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Int. J. Mol. Sci. 2013, 14(4), 7327-7340; doi:10.3390/ijms14047327
Article

A Role for Protein Phosphatase 2A in Regulating p38 Mitogen Activated Protein Kinase Activation and Tumor Necrosis Factor-Alpha Expression during Influenza Virus Infection

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Received: 13 December 2012; in revised form: 21 March 2013 / Accepted: 26 March 2013 / Published: 2 April 2013
(This article belongs to the Special Issue Advances in Molecular Immunology)
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Abstract: Influenza viruses of avian origin continue to pose pandemic threats to human health. Some of the H5N1 and H9N2 virus subtypes induce markedly elevated cytokine levels when compared with the seasonal H1N1 virus. We previously showed that H5N1/97 hyperinduces tumor necrosis factor (TNF)-alpha through p38 mitogen activated protein kinase (MAPK). However, the detailed mechanisms of p38MAPK activation and TNF-alpha hyperinduction following influenza virus infections are not known. Negative feedback regulations of cytokine expression play important roles in avoiding overwhelming production of proinflammatory cytokines. Here we hypothesize that protein phosphatases are involved in the regulation of cytokine expressions during influenza virus infection. We investigated the roles of protein phosphatases including MAPK phosphatase-1 (MKP-1) and protein phosphatase type 2A (PP2A) in modulating p38MAPK activation and downstream TNF-alpha expressions in primary human monocyte-derived macrophages (PBMac) infected with H9N2/G1 or H1N1 influenza virus. We demonstrate that H9N2/G1 virus activated p38MAPK and hyperinduced TNF-alpha production in PBMac when compared with H1N1 virus. H9N2/G1 induced PP2A activity in PBMac and, with the treatment of a PP2A inhibitor, p38MAPK phosphorylation and TNF-alpha production were further increased in the virus-infected macrophages. However, H9N2/G1 did not induce the expression of PP2A indicating that the activation of PP2A is not mediated by p38MAPK in virus-infected PBMac. On the other hand, PP2A may not be the targets of H9N2/G1 in the upstream of p38MAPK signaling pathways since H1N1 also induced PP2A activation in primary macrophages. Our results may provide new insights into the control of cytokine dysregulation.
Keywords: protein phosphatase 2A; tumor necrosis factor-alpha; p38 mitogen activated protein kinase; influenza virus protein phosphatase 2A; tumor necrosis factor-alpha; p38 mitogen activated protein kinase; influenza virus
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Law, A.H.Y.; Tam, A.H.M.; Lee, D.C.W.; Lau, A.S.Y. A Role for Protein Phosphatase 2A in Regulating p38 Mitogen Activated Protein Kinase Activation and Tumor Necrosis Factor-Alpha Expression during Influenza Virus Infection. Int. J. Mol. Sci. 2013, 14, 7327-7340.

AMA Style

Law AHY, Tam AHM, Lee DCW, Lau ASY. A Role for Protein Phosphatase 2A in Regulating p38 Mitogen Activated Protein Kinase Activation and Tumor Necrosis Factor-Alpha Expression during Influenza Virus Infection. International Journal of Molecular Sciences. 2013; 14(4):7327-7340.

Chicago/Turabian Style

Law, Anna H.Y.; Tam, Alex H.M.; Lee, Davy C.W.; Lau, Allan S.Y. 2013. "A Role for Protein Phosphatase 2A in Regulating p38 Mitogen Activated Protein Kinase Activation and Tumor Necrosis Factor-Alpha Expression during Influenza Virus Infection." Int. J. Mol. Sci. 14, no. 4: 7327-7340.



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