Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.

The heat shock protein 90 (Hsp90) inhibitor geldanamycin (GA) has been shown to alter endosomal sorting, diverting cargo destined for the recycling pathway into the lysosomal pathway. Here we investigated whether GA also affects the sorting of cargo into the retrograde pathway from endosomes to the...

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Main Authors: Anne Berit Dyve Lingelem, Ieva Ailte Hjelseth, Roger Simm, Maria Lyngaas Torgersen, Kirsten Sandvig
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4445914?pdf=render
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spelling doaj-80cd133425514fad8f5723b268de9d9d2020-11-25T01:21:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01105e012921410.1371/journal.pone.0129214Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.Anne Berit Dyve LingelemIeva Ailte HjelsethRoger SimmMaria Lyngaas TorgersenKirsten SandvigThe heat shock protein 90 (Hsp90) inhibitor geldanamycin (GA) has been shown to alter endosomal sorting, diverting cargo destined for the recycling pathway into the lysosomal pathway. Here we investigated whether GA also affects the sorting of cargo into the retrograde pathway from endosomes to the Golgi apparatus. As a model cargo we used the bacterial toxin Shiga toxin, which exploits the retrograde pathway as an entry route to the cytosol. Indeed, GA treatment of HEp-2 cells strongly increased the Shiga toxin transport to the Golgi apparatus. The enhanced Golgi transport was not due to increased endocytic uptake of the toxin or perturbed recycling, suggesting that GA selectively enhances endosomal sorting into the retrograde pathway. Moreover, GA activated p38 and both inhibitors of p38 or its substrate MK2 partially counteracted the GA-induced increase in Shiga toxin transport. Thus, our data suggest that GA-induced p38 and MK2 activation participate in the increased Shiga toxin transport to the Golgi apparatus.http://europepmc.org/articles/PMC4445914?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Anne Berit Dyve Lingelem
Ieva Ailte Hjelseth
Roger Simm
Maria Lyngaas Torgersen
Kirsten Sandvig
spellingShingle Anne Berit Dyve Lingelem
Ieva Ailte Hjelseth
Roger Simm
Maria Lyngaas Torgersen
Kirsten Sandvig
Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.
PLoS ONE
author_facet Anne Berit Dyve Lingelem
Ieva Ailte Hjelseth
Roger Simm
Maria Lyngaas Torgersen
Kirsten Sandvig
author_sort Anne Berit Dyve Lingelem
title Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.
title_short Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.
title_full Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.
title_fullStr Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.
title_full_unstemmed Geldanamycin Enhances Retrograde Transport of Shiga Toxin in HEp-2 Cells.
title_sort geldanamycin enhances retrograde transport of shiga toxin in hep-2 cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description The heat shock protein 90 (Hsp90) inhibitor geldanamycin (GA) has been shown to alter endosomal sorting, diverting cargo destined for the recycling pathway into the lysosomal pathway. Here we investigated whether GA also affects the sorting of cargo into the retrograde pathway from endosomes to the Golgi apparatus. As a model cargo we used the bacterial toxin Shiga toxin, which exploits the retrograde pathway as an entry route to the cytosol. Indeed, GA treatment of HEp-2 cells strongly increased the Shiga toxin transport to the Golgi apparatus. The enhanced Golgi transport was not due to increased endocytic uptake of the toxin or perturbed recycling, suggesting that GA selectively enhances endosomal sorting into the retrograde pathway. Moreover, GA activated p38 and both inhibitors of p38 or its substrate MK2 partially counteracted the GA-induced increase in Shiga toxin transport. Thus, our data suggest that GA-induced p38 and MK2 activation participate in the increased Shiga toxin transport to the Golgi apparatus.
url http://europepmc.org/articles/PMC4445914?pdf=render
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