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Novel mutant mouse line emphasizes the importance of protein kinase C theta for CD4+ T lymphocyte activation

机译:新型突变小鼠系强调蛋白激酶C theta对CD4 + T淋巴细胞活化的重要性

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摘要

BackgroundThe protein kinase C theta (PKCθ) has an important and non-redundant function downstream of the antigen receptor and co-receptor complex in T lymphocytes. PKCθ is not only essential for activation of NF-κB, AP-1 and NFAT and subsequent interleukin-2 expression, but also critical for positive selection and development of regulatory T lymphocytes in the thymus. Several domains regulate its activity, such as a pseudosubstrate sequence mediating an auto-inhibitory intramolecular interaction, the tandem C1 domains binding diacylglycerol, and phosphorylation at conserved tyrosine, threonine as well as serine residues throughout the whole length of the protein. To address the importance of the variable domain V1 at the very N-terminus, which is encoded by exon 2, a mutated version of PKCθ was analyzed for its ability to stimulate T lymphocyte activation.
机译:背景技术蛋白激酶C theta(PKCθ)在T淋巴细胞的抗原受体和共受体复合物下游具有重要且非冗余的功能。 PKCθ不仅对于激活NF-κB,AP-1和NFAT以及随后的白介素2表达必不可少,而且对于在胸腺中阳性选择和调节性T淋巴细胞的发育也至关重要。多个结构域调节其活性,例如介导自抑制性分子内相互作用的伪底物序列,结合二酰基甘油的串联C1域以及在整个蛋白全长上保守的酪氨酸,苏氨酸和丝氨酸残基的磷酸化。为了解决可变结构域V1在外显子2编码的N端的重要性,分析了突变形式的PKCθ刺激T淋巴细胞活化的能力。

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