T cell-to-T cell clustering enhances NF-脙脙脙脙B activity by a PI3K signal mediated by Cbl-b and Rho
- 作者：Herndon ; Thomas M. ; Pirone ; Dana M. ; Tsokos ; George C. ; Chen ; Christopher S.
- 刊名：Biochemical and Biophysical Research Communications
- 出版年：2005
- 期刊代码：159_0006291x
- 类别：bio
- 出版时间：July 15, 2005
- 卷：332
- 期：4
- 页码：1133-1139
- 文件大小：708 K
摘要
Full activation of T cells requires the binding of antigen to the T cell receptor and stimulation of the CD28 molecule, a process which typically occurs when T cells bind to an antigen presenting cell. The transcription factor, NF-κB, is an integration point for these two signals and its activation is critical for T cell function. Using antibodies to the TCR and CD28 molecules to activate Jurkat T cells, we show that cells that were permitted to aggregate into multi-cellular clusters increased NF-κB activity compared to unclustered cells. Inhibition of PI3K signaling with wortmannin decreased the clustering-mediated NF-κB signal. Over-expression of a dominant negative form of Cbl-b, an endogenous inhibitor of PI3K, in unclustered cells rescued NF-κB activation to the same levels caused by cell clustering. Inhibiting signaling through Rho with dominant negative RhoA abrogated both clustering-mediated and dominant negative Cbl-b-mediated NF-κB inactivation, but not TCR/CD28 mediated NF-κB activation. Taken together, these results suggest that in addition to pathways stimulated by classical T cell–APC interactions, another signal arising from T cell clustering can enhance activation.