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https://irlib.pccu.edu.tw/handle/987654321/26761
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題名: | Glutamine modulates CD8 alpha alpha(+) TCR alpha beta(+) intestinal intraepithelial lymphocyte expression in mice with polymicrobial sepsis |
作者: | Tung, JN (Tung, Jai-Nien) Lee, WY (Lee, Wan-Yun) Pai, MH (Pai, Man-Hui) Chen, WJ (Chen, Wei-Jao) Yeh, CL (Yeh, Chiu-Li) Yeh, SL (Yeh, Sung-Ling) |
貢獻者: | Dept Food & Nutr |
關鍵詞: | Sepsis;Glutamine Intraepithelial lymphocytes CD8 alpha alpha(+) TCR alpha beta(+) IELs Apoptosis |
日期: | 2013-06 |
上傳時間: | 2014-02-25 14:52:27 (UTC+8) |
摘要: | Objectives: CD8 alpha alpha(+) T-cell receptor (TCR) alpha beta(+) intestinal intraepithelial lymphocytes (IELs) were found to have a regulatory function in the mucosa] immune system. Glutamine (GLN) is an amino acid with immunomodulatory effects. The aim of this study was to investigate the influences of GLN on the proportion of CD8 alpha alpha(+) TCR alpha beta(+) IELs and associated inflammatory mediator gene expression in polymicrobial sepsis.
Methods: Mice were randomly assigned to a normal (NC) group, a sepsis with saline (SS) group, or a sepsis with GLN (SG) group. The NC group was fed a chow diet. Sepsis was induced by cecal ligation and puncture (CLP). The SS group was administered saline, and the SG group was given 0.75 g GLN/kg body weight via a tail vein after CLP. Mice were sacrificed 12 h after CLP, and CD8 alpha alpha(+) TCR alpha beta(+) IELs were isolated for further analysis.
Results: Sepsis resulted in a lower percentage of CDS alpha alpha(+) TCR alpha beta(+) IELs, and higher messenger (m)RNA expression of complement 5a receptor, interleukin (IL)-2 receptor beta, IL-15 receptor alpha, and interferon-gamma by CD8 alpha alpha(+) TCR alpha beta(+) IELs. These immunomodulatory mediator genes decreased, whereas IL-7 receptor and transforming growth factor-beta expressions increased in CD8 alpha alpha(+) TCR alpha beta(+) IELs in septic mice with GLN administration. Annexin V/7-AAD staining revealed significantly lower apoptotic rates of CD8 alpha alpha(+) TCR alpha beta(+) IELs in the SG group.
Conclusion: A single dose of GLN administered after the initiation of sepsis increased the percentage of CD8 alpha alpha(+) TCR alpha beta(+) IELs, prevented apoptosis of CD8 alpha alpha(+) TCR alpha beta(+) IELs, and downregulated CD8 alpha alpha(+) TCR alpha beta(+) IEL-expressed inflammatory mediators. These results suggest that GLN influenced the distribution and cytokine secretion of the CD8 alpha alpha(+) TCR alpha beta(+) IEL subset, which may ameliorate sepsis-induced inflammatory reactions and thus mitigate the severity of intestinal epithelial injury. (C) 2013 Elsevier Inc. All rights reserved. |
關聯: | NUTRITION Volume: 29 Issue: 6 Pages: 911-917 |
顯示於類別: | [保健營養學系 ] 期刊論文
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