2010
DOI: 10.4161/epi.5.8.13106
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Differential epithelial cell response upon stimulation with theAggregatibacter actinomycetemcomitansstrains VT 1169, VT 1560 DAM-and ATCC 4318

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Cited by 3 publications
(2 citation statements)
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“…Interestingly, in gingival epithelial cells and gingival fibroblasts, the expression of human beta‐defensin‐2 and human beta‐defensin‐3 [also macrophage inflammatory protein‐2 alpha/chemokine (C‐C motif) ligand 20] genes was further up‐regulated when cells were exposed S. gordonii before stimulation with P. gingivalis . Even epigenetic variations in the bacterial DNA may influence the capacity of bacteria to stimulate the expression of antimicrobial peptides in gingival epithelial cells .…”
Section: Beta‐defensinsmentioning
confidence: 99%
“…Interestingly, in gingival epithelial cells and gingival fibroblasts, the expression of human beta‐defensin‐2 and human beta‐defensin‐3 [also macrophage inflammatory protein‐2 alpha/chemokine (C‐C motif) ligand 20] genes was further up‐regulated when cells were exposed S. gordonii before stimulation with P. gingivalis . Even epigenetic variations in the bacterial DNA may influence the capacity of bacteria to stimulate the expression of antimicrobial peptides in gingival epithelial cells .…”
Section: Beta‐defensinsmentioning
confidence: 99%
“…This attenuated phenotype was suggested to be due to its lacking bacterial DNAadenine-methyltransferase activity. Furthermore, the same study demonstrated that the observed effect in the innate immune response was perhaps associated with the heterogeneity of the studied human epithelial cells since the cells derived from different donors responded in a different manner (Eberhard et al 2010). These findings emphasize the potential significance of epigenetic modifications in the host microbial pathogenesis.…”
Section: Epigenetic Status In Infection-driven Inflammationmentioning
confidence: 73%