Wang Yu-Cai, Zheng Lian-He, Ma Bao-An, Zhou Yong, Fan Qing-Yu
Department of Orthopaedic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi Province, China.
Hybridoma (Larchmt). 2010 Feb;29(1):13-6. doi: 10.1089/hyb.2009.0059.
Tenascin-C (TN-C), a key component of extracellular matrix (ECM), is strongly expressed in fetal and cancer tissues. Large-molecular-weight variants of TN-C, including different combinations of its alternative spliced FNIII repeats, are specifically expressed in tissues under certain pathological conditions. Here we report the production of monoclonal antibodies (MAbs) against FNIII domain D (FNIII D) of human TN-C. Complementary DNA encoding the FNIII D region was generated by RT-PCR from human osteosarcoma (OS) cell line, and the recombinant FNIII D-GST fusion protein was expressed and purified. Two hybridoma cell lines secreting monoclonal antibodies (MAbs) against FNIII D were obtained by routine murine hybridoma technique. The MAbs were identified by indirect enzyme-linked immunosorbent assay (ELISA), Western blot, and immunohistochemistry (IHC). Both of them were applicable in Western blot and IHC. With our MAbs, we found TN-C was positive in OS and most of it was among the tumor stroma. To conclude, these MAbs to human FNIII D domain of TN-C may be useful for exploring OS pathogenesis and potential clinical application.
腱生蛋白-C(TN-C)是细胞外基质(ECM)的关键成分,在胎儿组织和癌组织中强烈表达。TN-C的大分子变体,包括其可变剪接的纤连蛋白III(FNIII)重复序列的不同组合,在某些病理条件下的组织中特异性表达。在此,我们报告了针对人TN-C的FNIII结构域D(FNIII D)产生的单克隆抗体(MAb)。通过逆转录聚合酶链反应(RT-PCR)从人骨肉瘤(OS)细胞系中生成编码FNIII D区域的互补DNA,并表达和纯化重组FNIII D-谷胱甘肽S-转移酶(GST)融合蛋白。通过常规小鼠杂交瘤技术获得了两个分泌针对FNIII D的单克隆抗体的杂交瘤细胞系。通过间接酶联免疫吸附测定(ELISA)、蛋白质印迹法和免疫组织化学(IHC)对单克隆抗体进行鉴定。它们两者都适用于蛋白质印迹法和免疫组织化学。利用我们的单克隆抗体,我们发现TN-C在骨肉瘤中呈阳性,并且大部分位于肿瘤基质中。总之,这些针对TN-C人FNIII D结构域的单克隆抗体可能有助于探索骨肉瘤的发病机制和潜在的临床应用。