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10.1371/journal.ppat.1002341 http://scihub22266oqcxt.onion/10.1371/journal.ppat.1002341 C3207886!3207886 !22072963     free     free     free Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\22072963 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       PLoS+Pathog 2011 ; 7 (11 ): e1002341 Nephropedia Template TP {{tp|p=22072963 |t=2011. The critical role of Notch ligand Delta-like 1 in the pathogenesis of influenza A virus (H1N1) infection |pdf=|usr=}}{{22072963 }} gab.com Text The critical role of Notch ligand Delta-like 1 in the pathogenesis of influenza A virus (H1N1) infection JO: PLoS Pathog http://www.kidney.de/pget.php?&tw=1&pmid=22072963 #FOAvip Influenza A viral infections have been identified as the etiologic agents for historic pandemics, and contribute to the annual mortality associated with acute viral pneumonia. While both innate and acquired immunity are important in combating influenza virus infection, the mechanism connecting these arms of the immune system remains unknown. Recent data have indicated that the Notch system is an important bridge between antigen-presenting cells (APCs) and T cell communication circuits and plays a central role in driving the immune system to overcome disease. In the present study, we examine the role of Notch signaling during influenza H1N1 virus infection, focusing on APCs. We demonstrate here that macrophages, but not dendritic cells (DCs), increased Notch ligand Delta-like 1 (Dll1) expression following influenza virus challenge. Dll1 expression on macrophages was dependent on retinoic acid-inducible gene-I (RIG-I) induced type-I IFN pathway, and not on the TLR3-TRIF pathway. We also found that IFN?-Receptor knockout mice failed to induce Dll1 expression on lung macrophages and had enhanced mortality during influenza virus infection. Our results further showed that specific neutralization of Dll1 during influenza virus challenge induced higher mortality, impaired viral clearance, and decreased levels of IFN-?. In addition, we blocked Notch signaling by using ?-secretase inhibitor (GSI), a Notch signaling inhibitor. Intranasal administration of GSI during influenza infection also led to higher mortality, and higher virus load with excessive inflammation and an impaired production of IFN-? in lungs. Moreover, Dll1 expression on macrophages specifically regulates IFN-? levels from CD4(+)and CD8(+)T cells, which are important for anti-viral immunity. Together, the results of this study show that Dll1 positively influences the development of anti-viral immunity, and may provide mechanistic approaches for modifying and controlling the immune response against influenza H1N1 virus infection. Twit Text FOAVip The critical role of Notch ligand Delta-like 1 in the pathogenesis of influenza A virus (H1N1) infection ????PLoS Pathog http://www.kidney.de/pget.php?&tw=1&pmid=22072963 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=22072963 #FOAvip English Wikipedia <ref>{{Cite pmid|22072963 }}</ref> The critical role of Notch ligand Delta-like 1 in the pathogenesis of influenza A virus (H1N1) infection #MMPMID22072963 Ito T ; Allen RM ; Carson WF 4th ; Schaller M ; Cavassani KA ; Hogaboam CM ; Lukacs NW ; Matsukawa A ; Kunkel SL PLoS Pathog 2011[Nov]; 7 (11 ): e1002341 PMID22072963 show ga Influenza A viral infections have been identified as the etiologic agents for historic pandemics, and contribute to the annual mortality associated with acute viral pneumonia. While both innate and acquired immunity are important in combating influenza virus infection, the mechanism connecting these arms of the immune system remains unknown. Recent data have indicated that the Notch system is an important bridge between antigen-presenting cells (APCs) and T cell communication circuits and plays a central role in driving the immune system to overcome disease. In the present study, we examine the role of Notch signaling during influenza H1N1 virus infection, focusing on APCs. We demonstrate here that macrophages, but not dendritic cells (DCs), increased Notch ligand Delta-like 1 (Dll1) expression following influenza virus challenge. Dll1 expression on macrophages was dependent on retinoic acid-inducible gene-I (RIG-I) induced type-I IFN pathway, and not on the TLR3-TRIF pathway. We also found that IFN?-Receptor knockout mice failed to induce Dll1 expression on lung macrophages and had enhanced mortality during influenza virus infection. Our results further showed that specific neutralization of Dll1 during influenza virus challenge induced higher mortality, impaired viral clearance, and decreased levels of IFN-?. In addition, we blocked Notch signaling by using ?-secretase inhibitor (GSI), a Notch signaling inhibitor. Intranasal administration of GSI during influenza infection also led to higher mortality, and higher virus load with excessive inflammation and an impaired production of IFN-? in lungs. Moreover, Dll1 expression on macrophages specifically regulates IFN-? levels from CD4(+)and CD8(+)T cells, which are important for anti-viral immunity. Together, the results of this study show that Dll1 positively influences the development of anti-viral immunity, and may provide mechanistic approaches for modifying and controlling the immune response against influenza H1N1 virus infection. |Animals [MESH] |Antigen-Presenting Cells/immunology [MESH] |CD4-Positive T-Lymphocytes/immunology [MESH] |CD8-Positive T-Lymphocytes/immunology [MESH] |Calcium-Binding Proteins [MESH] |DEAD Box Protein 58 [MESH] |DEAD-box RNA Helicases/metabolism [MESH] |Dendritic Cells/immunology/metabolism [MESH] |Humans [MESH] |Influenza A Virus, H1N1 Subtype/*immunology/*pathogenicity [MESH] |Intercellular Signaling Peptides and Proteins/biosynthesis/*metabolism [MESH] |Interferon-alpha/genetics/immunology [MESH] |Interferon-gamma/immunology/metabolism [MESH] |Macrophages/immunology/*metabolism [MESH] |Mice [MESH] |Mice, Inbred C57BL [MESH] |Mice, Knockout [MESH] |Orthomyxoviridae Infections/*immunology/metabolism/virology [MESH] |Receptors, Notch/*metabolism [MESH]The critical role of Notch ligand Delta-like 1 in the pathogenesis of (epmc).pdf DeepDyve Pubget Overpricing