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  • 标题:Cdc42 interacting protein 4 (CIP4) is essential for integrin-dependent T-cell trafficking
  • 本地全文:下载
  • 作者:Suresh Koduru ; Lalit Kumar ; Michel J. Massaad
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2010
  • 卷号:107
  • 期号:37
  • 页码:16252-16256
  • DOI:10.1073/pnas.1002747107
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:The F-BAR domain containing protein CIP4 (Cdc42 interacting protein 4) interacts with Cdc42 and WASP/N-WASP and is thought to participate in the assembly of filamentous actin. CIP4-/- mice had normal T- and B-lymphocyte development but impaired T cell-dependent antibody production, IgG antibody affinity maturation, and germinal center (GC) formation, despite an intact CD40L-CD40 axis. CIP4-/- mice also had impaired contact hypersensitivity (CHS) to haptens, and their T cells failed to adoptively transfer CHS. Ovalbumin-activated CD4+ effector T cells from CIP4-/-/OT-II mice migrated poorly to antigen-challenged skin. Activated CIP4-/- T cells exhibited impaired adhesion and polarization on immobilized VCAM-1 and ICAM-1 and defective arrest and transmigration across murine endothelial cell monolayers under shear flow conditions. These results demonstrate an important role for CIP4 in integrin-dependent T cell-dependent antibody responses and GC formation and in integrin-mediated recruitment of effector T cells to cutaneous sites of antigen-driven immune reactions.
  • 关键词:F-BAR ; inflammation ; contact hypersensitivity ; antigen response ; adhesion
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