Ellis J H, Sutmuller R P, Sims M J, Cooksley S
Immunopathology Unit, Glaxo Wellcome, Medicines Research Centre, Gunnels Wood Road, Stevenage, Herts. SG1 2NY, UK.
Biochem J. 1998 Oct 15;335 ( Pt 2)(Pt 2):277-84. doi: 10.1042/bj3350277.
T lymphocytes express a range of tyrosine kinases that are involved in signalling processes driving cell activation, proliferation and differentation. Two tyrosine kinases expressed only in T cells, the Itk/Emt and Txk gene products, are members of the Tec family of kinases. The role of Tec kinases in cellular function is poorly understood, although a Tec kinase specific to B cells, Btk, is essential for B-cell development. To explore the contribution of the T-cell-specific Tec kinases to lymphocyte function, we have expressed human Txk in the baculovirus system and conducted the first characterization of its activity. We find that Txk exhibits a substrate preference in vitro quite distinct from that of the major T-cell kinases Lck and ZAP70, suggesting that Tec-family kinases might act on a distinct range of substrates. We also investigated the interactions of Txk with the cytoplasmic domains of the key signalling molecules CD3zeta, CD28 and CTLA4 and find that none of these are phosphorylated by Txk, nor are they ligands for the SH2 or SH3 domains of Txk. We conclude that it is unlikely that Txk has a role in the early signal transduction events associated with these key pathways controlling T-cell activation.
T淋巴细胞表达一系列酪氨酸激酶,这些激酶参与驱动细胞活化、增殖和分化的信号传导过程。仅在T细胞中表达的两种酪氨酸激酶,即Itk/Emt和Txk基因产物,是Tec激酶家族的成员。尽管B细胞特异性的Tec激酶Btk对B细胞发育至关重要,但Tec激酶在细胞功能中的作用仍知之甚少。为了探究T细胞特异性Tec激酶对淋巴细胞功能的贡献,我们在杆状病毒系统中表达了人Txk,并对其活性进行了首次表征。我们发现,Txk在体外表现出与主要的T细胞激酶Lck和ZAP70截然不同的底物偏好,这表明Tec家族激酶可能作用于不同范围的底物。我们还研究了Txk与关键信号分子CD3ζ、CD28和CTLA4的细胞质结构域之间的相互作用,发现这些分子均未被Txk磷酸化,也不是Txk的SH2或SH3结构域的配体。我们得出结论,Txk不太可能在与这些控制T细胞活化的关键途径相关的早期信号转导事件中发挥作用。