Lippincott-Schwartz J, Cole N B, Donaldson J G
Cell Biology and Metabolism Branch, NICHD, NIH, Bethesda, MD 20892-5430, USA.
Histochem Cell Biol. 1998 May-Jun;109(5-6):449-62. doi: 10.1007/s004180050247.
The secretory apparatus within all eukaryotic cells comprises a dynamic membrane system with bidirectional membrane transport pathways and overlapping compartmental boundaries. Membrane traffic and organelle biogenesis/maintenance are fundamentally linked within this system, with perturbations in membrane traffic quickly leading to changes in organelle structure and identity. Dissection of the molecular basis of these properties in yeast and mammalian cells has revealed a crucial role for the cytoplasmic protein complex ARF1/COPI, which undergoes regulated assembly and disassembly with membranes. ARF1/COPI appears to be involved in the formation and maintenance of the Golgi complex, which is the receiving and delivery station for all secretory traffic. ARF1-GTP, through assembly of COPI to membranes and, possibly, through activation of PLD, is likely to promote the formation and maturation of pre-Golgi intermediates into Golgi elements, whereas ARF-GDP causes COPI dissociation and stimulates the formation of retrograde transport structures that recycle Golgi membrane back to the ER. These processes are appear to underlie the coupling of organelle biogenesis and membrane trafficking within cells, allowing the size and shape of secretory organelles to be altered in response to changing cellular needs. Future work needs to address how the activation and localization of ARF1/COPI to membranes as well as other related factors are temporally and spatially regulated, and by what mechanism they transform membrane shape and dynamics to facilitate protein transport and compartmental functioning.
所有真核细胞内的分泌装置都包含一个具有双向膜运输途径和重叠区室边界的动态膜系统。在这个系统中,膜运输与细胞器的生物发生/维持在根本上是相互关联的,膜运输的扰动会迅速导致细胞器结构和特性的改变。对酵母和哺乳动物细胞中这些特性的分子基础进行剖析后发现,细胞质蛋白复合物ARF1/COPI起着关键作用,它会与膜进行有调控的组装和解聚。ARF1/COPI似乎参与了高尔基体复合物的形成和维持,高尔基体是所有分泌运输的接收和输送站。ARF1-GTP通过将COPI组装到膜上,可能还通过激活磷脂酶D,可能促进高尔基体前体中间体形成并成熟为高尔基体元件,而ARF-GDP则导致COPI解离,并刺激逆行运输结构的形成,将高尔基体膜循环回内质网。这些过程似乎是细胞内细胞器生物发生与膜运输耦合的基础,使分泌细胞器的大小和形状能够根据细胞需求的变化而改变。未来的工作需要解决ARF1/COPI在膜上的激活和定位以及其他相关因子是如何在时间和空间上受到调控的,以及它们通过何种机制改变膜的形状和动力学以促进蛋白质运输和区室功能。