Randall L A, Wadhwa M, Thorpe R, Mire-Sluis A R
Division of Immunobiology, National Institute for Biological Standards and Control, Potters Bar, Herts, UK.
J Immunol Methods. 1993 Aug 26;164(1):61-7. doi: 10.1016/0022-1759(93)90276-d.
We have developed a simple, sensitive bioassay for transforming growth factors beta 1 and beta 2 (TGF-beta 1 and TGF-beta 2) based on the ability of these cytokines to inhibit the interleukin-5 induced proliferation of the erythroleukaemia cell line, TF-1. This assay is rapid, reproducible and sensitive to less than 500 fg/ml of TGF-beta 1, and 5-10 pg/ml TGF-beta 2. The assay is 100-1000-fold less sensitive to other inhibitory molecules such as interferon-beta, interferon-gamma and TNF-alpha. The assay can be made specific for TGF-beta 1 or TGF-beta 2 by including specific neutralising antibodies for TGF-beta 1 or TGF-beta 2. The assay can recognise all the readily available recombinant molecular species of these molecules as well as the natural proteins produced from human and bovine platelets and detects TGF-beta in serum samples.
我们基于转化生长因子β1和β2(TGF-β1和TGF-β2)抑制白细胞介素-5诱导的红白血病细胞系TF-1增殖的能力,开发了一种简单、灵敏的生物测定法。该测定法快速、可重复,对低于500 fg/ml的TGF-β1和5-10 pg/ml的TGF-β2敏感。该测定法对其他抑制分子如干扰素-β、干扰素-γ和肿瘤坏死因子-α的敏感性低100-1000倍。通过加入TGF-β1或TGF-β2的特异性中和抗体,该测定法可针对TGF-β1或TGF-β2进行特异性检测。该测定法能够识别这些分子所有现有的重组分子形式以及人源和牛源血小板产生的天然蛋白,并能检测血清样本中的TGF-β。