Beattie J, Borromeo V, Bramani S, Secchi C, Baumbach W R, Mockridge J
Hannah Research Institute, Ayr KA6 5HL, UK.
J Mol Endocrinol. 1999 Dec;23(3):307-13. doi: 10.1677/jme.0.0230307.
We describe the properties of three monoclonal antibodies (MAbs) to ovine GH, two of which have previously been shown to enhance, in vivo, the biological activity of bovine and ovine growth hormone. We have examined the effects of these MAbs on GH activity in two appropriate GH-responsive cell culture systems, investigating both acute signalling effects (Janus-activated kinase (Jak)-2 tyrosine phosphorylation -5 min) and longer-term (MTT-formazan production -24 h) effects of hormone-antibody complexes. In the 3T3-F442A pre-adipocyte cell line (which has been demonstrated to be GH responsive), we show that complexation of recombinant bovine (rb) GH with either of the two enhancing anti-ovine GH MAbs (OA11 and OA15) and the non-enhancing MAb, OA14, attenuates the ability of GH to stimulate tyrosine phosphorylation of Jak-2 at a 5-min time point. Using the mouse myeloid cell line, FDC-P1, stably transfected with the full-length ovine GH receptor (oGHR), we demonstrate that rbGH causes a dose-dependent increase in MTT-formazan production by these cells. Further, we demonstrate that OA11 and OA14, but not OA15, cause a decrease in this stimulatory activity of rbGH over a hormone concentration range of 5-50 ng/ml at both 24 and 48 h. We conclude that the different in vitro activities of the two in vivo enhancing MAbs are most probably related to the time-courses over which these two assays are performed, and also to the relative affinities between antibody, hormone and receptor. In addition, the in vitro inhibitory activity of the enhancing MAb OA11 in both short- and long-term bioassay lends further support to an exclusively in vivo model for MAb-mediated enhancement of GH action.
我们描述了三种抗绵羊生长激素(GH)单克隆抗体(MAb)的特性,其中两种先前已证明在体内可增强牛和绵羊生长激素的生物活性。我们在两种合适的GH反应性细胞培养系统中研究了这些单克隆抗体对GH活性的影响,考察了激素-抗体复合物的急性信号转导效应(Janus激活激酶(Jak)-2酪氨酸磷酸化 - 5分钟)和长期效应(MTT-甲臜生成 - 24小时)。在3T3-F442A前脂肪细胞系(已证明对GH有反应)中,我们发现重组牛(rb)GH与两种增强型抗绵羊GH单克隆抗体(OA11和OA15)以及非增强型单克隆抗体OA14形成复合物后,在5分钟时间点会减弱GH刺激Jak-2酪氨酸磷酸化的能力。使用稳定转染了全长绵羊GH受体(oGHR)的小鼠髓样细胞系FDC-P1,我们证明rbGH可使这些细胞的MTT-甲臜生成呈剂量依赖性增加。此外,我们证明在24小时和48小时时,在5 - 50 ng/ml的激素浓度范围内,OA11和OA14(而非OA15)会使rbGH的这种刺激活性降低。我们得出结论,两种在体内具有增强作用的单克隆抗体的不同体外活性很可能与进行这两种检测的时间进程有关,也与抗体、激素和受体之间的相对亲和力有关。此外,增强型单克隆抗体OA11在短期和长期生物检测中的体外抑制活性进一步支持了单克隆抗体介导的GH作用增强仅存在于体内的模型。