Kim Yoon Suk, Kim Jeonghan, Kim Yoonseo, Lee Young Han, Kim Jae-Hong, Lee Seung-Jae, Shin Soon Young, Ko Jesang
Department of Biomedical Laboratory Science, College of Health Science, Yonsei University, Wonju 222-701, South Korea.
Biochem Biophys Res Commun. 2008 Sep 19;374(2):373-7. doi: 10.1016/j.bbrc.2008.07.040. Epub 2008 Jul 18.
The glucocorticoid receptor (GR) is a ligand-activated transcription factor that mediates the effects of glucocorticoids in diverse cellular processes, including homeostasis, stress response, and inflammation. Glucocorticoids induce down-regulation of GR at both the mRNA and protein levels, causing reduced hormone responsiveness in response to long-term treatment with glucocorticoid. However, the mechanism involved in this process is still obscure. In this study, we examined whether calpain, a calcium-activated cysteine protease, is involved in ligand-stimulated degradation of GR. In COS-7 cells expressing the human GR, treatment with a calpain inhibitor abolished glucocorticoid-induced down-regulation of GR in a dose dependent manner. The protein level of endogenous GR was also elevated by inhibition of the calpain activity in HeLa cells treated with glucocorticoid. Furthermore, glucocorticoid-induced transcriptional activation of GR was enhanced in cells treated with a calpain inhibitor. These results indicate that calpain is involved in ligand-dependent degradation of GR, thus causing reduced hormone responsiveness.
糖皮质激素受体(GR)是一种配体激活的转录因子,介导糖皮质激素在多种细胞过程中的作用,包括体内平衡、应激反应和炎症。糖皮质激素在mRNA和蛋白质水平上均诱导GR下调,导致长期使用糖皮质激素治疗时激素反应性降低。然而,这一过程涉及的机制仍不清楚。在本研究中,我们检测了钙蛋白酶(一种钙激活的半胱氨酸蛋白酶)是否参与配体刺激的GR降解。在用人类GR表达的COS-7细胞中,用钙蛋白酶抑制剂处理以剂量依赖的方式消除了糖皮质激素诱导的GR下调。在用糖皮质激素处理的HeLa细胞中,抑制钙蛋白酶活性也提高了内源性GR的蛋白质水平。此外,在用钙蛋白酶抑制剂处理的细胞中,糖皮质激素诱导的GR转录激活增强。这些结果表明,钙蛋白酶参与了GR的配体依赖性降解,从而导致激素反应性降低。