Receptor-Independent, Direct Membrane Binding Leads to Cell-Surface Lipid Sorting and Syk Kinase Activation in Dendritic Cells

被引:219
作者
Ng, Gilbert [1 ]
Sharma, Karan [1 ]
Ward, Sandra M. [2 ]
Desrosiers, Melanie D. [1 ]
Stephens, Leslie A. [1 ]
Schoel, W. Michael [3 ]
Li, Tonglei [4 ]
Lowell, Clifford A. [5 ,6 ]
Ling, Chang-Chun [2 ]
Amrein, Matthias W. [3 ]
Shi, Yan [1 ]
机构
[1] Univ Calgary, Dept Microbiol & Infect Dis, Immunol Res Grp, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Dept Chem, Immunol Res Grp, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Dept Biol & Anat, Immunol Res Grp, Calgary, AB T2N 4N1, Canada
[4] Univ Kentucky, Dept Pharmaceut Sci, Lexington, KY 40536 USA
[5] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.immuni.2008.09.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Binding of particulate antigens by antigen-presenting cells is a critical step in immune activation. Previously, we demonstrated that uric acid crystals are potent adjuvants, initiating a robust adaptive immune response. However, the mechanisms of activation are unknown. By using atomic force microscopy as a tool for real-time single-cell activation analysis, we report that uric acid crystals could directly engage cellular membranes, particularly the cholesterol components, with a force substantially stronger than protein-based cellular contacts. Binding of particulate substances activated Syk kinase-dependent signaling in dendritic cells. These observations suggest a mechanism whereby immune cell activation can be triggered by solid structures via membrane lipid alteration without the requirement for specific cell-surface receptors, and a testable hypothesis for crystal-associated arthropathies, inflammation, and adjuvanticity.
引用
收藏
页码:807 / 818
页数:12
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