Shintani A, Watanabe T, Kuroshima K, Ichimori Y, Kurokawa T, Igarashi K, Sasada R
Discovery Research Laboratory II, Takeda Chemical Industries Ltd., Osaka, Japan.
Biochem Biophys Res Commun. 1993 Aug 16;194(3):1500-7. doi: 10.1006/bbrc.1993.1994.
Hybridomas producing monoclonal antibodies (MoAbs) against human neurotrophin-3 (hNT-3) were established using recombinant hNT-3 produced in CHO cells and E. coli as immunogens. Of the five MoAbs obtained, MoAb 3w3 showed the highest antibody titer and also best neutralized NT-3 activity as measured by the survival of chick embryonic day-8 dorsal root ganglia neurons. A sandwich enzyme immunoassay (EIA) for NT-3 was established with solid phase MoAb 3W3 and the Fab' fragment of MoAb 3W3 conjugated to horseradish peroxidase. The detection limit was 2.7 pg/well of NT-3 and no cross-reactivity with nerve growth factor up to 100 ng/well was observed. Using this EIA system we have screened a variety of cell lines for NT-3 production. Among these tested, only human Burkitt's lymphoma Namalwa cells were found to be producing NT-3.
利用在CHO细胞和大肠杆菌中产生的重组人神经营养因子-3(hNT-3)作为免疫原,建立了产生抗人神经营养因子-3单克隆抗体(MoAb)的杂交瘤细胞系。在获得的5种单克隆抗体中,单克隆抗体3w3表现出最高的抗体滴度,并且在通过鸡胚胎第8天背根神经节神经元存活情况测定时,其对NT-3活性的中和效果最佳。利用固相单克隆抗体3W3和与辣根过氧化物酶偶联的单克隆抗体3W3的Fab'片段,建立了一种用于NT-3的夹心酶免疫测定(EIA)方法。NT-3的检测限为2.7 pg/孔,在高达100 ng/孔的情况下未观察到与神经生长因子的交叉反应。使用该EIA系统,我们筛选了多种细胞系以检测其NT-3的产生情况。在这些测试的细胞系中,仅发现人伯基特淋巴瘤Namalwa细胞产生NT-3。