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从反式高尔基体网络向周边内体移动的长距离运输载体的超微结构。

Ultrastructure of long-range transport carriers moving from the trans Golgi network to peripheral endosomes.

作者信息

Polishchuk Roman S, San Pietro Enrica, Di Pentima Alessio, Teté Stefano, Bonifacino Juan S

机构信息

Department of Cell Biology and Oncology, Consorzio Mario Negri Sud, 66030, Santa Maria Imbaro (Chieti), Italy.

出版信息

Traffic. 2006 Aug;7(8):1092-103. doi: 10.1111/j.1600-0854.2006.00453.x. Epub 2006 Jun 19.

DOI:10.1111/j.1600-0854.2006.00453.x
PMID:16787435
Abstract

The delivery of mannose 6-phosphate receptors carrying lysosomal hydrolases from the trans-Golgi network (TGN) to the endosomal system is mediated by selective incorporation of the receptor-hydrolase complexes into vesicular transport carriers (TCs) that are coated with clathrin and the adaptor proteins, GGA and AP-1. Previous electron microscopy (EM) and biochemical studies have shown that these TCs consist of spherical coated vesicles with a diameter of 60-100 nm. The use of fluorescent live cell imaging, however, has revealed that at least some of this transport relies on a subset of apparently larger and highly pleiomorphic carriers that detach from the TGN and translocate toward the peripheral cytoplasm until they meet with distally located endosomes. The ultrastructure of such long-range TCs has remained obscure because of the inability to examine by conventional EM the morphological details of rapidly moving organelles. The recent development of correlative light-EM has now allowed us to obtain ultrastructural 'snapshots' of these TCs immediately after their formation from the TGN in live cells. This approach has revealed that such carriers range from typical 60- to 100-nm clathrin-coated vesicles to larger, convoluted tubular-vesicular structures displaying several coated buds. We propose that this subset of TCs serve as vehicles for long-range distribution of biosynthetic or recycling cargo from the TGN to the peripheral endosomes.

摘要

携带溶酶体水解酶的甘露糖6-磷酸受体从反式高尔基体网络(TGN)向内体系统的转运,是通过受体-水解酶复合物选择性地掺入被网格蛋白以及衔接蛋白GGA和AP-1包被的囊泡运输载体(TCs)来介导的。先前的电子显微镜(EM)和生化研究表明,这些TCs由直径为60-100nm的球形包被囊泡组成。然而,荧光活细胞成像的应用揭示,至少部分这种转运依赖于一些明显更大且高度多形的载体,这些载体从TGN脱离并向周边细胞质转运,直到它们与位于远端的内体相遇。由于无法通过传统电子显微镜检查快速移动细胞器的形态细节,这种远程TCs的超微结构一直不清楚。相关光镜-电子显微镜技术的最新发展,现在使我们能够在活细胞中从TGN形成这些TCs后立即获得它们的超微结构“快照”。这种方法揭示,此类载体范围从典型的60-100nm网格蛋白包被囊泡到显示多个包被芽的更大、盘绕的管状-囊泡结构。我们提出,这种TCs子集作为从TGN向周边内体进行生物合成或再循环货物长距离运输的载体。

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