Pochet R, Delespesse G, Gausset P W, Collet H
Clin Exp Immunol. 1979 Dec;38(3):578-84.
A technique is described allowing the quantification and the characterization of specific beta-adrenergic receptors in intact living human lymphocytes. 125I-Iodohydroxybenzylpindolol, a potent beta-adrenergic antagonist was used to label specific binding sites on unfractionated lymphoid cells and on purified subpopulations of T (F1 and F2) and B cells. F1 and F2 were obtained by filtration through nylon wool column as previously described (Delespesse et al., 1976), they differ in their response to mitogens, and in their interactions with adherent cells and B cells. 125I-HYP binding to unfractionated lymphocytes was a saturable, stereospecific and rapid process with a dissociation constant of 2.5 10(-10) M and a binding capacity of 400--600 sites/cell. Bindings on unfractionated lymphocytes, purified B cells and T cells of the F2 fraction were similar. No detectable binding was noted on T cells from the F1 fraction. Enriched T cells obtained by a rosetting technique displayed 200 receptors/cell.
本文描述了一种技术,可对完整活的人淋巴细胞中的特定β-肾上腺素能受体进行定量和表征。使用强效β-肾上腺素能拮抗剂125I-碘羟基苄基吲哚洛尔标记未分级的淋巴细胞以及T细胞(F1和F2)和B细胞的纯化亚群上的特异性结合位点。F1和F2是通过如前所述(Delespesse等人,1976年)通过尼龙毛柱过滤获得的,它们在对有丝分裂原的反应以及与黏附细胞和B细胞的相互作用方面存在差异。125I-HYP与未分级淋巴细胞的结合是一个可饱和、立体特异性且快速的过程,解离常数为2.5×10(-10)M,结合容量为400-600个位点/细胞。未分级淋巴细胞、纯化的B细胞和F2亚群的T细胞上的结合情况相似。在F1亚群的T细胞上未观察到可检测到的结合。通过玫瑰花结技术获得的富集T细胞显示有200个受体/细胞。