Cutting edge:: Differential roles for phosphoinositide 3-kinases, p110γ and p110δ, in lymphocyte chemotaxis and homing

被引:190
作者
Reif, K
Okkenhaug, K
Sasaki, T
Penninger, JM
Vanhaesebroeck, B
Cyster, JG
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[3] Babraham Inst, Mol Immunol Program, Cambridge, England
[4] Akita Univ, Sch Med & Precursory Res Empbryon Sci & Technol, 21st Century Ctr, Excellence Program, Akita 010, Japan
[5] Austrian Acad Sci, Inst Mol Biotechnol, A-1010 Vienna, Austria
[6] Univ Coll, Cell Signalling Grp, Ludwig Inst Canc Res, London, England
[7] Univ Coll, Dept Biochem & Mol Biol, London, England
关键词
D O I
10.4049/jimmunol.173.4.2236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite the established role for PI3Ks in cell migration, the PI3Ks involved in lymphocyte chemotaxis are poorly defined. In this study, we report that p110gamma-deficient T cells, but not B cells, show reduced chemotactic responses to the lymphoid chemokines, CCL19, CCL21, and CXCL12. As B cell and T cell chemotactic responses were both sensitive to the general PI3K inhibitors, wortmannin (WMN) and LY294002, we explored whether B cell responses were affected in mice lacking p110delta, a major PI3K isoform in lymphocytes. B cells deficient in p110delta showed diminished chemotactic responses, especially to CYCL13. Adoptive transfer experiments with WMN-treated wild-type B cells and with p110delta-deficient B cells revealed diminished homing to Peyer's patches and splenic white pulp cords. WMN selectively inhibited CXCR5-dependent B cell homing to Peyer's patches. These observations establish that p110gamma and p110delta function in lymphocyte chemotaxis, and show differential roles for PI3K family members in Band T cell migration.
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收藏
页码:2236 / 2240
页数:5
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