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  • 标题:Development of TCRαβ CD8αα Intestinal Intraepithelial Lymphocytes Is Promoted by Interleukin-15-Producing Epithelial Cells Constitutively Stimulated by Gram-Negative Bacteria via TLR4
  • 本地全文:下载
  • 作者:Masahiro Kaneko ; Tsunehide Mizunuma ; Hiroaki Takimoto
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2004
  • 卷号:27
  • 期号:6
  • 页码:883-889
  • DOI:10.1248/bpb.27.883
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:The microbes present in the intestine have a strong influence on the development and maturation of lymphoid organs. The cross-talk mechanisms between intestinal intraepithelial lymphocytes (i-IEL) and noninvasive microbes are still poorly understood. The influence of microbes and lipopolysaccharides on the development of i-IEL, especially the TCRαβ+ CD8αα subset, was investigated using the different TLR4-mutant mouse strains C3H/HeJ, BALB/lpsd, and C57BL/10ScCr. Intestinal epithelial cells (i-EC) from TLR4-mutant strains did not express interleukin (IL)-15 mRNA, while IL-15 mRNA expression in i-EC from the corresponding wild-type, C3H/He, BALB/c, and C57BL/10ScSn mice was detected. The development of TCRαβ+ CD8αα cells in i-IEL significantly decreased in TLR4-mutant mice compared with the corresponding wild-type mice, while other T cell subsets in i-IEL showed similar percentages in the TLR4-mutant and wild-type mice. Adult thymectomized (ATx-) and lethally irradiated C3H/HeJ mice reconstituted with T cell-depleted bone marrow cells from C3H/He mice showed a significantly lower percentage of TCRαβ CD8αα i-IEL than ATx-C3H/He mice after transfer of C3H/HeJ BM cells. The percentage of TCRαβ CD8αα i-IEL and IL-15 mRNA expression in i-EC from BALB/lpsd mice did not increase during Salmonella typhimurium infection but was significantly enhanced during Listeria monocytogenes infection. Our findings suggest that LPS induces IL-15 production by i-EC, resulting in the development of TCRαβ CD8αα i-IEL.
  • 关键词:intestinal intraepithelial lymphocyte;TCRαβ CD8αα;interleukin-15;TLR4;intestinal epithelial cell
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