Clnk, a novel SLP-76-related adaptor molecule expressed in cytokine-stimulated hemopoietic cells

被引:53
作者
Cao, MY
Davidson, D
Yu, J
Latour, S
Veillette, A
机构
[1] McGill Univ, Ctr Canc, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[3] McGill Univ, Dept Oncol, Montreal, PQ H3G 1Y6, Canada
[4] McGill Univ, Dept Med, Montreal, PQ H3G 1Y6, Canada
关键词
adaptor; SLP-76; Blnk; signaling; lymphocytes;
D O I
10.1084/jem.190.10.1527
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have identified a novel Src homology 2 domain-containing leukocyte protein of 76 kD (SLP-76)-related molecule which wt 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 chat 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.
引用
收藏
页码:1527 / 1534
页数:8
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