Uncoordinated 119 Protein Controls Trafficking of Lck via the Rab11 Endosome and Is Critical for Immunological Synapse Formation

被引:79
作者
Gorska, Magdalena M. [1 ,2 ,3 ]
Liang, Qiaoling [1 ]
Karim, Zunayet [1 ]
Anm, Rafeul [1 ,2 ,3 ]
机构
[1] Natl Jewish Hlth, Dept Med, Div Allergy & Immunol, Denver, CO 80206 USA
[2] Univ Colorado, Dept Med, Div Allergy & Immunol, Denver, CO 80206 USA
[3] Hlth Sci Ctr, Denver, CO 80206 USA
基金
美国国家卫生研究院;
关键词
HUMAN T-LYMPHOCYTES; PLASMA-MEMBRANE; TYROSINE KINASES; RECYCLING ENDOSOMES; ANTIGEN RECEPTOR; LIPID RAFTS; HRG4; UNC119; PATHWAY; CELLS; TCR;
D O I
10.4049/jimmunol.0900792
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 activation of T cells through the TCR is essential for development of the adaptive immune response. TCR does not have any enzymatic activity and relies on the plasma membrane-associated lymphocyte-specific protein tyrosine kinase (Lck) for initiation of signaling. Here we uncover a mechanism that is responsible for plasma membrane targeting of Lck. We show that Lck is transported to the membrane via a specific endosomal compartment. The transport depends on the adaptor protein Uncoordinated 119 (Unc119), on the GTPase rat brain 11 (Rab11), and on the actin cytoskeleton. Unc119 regulates the activation of Rab11. Consequently, Unc119 orchestrates the recruitment of the actin-based motor protein, myosin 513, and the organization of multiprotein complexes on endosomes. The Unc119-regulated pathway is essential for immunological synapse formation and T cell activation. The Journal of Immunology, 2009,,183: 1675-1684.
引用
收藏
页码:1675 / 1684
页数:10
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