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PMID: 15632110 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Live imaging of bidirectional traffic from the ERGIC.

Journal of cell science ·Vol. 118 ·No. Pt 2 ·2005-01-15 ·Pages 357-67

Ben-Tekaya H, Miura K, Pepperkok R, Hauri HP

Abstract

The endoplasmic reticulum-Golgi intermediate compartment (ERGIC) defined by the cycling lectin ERGIC-53 consists of tubulovesicular clusters, but it is unknown if these membranes are transport vehicles or stationary entities. Here, we show by live imaging that GFP-ERGIC-53 mainly localizes to long-lived stationary and some short-lived highly mobile elements. Unlike the anterograde marker VSV-G-GFP, GFP-ERGIC-53 does not vectorially move to the Golgi upon exit from the ERGIC, as assessed by a novel quantitative vector field method. Dual-color imaging of GFP-ERGIC-53 and a secretory protein (signal-sequence-tagged dsRed) reveals that the stationary elements are sites of repeated sorting of retrograde and anterograde cargo, and are interconnected by highly mobile elements. These results suggest that the ERGIC is stationary and not simply a collection of mobile carriers that mediate protein traffic from endoplasmic reticulum to Golgi.

MeSH Terms
Biological Transport, Active/physiology Endoplasmic Reticulum/metabolism Golgi Apparatus/metabolism Green Fluorescent Proteins/metabolism HeLa Cells Humans Mannose-Binding Lectins/metabolism Membrane Proteins/metabolism Protein Transport/physiology
Chemicals
LMAN1 protein, human Mannose-Binding Lectins Membrane Proteins Green Fluorescent Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ben-Tekaya Houchaima
Department of Pharmacology and Neurobiology, Biozentrum, University of Basel, Klingelbergstrasse 70, 4056 Basel, Switzerland.
Miura Kota
Pepperkok Rainer
Hauri Hans-Peter
Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
0021-9533
Published
2005-01-15
Epub
2005-00-04
Pages
357-67
Language
English
Region
England
NLM ID
0052457
Subset
IM
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