The tetraspanin CD81 is necessary for partitioning of coligated CD19/CD21-B cell antigen receptor complexes into signaling-active lipid rafts

被引:115
作者
Cherukuri, A
Shoham, T
Sohn, HW
Levy, S
Brooks, S
Carter, R
Pierce, SK
机构
[1] NIAID, Immunogenet Lab, NIH, Rockville, MD 20852 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Oncol, Stanford, CA 94305 USA
[3] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
[4] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
关键词
D O I
10.4049/jimmunol.172.1.370
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tetraspanins have been hypothesized to facilitate the organization of functional multimolecular membrane complexes. In B cells the tetraspanin CD81 is a component of the CD19/CD21 complex. When coligated to the B cell Ag receptor (BCR), the CD19/CD21 complex significantly enhances BCR signaling in part by prolonging the association of the BCR with signaling-active lipid rafts. In this study CD81 is shown to associate with lipid rafts upon coligation of the BCR and the CD19/CD21 complex. Using B cells from CD81-deficient mice we demonstrate that in the absence of CD81, coligated BCR and CD19/CD21 complexes fail to partition into lipid rafts and enhance BCR signaling from rafts. Furthermore, a chimeric CD19 protein that associates only weakly if at all with CD81 fails to promote the association of coligated BCR with lipid rafts. The requirement for CD81 to promote lipid raft association may define a novel mechanism by which tetraspanins function as molecular facilitators of signaling receptors.
引用
收藏
页码:370 / 380
页数:11
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