The development and characterization of an eluted stain assay (ESTA) for the insulin-like growth factors.

Growth regulation Pub Date : 1993-12-01
D C Claffey, M E Yateman, P A Lane, P A Ealey, J A Wass, N J Marshall, J M Holly
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Abstract

An Eluted Stain Assay System (ESTA) has been adapted for the bioassay of the insulin-like growth factors, IGF-I and IGF-II. This ESTA is based on the Fischer Rat Thyroid cell line FRTL-5 which was grown as uniform, adherent microcultures on 96-well microtitre plates. The cells were stimulated with the growth factors for 48 h in hormone and serum free conditions. Responses were determined by the addition of the tetrazolium salt MTT which was reduced to a purple formazan product in a dose related manner. This was directly eluted from the cells and measured with a microtitre plate reader. The signal generated was solely dependent on metabolic activation of the cells, since no increase in cell numbers was detected during the bioassay. The advantages of using this method are its sensitivity, precision, specificity, rapidity and high sample throughout. This bioassay, which is based on a colorimetric method, is technically convenient compared with other systems including the earlier cytochemical bioassays and the radioisotopic methods. We have demonstrated that this MTT ESTA provides a useful method for the study of complex interactions between IGF-I and IGF-II and their related binding proteins and that IGF bioactivity in serum may also be investigated using this ESTA bioassay.

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胰岛素样生长因子的洗脱染色试验(ESTA)的发展和特性。
洗脱染色分析系统(ESTA)已适应于胰岛素样生长因子,IGF-I和IGF-II的生物测定。ESTA是基于Fischer大鼠甲状腺细胞系FRTL-5,该细胞系在96孔微滴板上均匀贴壁培养。在无激素和无血清条件下,用生长因子刺激细胞48 h。通过添加四氮唑盐MTT来确定反应,四氮唑盐MTT以剂量相关的方式还原为紫色的福马赞产物。直接从细胞中洗脱,用微滴板读取器测量。产生的信号完全依赖于细胞的代谢激活,因为在生物测定过程中没有检测到细胞数量的增加。该方法具有灵敏度高、精密度高、特异度高、快速等优点。这种基于比色法的生物测定在技术上与其他系统(包括早期的细胞化学生物测定和放射性同位素方法)相比是方便的。我们已经证明这种MTT ESTA为研究IGF- i和IGF- ii及其相关结合蛋白之间的复杂相互作用提供了一种有用的方法,并且使用ESTA生物测定法也可以研究血清中IGF的生物活性。
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