Borgya A, Woodman A, Sugiyama M, Donié F, Kopetzki E, Matsumura Y, Tarin D
Boehringer Mannheim GmbH, Nonnewald, D-82372 Penzberg, Germany.
Clin Mol Pathol. 1995 Oct;48(5):M241-50. doi: 10.1136/mp.48.5.m241.
Aims-Exon 7 of the human CD44 gene is overexpressed in many commonly occurring carcinomas. The aim of the study was to explore the diagnostic and therapeutic potential of this frequent abnormality.Methods-A new monoclonal antibody (mAb, M-23.6.1) and a polyclonal antibody (pAb,S-6127) to the corresponding antigen were raised by immunising mice and sheep, respectively, with a specially constructed fusion protein HIV2 (gp32)-CD44 exon 7.Results-Characterisation of mAb, M-23.6.1 by ELISA, western blotting, immunocytochemistry, and FACS analysis confirmed that it specifically recognises an epitope in the region between amino acids 19 and 33 of the peptide encoded by this exon. Western blotting experiments with two cell lines, RT112 and ZR75-1, known from RT-PCR data to be overtranscribing the exon, yielded a monospecific band of approximately 220 kDa, and immunocytochemistry showed discrete membrane staining on the same cell lines. Fluorescent antibody cell sorting (FACS) revealed binding to greater than 90% of the cells of each of these lines. Specificity of recognition of the antigen was shown by inhibition of the precise immunoreactivity typically seen in ELISA and Western blots, by pre-incubation with synthetic exon 7 peptide or fragments of it.Conclusions-The new antibodies will be useful tools for the further analysis of abnormal CD44 isoforms and their clinical implications.
目的——人类CD44基因的外显子7在许多常见癌症中过度表达。本研究的目的是探索这种常见异常的诊断和治疗潜力。
方法——分别用特殊构建的融合蛋白HIV2(gp32)-CD44外显子7免疫小鼠和绵羊,制备针对相应抗原的新型单克隆抗体(mAb,M-23.6.1)和多克隆抗体(pAb,S-6127)。
结果——通过ELISA、蛋白质印迹、免疫细胞化学和FACS分析对mAb M-23.6.1进行表征,证实它能特异性识别该外显子编码肽中氨基酸19至33之间区域的一个表位。对RT112和ZR75-1这两种细胞系进行蛋白质印迹实验,根据RT-PCR数据已知这两种细胞系过度转录该外显子,结果产生了一条约220 kDa的单特异性条带,免疫细胞化学显示这两种细胞系有离散的膜染色。荧光抗体细胞分选(FACS)显示与这些细胞系中每种细胞系的90%以上细胞结合。通过用合成外显子7肽或其片段预孵育,抑制ELISA和蛋白质印迹中通常所见的精确免疫反应性,证明了对抗原识别的特异性。
结论——这些新型抗体将成为进一步分析异常CD44异构体及其临床意义的有用工具。