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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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 |
work_keys_str_mv |
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1725129194615078912 |