Sun Wan Ping, Wang Feng Ming, Xie Fang, Wang Guo Qing, Sun Jin, Yu Ge Hua, Qiu Yu Hua, Zhang Xue Guang
Institute of Biotechnology and Clinical Immunology, Research Laboratory of Jiangsu Province, Soochow University, Suzhou, China.
Cell Mol Immunol. 2007 Jun;4(3):209-14.
Syndecan-1 (CD138), a member of integral membrane heparin sulfate proteoglycans, is an essential matrix receptor for maintaining the normal morphological phenotypes. In this study, we generated a specific mouse anti-human syndecan-1 monoclonal antibody (mAb) 4B3 and identified it by competition assay with the available syndecan-1 mAb (BB4). Stained by 4B3, the expression of syndecan-1 was detected on tumor cell lines, such as 8226, U266, XG-1, XG-2, Daudi and Jurkat. The expression was also found on neuron stem cells. It was established that 4B3 mAb could inhibit XG-1 and XG-2 proliferation. The data not only determined that 4B3 mAb was a functional anti-human syndecan-1 mAb, but also indicated that syndecan-1 might be a valuable surface antigen and play an important role in regulation of tumor pathology and differentiation of neural stem cells. This novel antibody 4B3 may be value of study of tumor proliferation/survival mechanism and contributes to diagnosis and treatment of diverse diseases.
Syndecan-1(CD138)是整合膜硫酸乙酰肝素蛋白聚糖家族成员之一,是维持正常形态表型所必需的基质受体。在本研究中,我们制备了一种特异性小鼠抗人syndecan-1单克隆抗体(mAb)4B3,并通过与现有的syndecan-1 mAb(BB4)竞争试验对其进行了鉴定。用4B3染色后,在8226、U266、XG-1、XG-2、Daudi和Jurkat等肿瘤细胞系上检测到syndecan-1的表达。在神经干细胞上也发现了这种表达。已证实4B3 mAb可抑制XG-1和XG-2的增殖。这些数据不仅确定4B3 mAb是一种功能性抗人syndecan-1 mAb,还表明syndecan-1可能是一种有价值的表面抗原,在肿瘤病理调节和神经干细胞分化中发挥重要作用。这种新型抗体4B3可能对肿瘤增殖/存活机制的研究有价值,并有助于多种疾病的诊断和治疗。