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牛共刺激分子。I. 无血清伊斯科夫培养基中的产生动力学、部分纯化及定量分析。

Bovine costimulator. I. Production kinetics, partial purification, and quantification in serum-free Iscove's medium.

作者信息

Baker P E, Knoblock K F

出版信息

Vet Immunol Immunopathol. 1982 Jul;3(4):365-79. doi: 10.1016/0165-2427(82)90020-4.

Abstract

Bovine peripheral blood leukocytes were examined for blast transformation in response to T-cell lectins in serum-containing RPMI 1640 medium and serum-free Iscove's medium. Phytohemagglutinin-induced blastogenesis was significantly greater in Iscove's medium than in RPMI containing ten percent fetal calf serum. Concanavalin A-induced blast transformation was equivalent in both media. However, the kinetics of lectin response and the quantity of lectin required for optimum blastogenesis was considerably different in the two culture media. Concanavalin A-induced blast transformation of bovine thymocytes in Iscove's medium revealed that a concentration of 10(6) cells/ml, inconsequential blastogenesis ensued; but at 10(7) cells/ml blast transformation was significant and dose-dependent. Therefore, conditioned media from concanavalin A-stimulated bovine peripheral blood leukocytes, prepared in serum-free Iscove's medium, were assayed for costimulator activity using bovine thymocytes at 10(6) cells/ml in Iscove's medium as indicator cells. Both optimum lectin requirements and cell concentrations for production of costimulator activity were found. Conditioned medium, operated with the total exclusion of serum and with optimal costimulator activity, was fractionated via gel exclusion chromatography. A quantitative assay was described, and results indicated that bovine costimulator had an approximate molecular weight of 20,000 daltons.

摘要

在含血清的RPMI 1640培养基和无血清的伊斯科夫培养基中,检测牛外周血白细胞对T细胞凝集素的增殖转化反应。在伊斯科夫培养基中,植物血凝素诱导的增殖反应明显强于含10%胎牛血清的RPMI培养基。刀豆球蛋白A诱导的增殖转化在两种培养基中相当。然而,两种培养基中凝集素反应的动力学以及最佳增殖所需的凝集素量有很大差异。在伊斯科夫培养基中,刀豆球蛋白A诱导的牛胸腺细胞增殖转化显示,细胞浓度为10⁶个细胞/ml时,增殖反应不明显;但细胞浓度为10⁷个细胞/ml时,增殖转化显著且呈剂量依赖性。因此,以伊斯科夫培养基中10⁶个细胞/ml的牛胸腺细胞为指示细胞,检测在无血清伊斯科夫培养基中制备的刀豆球蛋白A刺激的牛外周血白细胞条件培养基的共刺激活性。确定了产生共刺激活性所需的最佳凝集素用量和细胞浓度。对完全不含血清且具有最佳共刺激活性的条件培养基进行凝胶排阻色谱分离。描述了一种定量测定方法,结果表明牛共刺激因子的分子量约为20,000道尔顿。

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