Cao M Y, Davidson D, Yu J, Latour S, Veillette A
McGill Cancer Centre, McGill University, Montréal, Québec, Canada H3G 1Y6.
J Exp Med. 1999 Nov 15;190(10):1527-34. doi: 10.1084/jem.190.10.1527.
We have identified a novel Src homology 2 domain-containing leukocyte protein of 76 kD (SLP-76)-related molecule which we have termed Clnk (for cytokine-dependent hemopoietic cell linker). Unlike its relatives SLP-76 and B cell linker protein (Blnk), Clnk is not expressed uniformly within a given hemopoietic cell lineage. Even though it can be detected in several cell types, including T cells, natural killer cells, and mast cells, its expression seems to be strictly dependent on sustained exposure to cytokines such as interleukin (IL)-2 and IL-3. Strong support for the notion that Clnk is involved in immunoreceptor signaling was provided by the observation that it inducibly associated with at least one tyrosine-phosphorylated polypeptide (p92) in response to immunoreceptor stimulation. Moreover, transient expression of Clnk caused an increase in immunoreceptor-mediated signaling events in a T cell line. Taken together, these results show that Clnk is a novel member of the SLP-76 family selectively expressed in cytokine-stimulated hemopoietic cells. Furthermore, they suggest that Clnk may be involved in a cross-talk mechanism between cytokine receptor and immunoreceptor signaling.
我们鉴定出了一种新的与含Src同源2结构域的76kD白细胞蛋白(SLP-76)相关的分子,我们将其命名为Clnk(细胞因子依赖性造血细胞连接蛋白)。与它的亲属SLP-76和B细胞连接蛋白(Blnk)不同,Clnk在特定的造血细胞谱系中并非均匀表达。尽管它能在包括T细胞、自然杀伤细胞和肥大细胞在内的几种细胞类型中被检测到,但其表达似乎严格依赖于持续暴露于细胞因子,如白细胞介素(IL)-2和IL-3。有观察表明,Clnk在免疫受体刺激下可诱导与至少一种酪氨酸磷酸化多肽(p92)结合,这为Clnk参与免疫受体信号传导这一观点提供了有力支持。此外,Clnk的瞬时表达导致T细胞系中免疫受体介导的信号事件增加。综上所述,这些结果表明Clnk是SLP-76家族的一个新成员,在细胞因子刺激的造血细胞中选择性表达。此外,它们提示Clnk可能参与细胞因子受体和免疫受体信号传导之间的串扰机制。