Segregation of sphingolipids and sterols during formation of secretory vesicles at the trans-Golgi network

被引:304
|
作者
Klemm, Robin W. [1 ]
Ejsing, Christer S. [1 ]
Surma, Michal A. [1 ]
Kaiser, Hermann-Josef [1 ]
Gerl, Mathias J. [1 ]
Sampaio, Julio L. [1 ]
de Robillard, Quentin [1 ]
Ferguson, Charles [1 ]
Proszynski, Tomasz J. [2 ]
Shevchenko, Andrej [1 ]
Simons, Kai [1 ]
机构
[1] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[2] Harvard Univ, Ctr Brain Sci, Cambridge, MA 02138 USA
来源
JOURNAL OF CELL BIOLOGY | 2009年 / 185卷 / 04期
关键词
PLASMA-MEMBRANE ATPASE; CELL-SURFACE DELIVERY; SACCHAROMYCES-CEREVISIAE; MASS-SPECTROMETRY; LIPID RAFTS; EPITHELIAL-CELLS; APICAL MEMBRANE; YEAST; PATHWAY; ERGOSTEROL;
D O I
10.1083/jcb.200901145
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The trans-Golgi network (TGN) is the major sorting station in the secretory pathway of all eukaryotic cells. How the TGN sorts proteins and lipids to generate the enrichment of sphingolipids and sterols at the plasma membrane is poorly understood. To address this fundamental question in membrane trafficking, we devised an immunoisolation procedure for specific recovery of post-Golgi secretory vesicles transporting a transmembrane raft protein from the TGN to the cell surface in the yeast Saccharomyces cerevisiae. Using a novel quantitative shotgun lipidomics approach, we could demonstrate that TGN sorting selectively enriched ergosterol and sphingolipid species in the immunoisolated secretory vesicles. This finding, for the first time, indicates that the TGN exhibits the capacity to sort membrane lipids. Furthermore, the observation that the immunoisolated vesicles exhibited a higher membrane order than the late Golgi membrane, as measured by C-Laurdan spectrophotometry, strongly suggests that lipid rafts play a role in the TGN-sorting machinery.
引用
收藏
页码:601 / 612
页数:12
相关论文
共 50 条
  • [1] In vitro formation of secretory vesicles from the trans-Golgi in yeast
    Ahmed, SU
    Schekman, R
    MOLECULAR BIOLOGY OF THE CELL, 2001, 12 : 337A - 337A
  • [2] Cholesterol is required for the formation of regulated and constitutive secretory vesicles from the trans-Golgi network
    Wang, YZ
    Thiele, C
    Huttner, WS
    TRAFFIC, 2000, 1 (12) : 952 - 962
  • [3] CELL-FREE FORMATION OF IMMATURE SECRETORY GRANULES AND CONSTITUTIVE SECRETORY VESICLES FROM TRANS-GOLGI NETWORK
    TOOZE, SA
    HUTTNER, WB
    METHODS IN ENZYMOLOGY, 1992, 219 : 81 - 93
  • [4] BREFELDIN-A INHIBITS THE FORMATION OF CONSTITUTIVE SECRETORY VESICLES AND IMMATURE SECRETORY GRANULES FROM THE TRANS-GOLGI NETWORK
    ROSA, P
    BARR, FA
    STINCHCOMBE, JC
    BINACCHI, C
    HUTTNER, WB
    EUROPEAN JOURNAL OF CELL BIOLOGY, 1992, 59 (02) : 265 - 274
  • [5] TRIMERIC G-PROTEINS OF THE TRANS-GOLGI NETWORK ARE INVOLVED IN THE FORMATION OF CONSTITUTIVE SECRETORY VESICLES AND IMMATURE SECRETORY GRANULES
    BARR, FA
    LEYTE, A
    MOLLNER, S
    PFEUFFER, T
    TOOZE, SA
    HUTTNER, WB
    FEBS LETTERS, 1991, 294 (03) : 239 - 243
  • [6] MAMMALIAN AND YEAST CYTOSOLIC FACTORS SUPPORT FORMATION OF NASCENT SECRETORY VESICLES FROM THE TRANS-GOLGI NETWORK
    WONG, WL
    SHIELDS, D
    MOLECULAR BIOLOGY OF THE CELL, 1995, 6 : 2306 - 2306
  • [7] Secretory cargo sorting at the trans-Golgi network
    Kienzle, Christine
    von Blume, Julia
    TRENDS IN CELL BIOLOGY, 2014, 24 (10) : 584 - 593
  • [8] Role of dynamin in the formation of transport vesicles from the trans-Golgi network
    Jones, SM
    Howell, KE
    Henley, JR
    Cao, H
    McNiven, MA
    SCIENCE, 1998, 279 (5350) : 573 - 577
  • [9] PROHORMONE PROCESSING IN THE TRANS-GOLGI NETWORK - ENDOPROTEOLYTIC CLEAVAGE OF PROSOMATOSTATIN AND FORMATION OF NASCENT SECRETORY VESICLES IN PERMEABILIZED CELLS
    XU, HX
    SHIELDS, D
    JOURNAL OF CELL BIOLOGY, 1993, 122 (06): : 1169 - 1184
  • [10] Phospholipase D stimulates release of nascent secretory vesicles from the trans-Golgi network
    Chen, YG
    Siddhanta, A
    Austin, CD
    Hammond, SM
    Sung, TC
    Frohman, MA
    Morris, AJ
    Shields, D
    JOURNAL OF CELL BIOLOGY, 1997, 138 (03): : 495 - 504