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Src-like adaptor protein (SLAP) is upregulated in antigen-stimulated mast cells and acts as a negative regulator.

机译:Src样衔接蛋白(SLAP)在抗原刺激的肥大细胞中上调,并起负调节剂的作用。

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Our studies in the RBL-2H3 mast cell line suggest that responses to antigen (Ag) are negatively modulated through upregulation of Src-like adaptor protein (SLAP). Ag stimulation of RBL-2H3 cells leads to increased levels of SLAP (but not SLAP2) transcripts and protein over a period of several hours. The effects of pharmacologic inhibitors indicate that the upregulation of SLAP is dependent on multiple signaling pathways. Knockdown of SLAP with anti-SLAP siRNA is associated with enhanced phosphorylation of Syk, the linker for activation of T cells (LAT), phospholipase C gamma, MAP kinases, and various transcription factors. Production of IL-3 and MCP-1, but not degranulation, is also enhanced. The upregulation of SLAP may thus serve to limit the duration of cytokine production in Ag-stimulated cells.
机译:我们在RBL-2H3肥大细胞系中的研究表明,通过上调Src样衔接蛋白(SLAP)对抗原(Ag)的反应负调节。 Ag刺激RBL-2H3细胞导致在数小时内SLAP(而非SLAP2)转录本和蛋白质水平增加。药理抑制剂的作用表明SLAP的上调取决于多种信号通路。用抗SLAP siRNA抑制SLAP与Syk磷酸化,T细胞活化的连接子(LAT),磷脂酶Cγ,MAP激酶和各种转录因子有关。 IL-3和MCP-1的产生,但不脱粒也得到增强。因此,SLAP的上调可用于限制Ag刺激细胞中细胞因子产生的持续时间。

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