Unknown

Dataset Information

0

Uptake of Shiga-toxigenic Escherichia coli?SubAB by HeLa cells requires an actin- and lipid raft-dependent pathway.


ABSTRACT: The novel cytotoxic factor subtilase cytotoxin (SubAB) is produced mainly by non-O157 Shiga-toxigenic Escherichia coli (STEC). SubAB cleaves the molecular chaperone BiP/GRP78 in the endoplasmic reticulum (ER), leading to activation of RNA-dependent protein kinase (PKR)-like ER kinase (PERK), followed by caspase-dependent cell death. However, the SubAB uptake mechanism in HeLa cells is unknown. In this study, a variety of inhibitors and siRNAs were employed to characterize the SubAB uptake process. SubAB-induced BiP cleavage was inhibited by high concentrations of Dynasore, and methyl-?-cyclodextrin (m?CD) and Filipin III, but not suppressed in clathrin-, dynamin I/II-, caveolin1- and caveolin2-knockdown cells. We observed that SubAB treatment led to dramatic actin rearrangements, e.g. formation of plasma membrane blebs, with a significant increase in fluid uptake. Confocal microscopy analysis showed that SubAB uptake required actin cytoskeleton remodelling and lipid raft cholesterol. Furthermore, internalized SubAB in cells was found in the detergent-resistant domain (DRM) structure. Interestingly, IPA-3, an inhibitor of serine/threonine kinase p21-activated kinase (PAK1), an important protein of macropinocytosis, directly inhibited SubAB-mediated BiP cleavage and SubAB internalization. Thus, our findings suggest that SubAB uses lipid raft- and actin-dependent, but not clathrin-, caveolin- and dynamin-dependent pathways as its major endocytic translocation route.

SUBMITTER: Nagasawa S 

PROVIDER: S-EPMC4241268 | biostudies-literature | 2014 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Uptake of Shiga-toxigenic Escherichia coli SubAB by HeLa cells requires an actin- and lipid raft-dependent pathway.

Nagasawa Sayaka S   Ogura Kohei K   Tsutsuki Hiroyasu H   Saitoh Hisako H   Moss Joel J   Iwase Hirotaro H   Noda Masatoshi M   Yahiro Kinnosuke K  

Cellular microbiology 20140617 10


The novel cytotoxic factor subtilase cytotoxin (SubAB) is produced mainly by non-O157 Shiga-toxigenic Escherichia coli (STEC). SubAB cleaves the molecular chaperone BiP/GRP78 in the endoplasmic reticulum (ER), leading to activation of RNA-dependent protein kinase (PKR)-like ER kinase (PERK), followed by caspase-dependent cell death. However, the SubAB uptake mechanism in HeLa cells is unknown. In this study, a variety of inhibitors and siRNAs were employed to characterize the SubAB uptake proces  ...[more]

Similar Datasets

| S-EPMC5841432 | biostudies-literature
| S-EPMC179786 | biostudies-literature
| S-EPMC1828409 | biostudies-literature
| S-EPMC9751135 | biostudies-literature
| S-EPMC2213318 | biostudies-literature
| S-EPMC5553146 | biostudies-other
| S-EPMC3852854 | biostudies-literature
| S-EPMC4807499 | biostudies-literature
| S-EPMC8263744 | biostudies-literature