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4-1BB T细胞抗原与成熟B细胞和巨噬细胞结合,并共刺激抗μ致敏的脾B细胞。

4-1BB T-cell antigen binds to mature B cells and macrophages, and costimulates anti-mu-primed splenic B cells.

作者信息

Pollok K E, Kim Y J, Hurtado J, Zhou Z, Kim K K, Kwon B S

机构信息

Indiana University School of Medicine, Indianapolis 46202.

出版信息

Eur J Immunol. 1994 Feb;24(2):367-74. doi: 10.1002/eji.1830240215.

Abstract

4-1BB is expressed on activated murine T cells and may function as an accessory signaling molecule during T-cell activation. To identify putative 4-1BB ligands, a fusion protein consisting of the extracellular domain of 4-1BB fused to human placental alkaline phosphatase (4-1BB-AP) was constructed. Alkaline phosphatase activity could then be used as an indicator of the relative amount of bound 4-1BB. These studies indicated that 4-1BB-AP specifically bound to the surface of various mature B and macrophage cell lines. 4-1BB-AP bound at low levels to T cell lines (non-activated and anti-CD3-activated), pre-B-cell lines, and an immature macrophage cell line. 4-1BB-AP did not bind to a glial tumor cell line, HeLa cells, or COS cells. In addition, 4-1BB-AP bound at higher levels to F(ab')2 anti-mu-activated primary B cells compared to anti-CD3-activated primary T cells. Scatchard analysis indicated that the A20 B cell lymphoma expressed 3680 binding sites per cell with a Kd of 1.86 nM. Affinity cross-linking studies demonstrated that a major cell surface species of 120 kDa bound to 4-1BB-AP; 4-1BB-AP also bound to a minor species of approximately 60 kDa. The addition of paraformaldehyde-fixed SF21 cells expressing recombinant 4-1BB synergized with F(ab')2 anti-mu in inducing splenic B cell proliferation suggesting that 4-1BB may function as a regulator of B cell growth.

摘要

4-1BB在活化的小鼠T细胞上表达,在T细胞活化过程中可能作为辅助信号分子发挥作用。为了鉴定假定的4-1BB配体,构建了一种由4-1BB的细胞外结构域与人胎盘碱性磷酸酶融合而成的融合蛋白(4-1BB-AP)。然后,碱性磷酸酶活性可作为结合的4-1BB相对量的指标。这些研究表明,4-1BB-AP特异性结合各种成熟B细胞和巨噬细胞系的表面。4-1BB-AP与T细胞系(未活化和抗CD3活化的)、前B细胞系和未成熟巨噬细胞系的结合水平较低。4-1BB-AP不与胶质细胞瘤细胞系、HeLa细胞或COS细胞结合。此外,与抗CD3活化的原代T细胞相比,4-1BB-AP与F(ab')2抗μ活化的原代B细胞的结合水平更高。Scatchard分析表明,A20 B细胞淋巴瘤每个细胞表达3680个结合位点,解离常数为1.86 nM。亲和交联研究表明,一种主要的120 kDa细胞表面物质与4-1BB-AP结合;4-1BB-AP也与一种约60 kDa的次要物质结合。添加表达重组4-1BB的多聚甲醛固定的SF21细胞与F(ab')2抗μ协同作用,诱导脾B细胞增殖,提示4-1BB可能作为B细胞生长的调节因子发挥作用。

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