Cannabinoid receptor 2 mediates the retention of immature B cells in bone marrow sinusoids

被引:169
作者
Pereira, Joao P. [1 ,2 ]
An, Jinping [1 ,2 ]
Xu, Ying [1 ,2 ]
Huang, Yong [3 ]
Cyster, Jason G. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Drug Studies Unit, Dept Biopharmaceut Sci, San Francisco, CA USA
关键词
IN-VIVO PERFUSION; ADHESION MOLECULE-1; CHEMOKINE SDF-1; STEM-CELLS; LYMPHOCYTE; EXPRESSION; BETA-1-INTEGRIN; CXCR4; RESPONSIVENESS; LOCALIZATION;
D O I
10.1038/ni.1710
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Immature B cells developing in the bone marrow are found in the parenchyma and sinusoids. The mechanisms that control the positioning of B cells in the sinusoids are not understood. Here we show that the integrin alpha(4)beta(1) (VLA-4) and its ligand VCAM-1 were required, whereas the chemokine receptor CXCR4 was dispensable, for sinusoidal retention of B cells. Instead, cannabinoid receptor 2 (CB2), a G alpha(i) protein-coupled receptor upregulated in immature B cells, was required for sinusoidal retention. Using two-photon microscopy, we found immature B cells entering and crawling in sinusoids; these immature B cells were displaced by CB2 antagonism. Moreover, CB2-deficient mice had a lower frequency of immunoglobulin lambda-chain-positive B cells in the peripheral blood and spleen. Our findings identify unique requirements for the retention of B cells in the bone marrow sinusoidal niche and suggest involvement of CB2 in the generation of the B cell repertoire.
引用
收藏
页码:403 / 411
页数:9
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