Barcia R, García-Vargas S, Boscá L, Lazo P A
Unidad de Genetica Molecular (CSIC), Facultad de Farmacia, Madrid, Spain.
Cell Immunol. 1996 Apr 10;169(1):107-12. doi: 10.1006/cimm.1996.0097.
The CD53 antigen is a prototype member of the transmembrane-4 superfamily which includes several tumor antigens. In this report we have studied the changes in the cellular binding of phorbol esters after stimulation with monoclonal antibody (mAb) MRC OX-44 (anti-CD53) and epidermal growth factor (EGF) using a fluorochrome-phorbol ester binding assay. Incubation of a rat B cell lymphoma cell line with this mAb or EGF induces the appearance of high- and low-affinity phorbol ester binding sites and changes the total number of binding sites. Four binding sites with different characteristics have been detected. The binding data suggest that two structurally different receptors, CD53 antigen and EGF receptor, induce a similar change in the functional protein kinase C expressed in the cell which might be implicated in the responses elicited after cell stimulation.
CD53抗原是跨膜4超家族的原型成员,该超家族包括几种肿瘤抗原。在本报告中,我们使用荧光染料佛波酯结合试验,研究了用单克隆抗体(mAb)MRC OX-44(抗CD53)和表皮生长因子(EGF)刺激后佛波酯细胞结合的变化。用该单克隆抗体或EGF孵育大鼠B细胞淋巴瘤细胞系,可诱导高亲和力和低亲和力佛波酯结合位点的出现,并改变结合位点的总数。已检测到四个具有不同特征的结合位点。结合数据表明,两种结构不同的受体,即CD53抗原和EGF受体,可诱导细胞中表达的功能性蛋白激酶C发生类似变化,这可能与细胞刺激后引发的反应有关。