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钙对肝脏糖皮质激素受体的影响。

The effect of calcium on the hepatic glucocorticoid receptor.

作者信息

Kalimi M, Hubbard J, Ray A

出版信息

J Steroid Biochem. 1983 Jun;18(6):665-71. doi: 10.1016/0022-4731(83)90244-3.

Abstract

The unbound glucocorticoid receptor of rat hepatic cytosol was very unstable at 25 degrees C. This receptor instability was increased by the addition of 1-10 mM Ca2+ such that the unbound glucocorticoid receptor was completely inactivated within 30 min at 25 degrees C in the presence of 5 mM Ca2+. Interestingly, Ca2+ inactivation was blocked approximately 80% by simultaneous addition of either 10 mM molybdate or 10 mM molybdate plus 5 mM dithiothreitol. Ten millimolar leupeptin or 10 mM alpha 2-macroglobulin did not inhibit Ca2+ inactivation of the receptor. In fact, leupeptin alone slightly inactivated the receptor. Prior treatment of cytosol with 10 mM molybdate plus 5 mM DTT at 25 degrees C for 30 min offered a complete protection against the subsequent addition of 5 mM Ca2+. The effects of Ca2+ were found to be irreversible since addition of molybdate or molybdate plus dithiothreitol after 5 mM Ca2+ treatment (20 min for 25 degrees C) did not reactivate partially inactivated receptors but did stabilize the remaining receptor binding at the time of molybdate or molybdate plus dithiothreitol addition. Addition of 1-5 mM Ca2+ to preformed [3H]-dexamethasone--receptor complexes slightly inhibited steroid--receptor complex transformation into a nuclear binding form at 25 degrees C. In addition, 10 mM Ca2+ altered the agarose gel filtration profile of the complex. Control cytosol or cytosol treated with 10 mM EDTA or 10 mM leupeptin showed three distinct macromolecular bound radioactivity peaks having Stokes radii of 65, 40 and 20 A. On the other hand, Ca2+-treated cytosol showed a single large aggregated component which was excluded in the void volume of the column. Trypsin (0.5 microgram/ml) generated a small steroid--receptor fragment of 20 A when added alone, but interestingly when added with 10 mM Ca2+ the [3H]-dexamethasone--receptor complex eluted in the agarose gel exclusion volume. These results show that Ca2+ has a profound effect on rat hepatic glucocorticoid receptors and that molybdate can block Ca2+-dependent receptor inactivation.

摘要

大鼠肝细胞溶质中的未结合糖皮质激素受体在25℃时非常不稳定。添加1 - 10 mM Ca2+会加剧这种受体的不稳定性,以至于在5 mM Ca2+存在的情况下,25℃时未结合的糖皮质激素受体在30分钟内完全失活。有趣的是,同时添加10 mM钼酸盐或10 mM钼酸盐加5 mM二硫苏糖醇可使Ca2+介导的失活被大约80%阻断。10 mM亮抑酶肽或10 mMα2 -巨球蛋白不会抑制受体的Ca2+介导的失活。事实上,单独的亮抑酶肽会使受体稍有失活。在25℃用10 mM钼酸盐加5 mM二硫苏糖醇对细胞溶质进行预处理30分钟,可完全保护其免受随后添加的5 mM Ca2+的影响。发现Ca2+的作用是不可逆的,因为在5 mM Ca2+处理后(25℃处理20分钟)添加钼酸盐或钼酸盐加二硫苏糖醇不会使部分失活的受体重新激活,但在添加钼酸盐或钼酸盐加二硫苏糖醇时会稳定剩余的受体结合。向预先形成的[3H] - 地塞米松 - 受体复合物中添加1 - 5 mM Ca2+会在25℃时轻微抑制类固醇 - 受体复合物转化为核结合形式。此外,10 mM Ca2+改变了复合物的琼脂糖凝胶过滤图谱。对照细胞溶质或用10 mM EDTA或10 mM亮抑酶肽处理的细胞溶质显示出三个不同的大分子结合放射性峰,其斯托克斯半径分别为65、40和20 Å。另一方面,经Ca2+处理的细胞溶质显示出一个单一的大聚集成分,它被排除在柱的空体积中。单独添加胰蛋白酶(0.5微克/毫升)会产生一个20 Å的小类固醇 - 受体片段,但有趣的是,当与10 mM Ca2+一起添加时,[3H] - 地塞米松 - 受体复合物在琼脂糖凝胶排阻体积中洗脱。这些结果表明,Ca2+对大鼠肝脏糖皮质激素受体有深远影响,并且钼酸盐可以阻断Ca2+依赖的受体失活。

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