Phosphatidylinositol mannosides: Synthesis and suppression of allergic airway disease

被引:38
作者
Ainge, Gary D.
Hudson, Jennifer
Larsen, David S.
Painter, Gavin F.
Gill, Gurmit Singh
Harper, Jacquie L.
机构
[1] Univ Otago, Dunedin, New Zealand
[2] Ind Res Ltd, Lower Hutt, New Zealand
[3] Malaghan Inst Med Res, Wellington, New Zealand
关键词
phosphatidylinositol mannans; PIMs; asthma; inflammation;
D O I
10.1016/j.bmc.2006.04.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Phosphatidylinositol mannoside (PIM) extracts from mycobacteria have been shown previously to suppress allergic airway inflammation in mice. To help determine the structural requirements for activity, PIM1(2) (1), PIM1(6) (2) and PIM2 (3) were synthesized and tested for their ability to suppress cellular inflammation in a mouse model of allergic asthma. The synthetic PIMs were all effective in suppressing airway eosinophilia in the asthma model, with PIM16 being the most effective. Suppression of all inflammatory cells monitored was observed, indicating a general blockade of cellular inflammation. Non-mannosylated phosphatidylinositol (PI) had no suppressive effect, indicating that at least one alpha-D-mannopyranosyl residue is necessary for activity. The suppressive effect of the three PIM compounds indicates that other members of this set may be of value in treatment of a range of diseases driven by infiltration of inflammatory cells. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5632 / 5642
页数:11
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