Ikeda M, Wada M, Fujita Y, Takahashi S, Maekawa K, Honjo M
Life Science Laboratories, Mitsui Chemicals Inc., Mobara, Chiba, Japan.
Growth Horm IGF Res. 2000 Oct;10(5):248-55. doi: 10.1054/ghir.2000.0163.
Previously we introduced the full-length hGH receptor (hGHR) into the mouse pro-B cell line, Ba/F3, and obtained stable transfectant (Ba/F3-hGHR), which could grow in response to 20K- and 22K-hGH in a dose-dependent manner(1). In the present study, we established a new bioassay system based on the proliferation of the Ba/F3-hGHR in combination with the eluted stain assay (ESTA). The Ba/F3-hGHR assay is completed in 18 h and requires only 10(-6)-fold amount of GH sample (1.8 ng) as compared with the rat weight gain assay. The validation study shows that the Ba/F3-hGHR assay is specific for hGH, precise (RSD = 1.1-19.7%) and ultrasensitive (lower limit of working range = 18.7 pg/mL). Four modified forms of recombinant 20K-hGH (oxidized, deamidated, des-Phe(1)and cleaved form) all of which are newly identified were measured by the Ba/F3-hGHR assay and the rat weight gain assay with our in-house recombinant 20K-hGH as standard. The oxidized and deamidated 20K-hGH were fully active, however the des-Phe(1)and cleaved 20K-hGH had significantly reduced activities in both assays. These findings suggest that the Ba/F3-hGHR assay is useful as an alternative to the rat weight gain assay.
此前,我们将全长人生长激素受体(hGHR)导入小鼠前B细胞系Ba/F3中,获得了稳定转染子(Ba/F3-hGHR),其能够以剂量依赖的方式对20K-和22K-人生长激素产生反应(1)。在本研究中,我们基于Ba/F3-hGHR的增殖并结合洗脱染色测定法(ESTA)建立了一种新的生物测定系统。Ba/F3-hGHR测定在18小时内完成,与大鼠体重增加测定相比,所需的生长激素样品量仅为其10^(-6)倍(1.8 ng)。验证研究表明,Ba/F3-hGHR测定对人生长激素具有特异性、精密度高(相对标准偏差=1.1-19.7%)且超灵敏(工作范围下限=18.7 pg/mL)。以我们内部重组的20K-人生长激素为标准品,通过Ba/F3-hGHR测定和大鼠体重增加测定对新鉴定出的四种重组20K-人生长激素的修饰形式(氧化型、脱酰胺型、去苯丙氨酸(1)型和裂解型)进行了测定。氧化型和脱酰胺型20K-人生长激素具有完全活性,然而去苯丙氨酸(1)型和裂解型20K-人生长激素在两种测定中的活性均显著降低。这些发现表明,Ba/F3-hGHR测定可作为大鼠体重增加测定的替代方法。