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Substance P Increases Cell-Surface Expression of CD74 (Receptor for Macrophage Migration Inhibitory Factor): In Vivo Biotinylation of Urothelial Cell-Surface Proteins

机译:P物质增加CD74(巨噬细胞迁移抑制因子的受体)的细胞表面表达:尿道上皮细胞表面蛋白的体内生物素化

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摘要

Macrophage migration inhibitory factor (MIF), an inflammatory cytokine, and its receptor CD74 are upregulated by bladder inflammation. MIF-mediated signal transduction involves binding to cell-surface CD74, this study documents, in vivo, MIF-CD74 interactions at the urothelial cell surface.N-hydroxysulfosuccinimide biotin ester-labeled surface urothelial proteins in rats treated either with saline or substance P (SP, 40 μg/kg). The bladder was examined by histology and confocal microscopy. Biotinylated proteins were purified by avidin agarose, immunoprecipitated with anti-MIF or anti-CD74 antibodies, and detected with strepavidin-HRP. Only superficial urothelial cells were biotinylated. These cells contained a biotinylated MIF/CD74 cell-surface complex that was increased in SP-treated animals. SP treatment increased MIF and CD74 mRNA in urothelial cells. Our data indicate that intraluminal MIF, released from urothelial cells as a consequence of SP treatment, interacts with urothelial cell-surface CD74. These results document that our previously described MIF-CD74 interaction occurs at the urothelial cell surface.
机译:巨噬细胞迁移抑制因子(MIF),一种炎症细胞因子及其受体CD74被膀胱炎症上调。 MIF介导的信号转导涉及与细胞表面CD74的结合,该研究在体内记录了尿路上皮细胞表面MIF-CD74的相互作用。 SP,40μg/ kg)。通过组织学和共聚焦显微镜检查膀胱。用抗生物素蛋白琼脂糖纯化生物素化的蛋白质,用抗MIF或抗CD74抗体免疫沉淀,并用链霉亲和素HRP检测。仅表面尿路上皮细胞被生物素化。这些细胞含有生物素化的MIF / CD74细胞表面复合物,在SP处理的动物中增加。 SP处理可增加尿路上皮细胞中的MIF和CD74 mRNA。我们的数据表明,由于SP治疗而从尿路上皮细胞释放的管腔内MIF与尿路上皮细胞表面CD74相互作用。这些结果证明我们先前描述的MIF-CD74相互作用发生在尿路上皮细胞表面。

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