Santos-Argumedo L, Teixeira C, Preece G, Kirkham P A, Parkhouse R M
Department of Immunology, National Institute for Medical Research, Mill Hill, London, U.K.
J Immunol. 1993 Sep 15;151(6):3119-30.
A rat mAb (NIM-R5) was prepared against a 42-kD B cell activation Ag (p42). The expression of p42 is increased upon activation. NIM-R5 induces an increase of intracellular Ca2+, due to influx from the exterior milieu via calcium channels. This stimulation does not prejudice further stimulation with anti-Ig, and thus p42 constitutes an activation signal independent of membrane Ig. The antibody induces increased expression of class II molecules on resting B lymphocytes and prepares the cells for "spreading" when interacted with immobilized anti-class II antibody. The antibody alone is weakly mitogenic and comitogenic with IL-4 on resting B cells. Of particular interest, NIM-R5 induces proliferation and rescue from apoptosis in B cells activated in vitro. In conclusion, NIM-R5 induces an Ig-independent activation and proliferation of resting and activated B cells. This antibody does not recognize other known B cell activation Ag such as CD23, CD40, or CD72. We therefore propose that the p42 Ag is a glycoprotein with an important role in the regulation of B lymphocyte activation and survival.
制备了一种针对42-kD B细胞活化抗原(p42)的大鼠单克隆抗体(NIM-R5)。p42的表达在活化时增加。NIM-R5可诱导细胞内Ca2+增加,这是由于通过钙通道从细胞外环境流入所致。这种刺激并不影响用抗Ig进行的进一步刺激,因此p42构成了一个独立于膜Ig的活化信号。该抗体可诱导静息B淋巴细胞上II类分子表达增加,并使细胞在与固定化抗II类抗体相互作用时做好“铺展”准备。单独的该抗体对静息B细胞有较弱的促有丝分裂作用,并与IL-4有协同促有丝分裂作用。特别值得注意的是,NIM-R5可诱导体外活化的B细胞增殖并使其免于凋亡。总之,NIM-R5可诱导静息和活化B细胞发生不依赖Ig的活化和增殖。该抗体不识别其他已知的B细胞活化抗原如CD23、CD40或CD72。因此我们提出p42抗原是一种糖蛋白,在B淋巴细胞活化和存活的调节中起重要作用。