The Cytoskeletal Adaptor Protein IQGAP1 Regulates TCR-Mediated Signaling and Filamentous Actin Dynamics

被引:38
|
作者
Gorman, Jacquelyn A. [1 ]
Babich, Alexander [2 ,3 ]
Dick, Christopher J. [1 ]
Schoon, Renee A. [1 ]
Koenig, Alexander [4 ]
Gomez, Timothy S. [1 ,4 ]
Burkhardt, Janis K. [2 ,3 ]
Billadeau, Daniel D. [1 ,4 ]
机构
[1] Mayo Clin, Dept Immunol, Coll Med, Schulze Ctr Novel Therapeut, Rochester, MN 55905 USA
[2] Univ Penn, Dept Pathol & Lab Med, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Mayo Clin, Div Oncol Res, Schulze Ctr Novel Therapeut, Coll Med, Rochester, MN 55901 USA
来源
JOURNAL OF IMMUNOLOGY | 2012年 / 188卷 / 12期
基金
美国国家卫生研究院;
关键词
T-CELL-RECEPTOR; CALPONIN HOMOLOGY DOMAIN; RASGAP-RELATED PROTEIN; IMMUNOLOGICAL SYNAPSE; GRANULE EXOCYTOSIS; BINDING PROTEIN; ACTIVATION; COMPLEX; IDENTIFICATION; MIGRATION;
D O I
10.4049/jimmunol.1103487
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Ras GTPase-activating-like protein IQGAP1 is a multimodular scaffold that controls signaling and cytoskeletal regulation in fibroblasts and epithelial cells. However, the functional role of IQGAP1 in T cell development, activation, and cytoskeletal regulation has not been investigated. In this study, we show that IQGAP1 is dispensable for thymocyte development as well as microtubule organizing center polarization and cytolytic function in CD8(+) T cells. However, IQGAP1-deficient CD8(+) T cells as well as Jurkat T cells suppressed for IQGAP1 were hyperresponsive, displaying increased IL-2 and IFN-gamma production, heightened LCK activation, and augmented global phosphorylation kinetics after TCR ligation. In addition, IQGAP1-deficient T cells exhibited increased TCR-mediated F-actin assembly and amplified F-actin velocities during spreading. Moreover, we found that discrete regions of IQGAP1 regulated cellular activation and F-actin accumulation. Taken together, our data suggest that IQGAP1 acts as a dual negative regulator in T cells, limiting both TCR-mediated activation kinetics and F-actin dynamics via distinct mechanisms. The Journal of Immunology, 2012, 188: 6135-6144.
引用
收藏
页码:6135 / 6144
页数:10
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