Physicochemical characterization of the cytosol glucocorticoid receptors in various lymphoid tissues.

P Arányi, A Náray
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Abstract

Cytosol glucocorticoid receptors of five different lymphoid tissues of chicken and rats were characterized and compared by physicochemical parameters. Binding specificity of receptors was found to be similar, except that cytosol receptors of chick tissues appeared slightly more specific for dexamethasone than those from rats. Association rate constants of the dexamethasone-receptor complex were higher by about one order of magnitude in the case of chicken thymus and bursa than in other cytosols. Dissociation of dexamethasone-receptor complex occurred in one step in rat tissues, whereas in case of chicken tissues two phases of dissociation were discernible. Differences between Ka and the ratio of the association and dissociation rate constants are explained by non-equilibrium conditions. The stability of receptors from the two species differed significantly, the chick receptor being more stable. Hormone-receptor complex from each tissue could be separated into two fractions by DE-52 chromatography. The peak eluted at the lower KCl concentration in the case of chick corresponded to the fast dissociating hormone-receptor complex. Kinetic analyses proved to be just as useful as ion-exchange chromatography for the characterization of, and distinguishing between, glucocorticoid receptors.

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不同淋巴组织中胞浆糖皮质激素受体的理化性质。
对鸡和大鼠5种不同淋巴组织的细胞溶胶糖皮质激素受体进行了表征和理化参数比较。除了鸡组织的细胞质受体对地塞米松的特异性略高于大鼠组织的特异性外,两种受体的结合特异性相似。地塞米松受体复合物的结合速率常数在鸡胸腺和法氏囊中比在其他细胞质中高约一个数量级。在大鼠组织中,地塞米松受体复合物的解离发生在一个步骤中,而在鸡组织中,解离可分为两个阶段。非平衡条件解释了Ka与缔合速率常数和解离速率常数比值之间的差异。两种昆虫受体的稳定性差异显著,雏鸟受体更稳定。每个组织的激素受体复合物都可以通过DE-52色谱分离成两个部分。在鸡的情况下,低KCl浓度洗脱的峰对应于快速解离激素受体复合物。动力学分析被证明是一样有用的离子交换色谱表征,并区分,糖皮质激素受体。
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[Juvenile delinquency]. Analysis of Ca2+-induced K+-transport of human erythrocytes in propionate media. Is elastomucoproteinase a double-headed enzyme? Glucocorticoid receptor is activated by heparin and deactivated by plasmin. Sensitivity of thrombin and plasmin to heparin and antithrombin III.
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