Taylor J A, Karas J L, Ram M K, Green O M, Seidel-Dugan C
ARIAD Pharmaceuticals, Cambridge, Massachusetts 02139, USA.
Mol Cell Biol. 1995 Aug;15(8):4149-57. doi: 10.1128/MCB.15.8.4149.
Antigen-mediated aggregation of the high-affinity receptor for immunoglobulin E, Fc epsilon RI, results in the activation of multiple signaling pathways, leading to the release of mediators of the allergic response. One of the earliest responses to receptor stimulation is the tyrosine phosphorylation of the beta and gamma subunits of Fc epsilon RI and the association of the tyrosine kinase Syk with the phosphorylated receptor. This association is mediated by the SH2 domains of Syk and is believed to be critical for activating signaling pathways resulting in mediator release. To examine the importance of the interaction of Syk with Fc epsilon RI in signaling events following receptor activation, we introduced a protein containing the SH2 domains of Syk into streptolysin O-permeabilized RBL-2H3 cells. The Syk SH2 domains completely inhibited degranulation and leukotriene production following receptor aggregation, and they blocked the increase in protein tyrosine phosphorylation observed after receptor activation. Inhibition was specific for Fc epsilon RI-mediated signaling, since degranulation of cells activated by alternative stimuli was not blocked by the Syk SH2 domains. A protein containing a point mutation in the carboxy-terminal SH2 domain which abolishes phosphotyrosine binding was not inhibitory. In addition, inhibition of degranulation was reversed by pretreatment of the SH2 domains with a tyrosine phosphorylated peptide corresponding to the tyrosine-based activation motif found in the gamma subunit of Fc epsilon RI, the nonphosphorylated peptide had no effect. The association of Syk with the tyrosine-phosphorylated gamma subunit of the activated receptor was blocked by the Syk SH2 domains, and deregulation in cells activated by clustering of Syk directly without Fc epsilon RI aggregation was not affected by the Syk SH2 domains. These results demonstrate that the association of Syk with the activated Fc epsilon RI is critical for both early and late events following receptor activation and confirm the key role Syk plays in signaling through the high-affinity IgE receptor.
抗原介导的免疫球蛋白E高亲和力受体FcεRI聚集,会激活多条信号通路,导致过敏反应介质的释放。对受体刺激的最早反应之一是FcεRI的β和γ亚基发生酪氨酸磷酸化,以及酪氨酸激酶Syk与磷酸化受体结合。这种结合由Syk的SH2结构域介导,被认为对激活导致介质释放的信号通路至关重要。为了研究Syk与FcεRI的相互作用在受体激活后信号事件中的重要性,我们将一种含有Syk的SH2结构域的蛋白导入经链球菌溶血素O通透处理的RBL-2H3细胞中。Syk的SH2结构域在受体聚集后完全抑制了脱颗粒和白三烯的产生,并且阻断了受体激活后观察到的蛋白酪氨酸磷酸化增加。这种抑制对FcεRI介导的信号传导具有特异性,因为由其他刺激激活的细胞脱颗粒不受Syk的SH2结构域的阻断。一种在羧基末端SH2结构域含有点突变从而消除磷酸酪氨酸结合的蛋白没有抑制作用。此外,用对应于FcεRIγ亚基中基于酪氨酸的激活基序的酪氨酸磷酸化肽预处理SH2结构域可逆转脱颗粒的抑制,非磷酸化肽则没有作用。Syk的SH2结构域阻断了Syk与激活受体的酪氨酸磷酸化γ亚基的结合,并且直接通过Syk聚集而不通过FcεRI聚集激活的细胞中的信号失调不受Syk的SH2结构域的影响。这些结果表明,Syk与激活的FcεRI的结合对于受体激活后的早期和晚期事件都至关重要,并证实了Syk在通过高亲和力IgE受体进行信号传导中所起的关键作用。