Triacyl-lipopentapeptide adjuvants:: TLR2-dependent activation of macrophages and modulation of receptor-mediated cell activation by altering acyl-moieties

被引:16
作者
Müller, SDC
Müller, MR
Huber, M
Esche, UVD
Kirschning, CJ
Wagner, H
Bessler, WG
Mittenbühler, K
机构
[1] Univ Freiburg, Inst Mol Med & Zellforsch, D-79104 Freiburg, Germany
[2] Tech Univ Munich, Inst Med Mikrobiol Immunol & Hyg, D-81675 Munich, Germany
关键词
monocytes/macrophages; cellular activation; protein kinases; biochemistry; immunochemistry;
D O I
10.1016/j.intimp.2004.04.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Synthetic lipopeptides derived from bacterial lipoprotein are efficient immumoadjuvants. In vitro they activate antigen presenting cells (APCs) to induce the translocation of nuclear factor kappa B (NF-kappaB) and the activation of further transcription factors. This results in the expression of genes encoding cytokines such as IL-1, IL-6, TNF-alpha and in the release of reactive oxygen/nitrogen intermediates. The molecular structure of microbial products determines TLR specificity and thus their activatory potential and immunoadjuvanticity. In the present study, we investigated the lipopeptide-induced activation of leukocytes at different cellular levels by applying derivatives of a synthetic lipopentapeptide-fatty acid library. Our results show that TLR2 plays a key role for the activation of bone marrow-derived macrophages (BMDMs) by lipopentapeptide derivatives and that the fatty acid composition of the lipopeptides determines their activation potential and TLR specificity. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1287 / 1300
页数:14
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