Cargando…
Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport
We recently reported that ERM (ezrin, radixin, moesin) proteins are involved in intracellular sorting of Shiga toxin (Stx) and its receptor globotriaosylceramide (Gb3), and that depletion of ezrin and moesin reduced retrograde Golgi transport of Stx. In the same study, we found that knockdown of Vps...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995726/ https://www.ncbi.nlm.nih.gov/pubmed/24778763 http://dx.doi.org/10.4161/cib.28129 |
_version_ | 1782312924369387520 |
---|---|
author | Kvalvaag, Audun Sverre Pust, Sascha Sandvig, Kirsten |
author_facet | Kvalvaag, Audun Sverre Pust, Sascha Sandvig, Kirsten |
author_sort | Kvalvaag, Audun Sverre |
collection | PubMed |
description | We recently reported that ERM (ezrin, radixin, moesin) proteins are involved in intracellular sorting of Shiga toxin (Stx) and its receptor globotriaosylceramide (Gb3), and that depletion of ezrin and moesin reduced retrograde Golgi transport of Stx. In the same study, we found that knockdown of Vps11, a core subunit of both the homotypic fusion and protein sorting (HOPS) complex and the class C core vacuole/endosome tethering factor (CORVET), increased retrograde transport of Stx and could counteract the inhibiting effect of moesin and ezrin knockdown. In this study we demonstrate that Vps11 knockdown also leads to increased Stx toxicity as well as increased retrograde transport and toxicity of ricin. Additionally, we show that knockdown of Vps11 restores the reduced Gb3 level observed after moesin depletion. |
format | Online Article Text |
id | pubmed-3995726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-39957262014-04-28 Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport Kvalvaag, Audun Sverre Pust, Sascha Sandvig, Kirsten Commun Integr Biol Short Communication We recently reported that ERM (ezrin, radixin, moesin) proteins are involved in intracellular sorting of Shiga toxin (Stx) and its receptor globotriaosylceramide (Gb3), and that depletion of ezrin and moesin reduced retrograde Golgi transport of Stx. In the same study, we found that knockdown of Vps11, a core subunit of both the homotypic fusion and protein sorting (HOPS) complex and the class C core vacuole/endosome tethering factor (CORVET), increased retrograde transport of Stx and could counteract the inhibiting effect of moesin and ezrin knockdown. In this study we demonstrate that Vps11 knockdown also leads to increased Stx toxicity as well as increased retrograde transport and toxicity of ricin. Additionally, we show that knockdown of Vps11 restores the reduced Gb3 level observed after moesin depletion. Landes Bioscience 2014-04-03 /pmc/articles/PMC3995726/ /pubmed/24778763 http://dx.doi.org/10.4161/cib.28129 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Short Communication Kvalvaag, Audun Sverre Pust, Sascha Sandvig, Kirsten Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport |
title | Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport |
title_full | Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport |
title_fullStr | Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport |
title_full_unstemmed | Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport |
title_short | Vps11, a subunit of the tethering complexes HOPS and CORVET, is involved in regulation of glycolipid degradation and retrograde toxin transport |
title_sort | vps11, a subunit of the tethering complexes hops and corvet, is involved in regulation of glycolipid degradation and retrograde toxin transport |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995726/ https://www.ncbi.nlm.nih.gov/pubmed/24778763 http://dx.doi.org/10.4161/cib.28129 |
work_keys_str_mv | AT kvalvaagaudunsverre vps11asubunitofthetetheringcomplexeshopsandcorvetisinvolvedinregulationofglycolipiddegradationandretrogradetoxintransport AT pustsascha vps11asubunitofthetetheringcomplexeshopsandcorvetisinvolvedinregulationofglycolipiddegradationandretrogradetoxintransport AT sandvigkirsten vps11asubunitofthetetheringcomplexeshopsandcorvetisinvolvedinregulationofglycolipiddegradationandretrogradetoxintransport |