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. 2019 Mar 25;76(12):2383–2389. doi: 10.1007/s00018-019-03076-7

Table 1.

Signals and biological functions involved in crosstalk between bacteria and mammalian hosts

Prokaryotic signals Eukaryotic cell Eukaryotic function References Eukaryotic signals Prokaryotic function References
3O-C12-HSL Skin cells Stimulates the expression of cytokines including IL-1α and IL-6 [29] α-Defensin Controls bacterial localization [48]
3O-C12-HSL Macrophage, B cells, T cells, spleen cells Modulates cell activities and antibody responses [40] Bile acid Affects AI activity [49]
3O-C12-HSL Lymphocytes Inhibits cytokine production and lymphocyte proliferation [41, 42] Paraoxonases Degrading AIs [50, 51]
3O-C12-HSL BM-DCs Decreases the ability of BM-DCs to induce T-cell proliferation and activation [43, 44] AI-2 mimics Affect gene expression of bacteria [26]
3O-C12-HSL Macrophages, neutrophils Cytotoxicity [38] Noradrenaline Promotes bacterial growth [54]
3O-C12-HSL BM-DMs Disruption of NF-kB signaling [45] Epinephrine Mimic the activity of AI-3 [56]
AI-2 Colon cancer cells Regulates Interleukin-8 expression [28] Dynorphin Activates QS signaling and enhanced bacterial virulence [57]
AI-2 Pneumocytes Cellular damage [31]
DPD Gingival epithelial cells Enhances cell proliferation [27]
AI peptides Colon cancer cells Tumor metastasis [46]
AI-3 HeLa cells Produces AE lesions [56]

AE attaching and effacing, AI autoinducer, BM-DCs bone marrow-derived dendritic cells, BM-DMs bone marrow-derived macrophages, DPD dihydroxy-2,3-pentanedione (precursor of AI-2), QS quorum sensing