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SHP-1通过与c-Kit近膜结构域中的酪氨酸569相互作用来结合并负向调节c-Kit受体。

SHP-1 binds and negatively modulates the c-Kit receptor by interaction with tyrosine 569 in the c-Kit juxtamembrane domain.

作者信息

Kozlowski M, Larose L, Lee F, Le D M, Rottapel R, Siminovitch K A

机构信息

Health Canada Life Sciences and the University of Ottawa, Canada.

出版信息

Mol Cell Biol. 1998 Apr;18(4):2089-99. doi: 10.1128/MCB.18.4.2089.

Abstract

The SH2 domain-containing SHP-1 tyrosine phosphatase has been shown to negatively regulate a broad spectrum of growth factor- and cytokine-driven mitogenic signaling pathways. Included among these is the cascade of intracellular events evoked by stem cell factor binding to c-Kit, a tyrosine kinase receptor which associates with and is dephosphorylated by SHP-1. Using a series of glutathione S-transferase (GST) fusion proteins containing either tyrosine-phosphorylated segments of the c-Kit cytosolic region or the SH2 domains of SHP-1, we have shown that SHP-1 interacts with c-Kit by binding selectively to the phosphorylated c-Kit juxtamembrane region and that the association of c-Kit with the larger of the two SHP-1 isoforms may be mediated through either the N-terminal or C-terminal SHP-1 SH2 domain. The results of binding assays with mutagenized GST-Kit juxtamembrane fusion proteins and competitive inhibition assays with phosphopeptides encompassing each c-Kit juxtamembrane region identified the tyrosine residue at position 569 as the major site for binding of SHP-1 to c-Kit and suggested that tyrosine 567 contributes to, but is not required for, this interaction. By analysis of Ba/F3 cells retrovirally transduced to express c-Kit receptors, phenylalanine substitution of c-Kit tyrosine residue 569 was shown to be associated with disruption of c-Kit-SHP-1 binding and induction of hyperproliferative responses to stem cell factor. Although phenylalanine substitution of c-Kit tyrosine residue 567 in the Ba/F3-c-Kit cells did not alter SHP-1 binding to c-Kit, the capacity of a second c-Kit-binding tyrosine phosphatase, SHP-2, to associate with c-Kit was markedly reduced, and the cells again showed hyperproliferative responses to stem cell factor. These data therefore identify SHP-1 binding to tyrosine 569 on c-Kit as an interaction pivotal to SHP-1 inhibitory effects on c-Kit signaling, but they indicate as well that cytosolic protein tyrosine phosphatases other than SHP-1 may also negatively regulate the coupling of c-Kit engagement to proliferation.

摘要

含SH2结构域的SHP-1酪氨酸磷酸酶已被证明对多种生长因子和细胞因子驱动的有丝分裂信号通路具有负调控作用。其中包括干细胞因子与c-Kit结合所引发的一系列细胞内事件,c-Kit是一种酪氨酸激酶受体,与SHP-1结合并被其去磷酸化。通过使用一系列含有c-Kit胞质区域酪氨酸磷酸化片段或SHP-1的SH2结构域的谷胱甘肽S-转移酶(GST)融合蛋白,我们发现SHP-1通过选择性结合磷酸化的c-Kit近膜区域与c-Kit相互作用,并且c-Kit与两种SHP-1同工型中较大的一种的结合可能通过N端或C端的SHP-1 SH2结构域介导。用诱变的GST-Kit近膜融合蛋白进行结合测定以及用包含每个c-Kit近膜区域的磷酸肽进行竞争性抑制测定的结果确定,第569位酪氨酸残基是SHP-1与c-Kit结合的主要位点,并表明第567位酪氨酸对这种相互作用有贡献,但不是必需的。通过分析逆转录病毒转导以表达c-Kit受体的Ba/F3细胞,发现c-Kit酪氨酸残基569被苯丙氨酸取代与c-Kit-SHP-1结合的破坏以及对干细胞因子的过度增殖反应的诱导有关。尽管在Ba/F3-c-Kit细胞中c-Kit酪氨酸残基567被苯丙氨酸取代并未改变SHP-1与c-Kit的结合,但第二种与c-Kit结合的酪氨酸磷酸酶SHP-2与c-Kit结合的能力明显降低,并且这些细胞再次显示出对干细胞因子的过度增殖反应。因此,这些数据确定SHP-1与c-Kit上的酪氨酸569结合是SHP-1对c-Kit信号传导抑制作用的关键相互作用,但它们也表明,除SHP-1外的胞质蛋白酪氨酸磷酸酶也可能对c-Kit参与与增殖的偶联产生负调控作用。

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