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首页> 外文期刊>Developmental and Comparative Immunology: Ontogeny, Phylogeny, Aging: The Official Journal of the International Society of Developmental and Comparative Immunology >Cell surface expression of channel catfish leukocyte immune-type receptors (IpLITRs) and recruitment of both Src homology 2 domain-containing protein tyrosine phosphatase (SHP)-1 and SHP-2
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Cell surface expression of channel catfish leukocyte immune-type receptors (IpLITRs) and recruitment of both Src homology 2 domain-containing protein tyrosine phosphatase (SHP)-1 and SHP-2

机译:channel鱼白细胞免疫型受体(IpLITRs)的细胞表面表达以及包含Src同源2域的蛋白酪氨酸磷酸酶(SHP)-1和SHP-2的募集

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摘要

Channel catfish leukocyte immune-type receptors (IpLITRs) are immunoglobulin superfamily (IgSF) members believed to play a role in the control and coordination of cellular immune responses in teleost. Putative stimulatory and inhibitory IpLITRs are co-expressed by different types of catfish immune cells (e.g. NK cells, T cells, B cells, and macrophages) but their signaling potential has not been determined. Following cationic polymer-mediated transfections into human cell lines we examined the surface expression, tyrosine phosphorylation, and phosphatase recruitment potential of two types of putative inhibitory IpLITRs using 'chimeric' expression constructs and an epitope-tagged 'native' IpLITR. We also cloned and expressed the teleost Src homology 2 domain-containing protein tyrosine phosphatases (SHP)-1 and SHP-2 and examined their expression in adult tissues and developing zebrafish embryos. Coimmunoprecipitation experiments support the inhibitory signaling potential of distinct IpLITR-types that bound both SHP-1 and SHP-2 following the phosphorylation of tyrosine residues within their cytoplasmic tail (CYT) regions. Phosphatase recruitment by IpLITRs represents an important first step in understanding their influence on immune cell effector functions and suggests that certain inhibitory signaling pathways are conserved among vertebrates.
机译:鱼白细胞免疫型受体(IpLITRs)是免疫球蛋白超家族(IgSF)成员,据信在硬骨鱼的细胞免疫反应的控制和协调中发挥作用。推定的刺激性IpLITRs和抑制性IpLITRs由不同类型的of鱼免疫细胞(例如NK细胞,T细胞,B细胞和巨噬细胞)共表达,但尚未确定它们的信号传导潜能。在阳离子聚合物介导的人类细胞系转染后,我们使用“嵌合”表达构建体和带表位标签的“天然” IpLITR检查了两种类型的抑制性IpLITR的表面表达,酪氨酸磷酸化和磷酸酶募集潜力。我们还克隆并表达了硬骨鱼Src同源2域包含蛋白酪氨酸磷酸酶(SHP)-1和SHP-2,并检查了它们在成年组织和发育中的斑马鱼胚胎中的表达。免疫共沉淀实验支持在胞质尾部(CYT)区域内酪氨酸残基磷酸化后,结合SHP-1和SHP-2的不同IpLITR类型的抑制信号潜能。 IpLITRs募集磷酸酶代表了了解其对免疫细胞效应子功能的影响的重要的第一步,并表明某些抑制性信号通路在脊椎动物之间是保守的。

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