2014
DOI: 10.1128/iai.01980-14
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Aggregatibacter actinomycetemcomitans Outer Membrane Vesicles Are Internalized in Human Host Cells and Trigger NOD1- and NOD2-Dependent NF-κB Activation

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Cited by 114 publications
(115 citation statements)
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“…69). Similarly, A. actinomycetemcomitans OMVs induce NOD1-and NOD2-dependent responses in HEK293 cells and NOD1-driven inflammation in THP-1 myeloid cells 71 . Furthermore, V. cholerae OMVs induce NOD1-dependent production of CCL2 and CCL20 by epithelial cells 70 .…”
Section: Engagement Of Intracellular Prrsmentioning
confidence: 99%
“…69). Similarly, A. actinomycetemcomitans OMVs induce NOD1-and NOD2-dependent responses in HEK293 cells and NOD1-driven inflammation in THP-1 myeloid cells 71 . Furthermore, V. cholerae OMVs induce NOD1-dependent production of CCL2 and CCL20 by epithelial cells 70 .…”
Section: Engagement Of Intracellular Prrsmentioning
confidence: 99%
“…While the subcellular localization and expression of NOD1 and NOD2 vary depending on the cell type, the source and route of entry of the ligand also influence NOD1 and NOD2 complex formation. Indeed, outer membrane vesicles (OMVs) from a variety of bacteria (Irving et al, 2014; Thay et al, 2014) activate NOD1 and NOD2 signaling revealing an important role for vesicle internalization in the delivery of ligands to cytosolic NOD1 and NOD2 receptors. Given that soluble NOD1 and NOD2 ligands are sufficient to stimulate host cells there are clearly multiple routes for these molecules to enter the cell.…”
Section: Nod1 and Nod2: Ligand Recognition And Activationmentioning
confidence: 99%
“…Other PRRs that respond to extracellular bacteria are localized in the cytosol, but their discovery prompted the question of how and why bacterial products translocate to the host cell cytosol. An explanation was provided by the demonstration that MVs produced by Helicobacter pylori, Pseudomonas aeruginosa, Neisseria gonorrhea, and Aggregatibacter actinomycetemcomitans contain peptidoglycan, fuse with host cell membranes, and activate NOD1/NOD2 (Kaparakis et al, 2010; Thay et al, 2014). More recently, it was demonstrated that enterohemorrhagic E. coli MVs traffic LPS to the cytosol of host cells and activate non-canonical inflammasome signaling (Vanaja et al, 2016).…”
Section: Immune Modulation By Bacterial Membrane Vesiclesmentioning
confidence: 99%