tetano
Editor, Senior Moderator
Cell Immunol. 2019 Jul 3:103949. doi: 10.1016/j.cellimm.2019.103949. [Epub ahead of print]
[h=1]Protease-activated receptor 4 protects mice from Coxsackievirus B3 and H1N1 influenza A virus infection.[/h] Tatsumi K[SUP]1[/SUP], Schmedes CM[SUP]1[/SUP], Houston ER[SUP]1[/SUP], Butler E[SUP]1[/SUP], Mackman N[SUP]1[/SUP], Antoniak S[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] PAR4 is expressed by a variety of cells, including platelets, cardiac, lung and immune cells. We investigated the contribution of PAR4 to viral infections of the heart and lung. Toll-like receptor (TLR) 3-dependent immune responses were analyzed after co-stimulation of PAR4 in murine bone-marrow derived macrophages, embryonic fibroblasts and embryonic cardiomyocytes. In addition, we analyzed Coxsackievirus B3 (CVB3) or H1N1 influenza A virus (H1N1 IAV) infection of PAR4[SUP]-/-[/SUP] (ΔPAR4) and wild-type (WT) mice. Lastly, we investigated the effect of platelet inhibition on H1N1 IAV infection. In vitro experiments revealed that PAR4 stimulation enhances the expression of TLR3-dependent CXCL10 expression and decreases TLR3-dependent NFκB-mediated proinflammatory gene expression. Furthermore, CVB3-infected ΔPAR4 mice exhibited a decreased anti-viral response and increased viral genomes in the heart leading to more pronounced CVB3 myocarditis compared to WT mice. Similarly, H1N1 IAV-infected ΔPAR4 mice had increased immune cell numbers and inflammatory mediators in the lung, and increased mortality compared with infected WT controls. The study showed that PAR4 protects mice from viral infections of the heart and lung.
Copyright ? 2019 Elsevier Inc. All rights reserved.
[h=4]KEYWORDS:[/h] Influenza; Innate immune responses; Myocarditis; Protease-activated receptor 4
PMID: 31337508 DOI: 10.1016/j.cellimm.2019.103949
[h=1]Protease-activated receptor 4 protects mice from Coxsackievirus B3 and H1N1 influenza A virus infection.[/h] Tatsumi K[SUP]1[/SUP], Schmedes CM[SUP]1[/SUP], Houston ER[SUP]1[/SUP], Butler E[SUP]1[/SUP], Mackman N[SUP]1[/SUP], Antoniak S[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] PAR4 is expressed by a variety of cells, including platelets, cardiac, lung and immune cells. We investigated the contribution of PAR4 to viral infections of the heart and lung. Toll-like receptor (TLR) 3-dependent immune responses were analyzed after co-stimulation of PAR4 in murine bone-marrow derived macrophages, embryonic fibroblasts and embryonic cardiomyocytes. In addition, we analyzed Coxsackievirus B3 (CVB3) or H1N1 influenza A virus (H1N1 IAV) infection of PAR4[SUP]-/-[/SUP] (ΔPAR4) and wild-type (WT) mice. Lastly, we investigated the effect of platelet inhibition on H1N1 IAV infection. In vitro experiments revealed that PAR4 stimulation enhances the expression of TLR3-dependent CXCL10 expression and decreases TLR3-dependent NFκB-mediated proinflammatory gene expression. Furthermore, CVB3-infected ΔPAR4 mice exhibited a decreased anti-viral response and increased viral genomes in the heart leading to more pronounced CVB3 myocarditis compared to WT mice. Similarly, H1N1 IAV-infected ΔPAR4 mice had increased immune cell numbers and inflammatory mediators in the lung, and increased mortality compared with infected WT controls. The study showed that PAR4 protects mice from viral infections of the heart and lung.
Copyright ? 2019 Elsevier Inc. All rights reserved.
[h=4]KEYWORDS:[/h] Influenza; Innate immune responses; Myocarditis; Protease-activated receptor 4
PMID: 31337508 DOI: 10.1016/j.cellimm.2019.103949