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Molecular interactions of complement receptors on B lymphocytes: a CR1/CR2 complex distinct from the CR2/CD19 complex

机译:B淋巴细胞上补体受体的分子相互作用:不同于CR2 / CD19复合物的CR1 / CR2复合物

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摘要

The complement system augments the humoral immune response to low concentrations of antigen. This effect may be partly mediated by complement receptors on the surface of B lymphocytes that bind immunogenic complexes bearing fragments of C3 and C4. We have shown by immunoprecipitation analysis that the two complement receptors expressed by B lymphocytes, complement receptor 1 (CR1) and CR2, form a detergent-sensitive complex on the surface of tonsillar B lymphocytes and on K562 erythroleukemia cells that were co-transfected with cDNAs encoding CR1 and CR2. The CR1/CR2 complex is distinct from the CR2/CD19 complex and may assist B cell activation by efficiently capturing C3b- containing immunogens and maintaining such immunogens on the B cell after CR1 and factor I-mediated cleavage to iC3b and C3dg. The complement activating immunogen may then trigger signal transduction by the CR1/CR2 complex, the CR2/CD19 complex, or membrane immunoglobulin.
机译:补体系统增强了对低浓度抗原的体液免疫反应。这种作用可能部分由B淋巴细胞表面的补体受体介导,这些受体结合带有C3和C4片段的免疫原性复合物。我们已经通过免疫沉淀分析表明,B淋巴细胞表达的两个补体受体,补体受体1(CR1)和CR2,在扁桃体B淋巴细胞的表面以及与cDNA共转染的K562红白血病细胞上形成了去污剂敏感的复合物。编码CR1和CR2。 CR1 / CR2复合物不同于CR2 / CD19复合物,并可以通过有效捕获含C3b的免疫原并在CR1和因子I介导的iC3b和C3dg裂解后在B细胞上维持此类免疫原来辅助B细胞活化。然后补体激活免疫原可以触发CR1 / CR2复合物,CR2 / CD19复合物或膜免疫球蛋白的信号转导。

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