Kim Hyongbum, Lee Jung Min, Park Jae Sun, Jo Sangmee Ahn, Kim Yong-Ou, Kim Chan-Wha, Jo Inho
Department of Biomedical Sciences, National Institute of Health, Seoul, South Korea.
Biochem Biophys Res Commun. 2008 Jul 18;372(1):243-8. doi: 10.1016/j.bbrc.2008.05.025. Epub 2008 May 15.
Glucocorticoids stabilize the blood-brain barrier (BBB), leading to attenuation of vasogenic brain edema. However, the action mechanism of glucocorticoids has been poorly elucidated. To elucidate the mechanism, we investigated whether dexamethasone (Dex), a synthetic glucocorticoid hormone, regulates the levels of key permeability regulating factors such as angiopoietin-1, angiopoietin-2, and vascular endothelial growth factor (VEGF) in the three types of cells comprising BBB. Dex increased the level of angiopoietin-1 mRNA and protein and decreased VEGF mRNA and protein in brain astrocytes and pericytes, but not in endothelial cells. The mRNA and protein of angiopoietin-2 were detected only in endothelial cells and not regulated by Dex. The Dex-induced regulation of angiopoietin-1 and VEGF was inhibited by RU486, suggestive of glucocorticoid receptor mediation. The mRNA stability of angiopoietin-1 and VEGF was not changed by Dex treatment, implying that Dex increases angiopoietin-1 and decreases VEGF through transcriptional regulation. This is the first study showing the coordinate regulation of angiopoietin-1 and VEGF by glucocorticoids, suggesting a novel mechanism underlying glucocorticoids-induced stabilization of BBB.
糖皮质激素可稳定血脑屏障(BBB),从而减轻血管源性脑水肿。然而,糖皮质激素的作用机制尚未完全阐明。为了阐明其机制,我们研究了合成糖皮质激素地塞米松(Dex)是否能调节构成血脑屏障的三种细胞中关键通透性调节因子的水平,如血管生成素-1、血管生成素-2和血管内皮生长因子(VEGF)。Dex可增加脑星形胶质细胞和周细胞中血管生成素-1的mRNA和蛋白水平,并降低VEGF的mRNA和蛋白水平,但对内皮细胞无此作用。血管生成素-2的mRNA和蛋白仅在内皮细胞中检测到,且不受Dex调节。RU486可抑制Dex诱导的血管生成素-1和VEGF的调节,提示糖皮质激素受体介导此过程。Dex处理未改变血管生成素-1和VEGF的mRNA稳定性,这意味着Dex通过转录调节增加血管生成素-1并降低VEGF。这是第一项显示糖皮质激素对血管生成素-1和VEGF进行协同调节的研究,提示了糖皮质激素诱导血脑屏障稳定的新机制。