Spencer R L, Kalman B A, Cotter C S, Deak T
Department of Psychology, Campus Box 345, University of Colorado, Boulder, CO 80309, USA.
Brain Res. 2000 Jun 23;868(2):275-86. doi: 10.1016/s0006-8993(00)02341-6.
These studies investigated autoregulation of glucocorticoid receptor (GR) protein expression and activation in rat brain using western blot methodology. By comparing GR immunoblot reactivity present in various tissue subcellular preparations we were able to discriminate between corticosterone-induced changes in GR activation or GR protein expression. Our cytosolic tissue preparation yielded a similar pattern of treatment effects on relative GR as measured by receptor binding assay or western blot. In both cases, short-term adrenalectomy (18 h) produced no change in cytosolic GR. On the other hand, long-term adrenalectomy (3-14 days) resulted in a large increase in cytosolic GR, whereas acute (1-2 h) treatment with high dose corticosterone produced a large decrease in cytosolic GR. Western blot measurement of GR levels in a nuclear extract or whole-cell extract from the same brains indicated that acute corticosterone treatment produced a large increase in nuclear GR and no change in whole-cell GR. Thus, all of the decrease in cytosolic GR observed after acute corticosterone treatment could be accounted for by receptor redistribution to the nuclear tissue fraction as opposed to rapid receptor protein downregulation. Long-term treatment of rats with adrenalectomy or high dose corticosterone produced a large increase and decrease, respectively, in whole-cell GR, indicating genuine changes in receptor protein expression. These studies indicate that in vivo regulation of GR protein expression in the rat brain can be studied using western blot analysis of a whole-cell tissue preparation. This procedure has an important advantage over receptor binding studies in that GR protein expression can be measured in adrenal-intact rats. These studies also support the validity of using cytosolic receptor binding assays to estimate relative changes in GR occupation/activation when appropriate comparison groups are included.
这些研究使用蛋白质印迹法研究了大鼠脑中糖皮质激素受体(GR)蛋白表达的自动调节及其激活情况。通过比较各种组织亚细胞制剂中GR免疫印迹反应性,我们能够区分皮质酮诱导的GR激活或GR蛋白表达的变化。我们的胞质组织制剂对相对GR产生的处理效应模式,与通过受体结合测定或蛋白质印迹法测得的结果相似。在这两种情况下,短期肾上腺切除术(18小时)并未使胞质GR发生变化。另一方面,长期肾上腺切除术(3 - 14天)导致胞质GR大幅增加,而高剂量皮质酮的急性(1 - 2小时)处理则使胞质GR大幅减少。对来自相同大脑的核提取物或全细胞提取物中GR水平进行蛋白质印迹测量表明,急性皮质酮处理使核GR大幅增加,而全细胞GR没有变化。因此,急性皮质酮处理后观察到的胞质GR的所有减少,都可归因于受体重新分布到核组织部分,而不是受体蛋白的快速下调。用肾上腺切除术或高剂量皮质酮对大鼠进行长期处理,分别使全细胞GR大幅增加和减少,表明受体蛋白表达发生了真正的变化。这些研究表明,使用全细胞组织制剂的蛋白质印迹分析,可以研究大鼠脑中GR蛋白表达的体内调节。该方法相对于受体结合研究具有重要优势,即可以在肾上腺完整的大鼠中测量GR蛋白表达。这些研究还支持在纳入适当比较组时,使用胞质受体结合测定来估计GR占据/激活的相对变化的有效性。