长管状膜载体。总之,这对已有的运输模型提出了挑战,引发了一个问题,即是否是较大的多形结构而非60 - 80纳米的小运输囊泡介导了内质网与高尔基体之间以及高尔基体与质膜之间的长距离运输。