Bard Frédéric, Malhotra Vivek
Cell and Developmental Biology Department, University of California San Diego, La Jolla, California 92093, USA.
Annu Rev Cell Dev Biol. 2006;22:439-55. doi: 10.1146/annurev.cellbio.21.012704.133126.
In the trans-Golgi network (TGN), proteins are sorted for transport to the endosomes, plasma membrane, preceding Golgi cisternae, and endoplasmic reticulum. The formation of clathrin-coated vesicles for transport to the endosomes and of COP-I-coated vesicles for retrograde trafficking is fairly well characterized at the molecular level. We describe our current understanding of the TGN-to-cell-surface carriers, with a specific focus on the components involved in membrane fission. Inhibiting the fission machinery promotes growth of transport carriers into large tubules that remain attached to the TGN. Overactivating this machinery, on the other hand, vesiculates the TGN. To understand how membrane fission is regulated by cargo to form transport carriers yet prevents complete vesiculation of the TGN remains a daunting challenge. We discuss these issues with regard to TGN-to-cell-surface transport carriers.
在反式高尔基体网络(TGN)中,蛋白质被分类以便运输到内体、质膜、前高尔基体潴泡和内质网。在分子水平上,用于运输到内体的网格蛋白包被囊泡以及用于逆行运输的COP-I包被囊泡的形成已得到相当充分的表征。我们阐述了目前对TGN到细胞表面载体的理解,特别关注参与膜裂变的成分。抑制裂变机制会促进运输载体生长成仍附着于TGN的大管状结构。另一方面,过度激活该机制会使TGN形成囊泡。理解货物如何调节膜裂变以形成运输载体同时又防止TGN完全囊泡化仍然是一项艰巨的挑战。我们将围绕TGN到细胞表面的运输载体来讨论这些问题。