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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >KIR2DL4 (CD158d), an NK Cell-Activating Receptor with Inhibitory Potential.
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KIR2DL4 (CD158d), an NK Cell-Activating Receptor with Inhibitory Potential.

机译:KIR2DL4(CD158d),具有抑制潜能的NK细胞激活受体。

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摘要

KIR2DL4 (CD158d) is an unusual member of the killer cell Ig-like receptor family expressed in all NK cells and some T cells. KIR2DL4 activates the cytotoxicity of NK cells, despite the presence of an immunoreceptor tyrosine-based inhibition motif (ITIM) in its cytoplasmic tail. The role of this ITIM on the activating function of KIR2DL4, and whether it can provide inhibitory signals, is not known. Mutated forms of KIR2DL4 were engineered that lacked either the tyrosine in the ITIM or an arginine-tyrosine motif in the transmembrane region that is required for the activation signal. The activity of the mutated KIR2DL4 molecules was tested in a redirected lysis assay. The ITIM was not necessary for activation of lysis by KIR2DL4. The activation signal of KIR2DL4 was sensitive to inhibition by another ITIM-containing receptor. The activation-deficient mutant of KIR2DL4 inhibited the signal delivered by the activating receptor CD16. In pull-down experiments with GST fusion proteins, the tyrosine-phosphorylated cytoplasmic tail of KIR2DL4 bound the Src homology 2-containing phosphatases 1 and 2, as did the tail of the inhibitory receptor KIR2DL1. Therefore, KIR2DL4 has inhibitory potential in addition to its activating function.
机译:KIR2DL4(CD158d)是在所有NK细胞和某些T细胞中表达的杀伤细胞Ig样受体家族的不寻常成员。尽管在其细胞质尾部存在基于免疫受体酪氨酸的抑制基序(ITIM),但KIR2DL4激活NK细胞的细胞毒性。该ITIM对KIR2DL4激活功能的作用及其是否可以提供抑制信号尚不清楚。设计了突变形式的KIR2DL4,其缺少ITIM中的酪氨酸或跨膜区域中的激活信号所需的精氨酸-酪氨酸基序。在重定向裂解测定中测试了突变的KIR2DL4分子的活性。 ITIM不是激活KIR2DL4裂解所必需的。 KIR2DL4的激活信号对另一个包含ITIM的受体的抑制作用敏感。 KIR2DL4的活化不足突变体抑制了活化受体CD16传递的信号。在使用GST融合蛋白的下拉实验中,KIR2DL4的酪氨酸磷酸化的胞质尾部与抑制受体KIR2DL1的尾部结合了含Src同源性2的磷酸酶1和2。因此,KIR2DL4除了具有激活功能外,还具有抑制作用。

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