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Soluble Egg Antigen Activates M2 Macrophages via the STAT6 and PI3K Pathways, and Schistosoma Japonicum Alternatively Activates Macrophage Polarization to Improve the Survival Rate of Septic Mice.
Tang, Hao; Liang, Yan-Bing; Chen, Zhi-Bin; Du, Lin-Lin; Zeng, Li-Jin; Wu, Jing-Guo; Yang, Wen; Liang, Hua-Ping; Ma, Zhong-Fu.
Afiliação
  • Tang H; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Liang YB; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Chen ZB; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Du LL; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Zeng LJ; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Wu JG; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Yang W; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
  • Liang HP; The Third Military Medical University, Chongqing, 400038, China.
  • Ma ZF; Department of General Internal Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
J Cell Biochem ; 118(12): 4230-4239, 2017 12.
Article em En | MEDLINE | ID: mdl-28419526
Sepsis is one of the most challenging health problems worldwide. Our previous study showed that chronic schistosoma japonica (SJ) infection might increase serum anti-inflammatory factors to play a protective role, thus improving the survival rate of septic mice. Further research revealed that SJ infection promoted J774A.1 macrophage differentiation into M2 macrophages; suppressed LPS-induced activation of M1 macrophages; up-regulated CD163, IL-10, and TGF-ß1 expression; inhibited TNF-α and iNOS expression; and blocked the effect of LPS-promoted TNF-α and iNOS expression. Furthermore, adoptive transfer of ex vivo programed M2 macrophages significantly increased the survival rate of septic mice. In vitro studies suggested that soluble egg antigen (SEA) from SJ played the same role as worm infection but had no impact on M1 macrophages. SEA reduced LPS-induced TNF-α and iNOS expression, decreased the inhibitory effect of LPS on IL-10 and TGF-ß1 expression, increased STAT6 phosphorylation, and up-regulated PI3K and Akt expression but inhibited SOCS1 expression. When PI3K inhibitors were added, SEA-induced expression of CD163, IL-10, and arg1 might be reduced. Therefore, worm infection has a protective effect in septic mice in which SEA may play a key role via the STAT6 and PI3K pathways. This finding may provide a favorable solution for the treatment of sepsis, especially early cases. J. Cell. Biochem. 118: 4230-4239, 2017. © 2017 Wiley Periodicals, Inc.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquistossomose Japônica / Transdução de Sinais / Citocinas / Sepse / Macrófagos / Antígenos de Helmintos Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquistossomose Japônica / Transdução de Sinais / Citocinas / Sepse / Macrófagos / Antígenos de Helmintos Idioma: En Ano de publicação: 2017 Tipo de documento: Article