Gu Feng, Hata Ryuji, Toku Kazuko, Yang Lihua, Ma Yong-Jie, Maeda Nobuji, Sakanaka Masahiro, Tanaka Junya
Department of Anatomy, Ehime University School of Medicine, Shigenobu, Ehime, Japan.
J Neurosci Res. 2003 Jun 15;72(6):709-15. doi: 10.1002/jnr.10603.
Aquaporin-4 (AQP4) is located on astrocyte endfeet that face blood vessels in the brain and in the pia. It is thought to play a crucial role in the development of brain edema. To confirm the notion that sex steroids and dexamethasone influence brain edema through AQP4 regulation, we investigated the effects of 17beta-estradiol, testosterone, and dexamethasone on the expression of AQP4 in cultured astrocytes. Testosterone significantly up-regulated AQP4 at the level of both protein and mRNA. At a concentration of 100 nM, testosterone significantly increased AQP4 protein levels and ameliorated the osmotic fragility of astrocytes from hypoosmotic stress, suggesting that the increased levels of AQP4 facilitated the testosterone function. Moreover, this effect was attenuated by the protein kinase C activator 12-O-tetradecanoylphorbol 13-acetate, which can rapidly decrease AQP4 mRNA expression, indicating that the response was specific. These results indicate that AQP4 can alter the osmotic fragility of astrocytes and that testosterone can influence brain edema through AQP4 regulation, whereas 17beta-estradiol and dexamethasone cannot.
水通道蛋白4(AQP4)位于面向脑内血管和软脑膜的星形胶质细胞终足上。它被认为在脑水肿的发展中起关键作用。为了证实性类固醇和地塞米松通过AQP4调节影响脑水肿这一观点,我们研究了17β-雌二醇、睾酮和地塞米松对培养星形胶质细胞中AQP4表达的影响。睾酮在蛋白质和mRNA水平上均显著上调AQP4。在100 nM浓度下,睾酮显著增加AQP4蛋白水平,并改善了星形胶质细胞在低渗应激下的渗透脆性,表明AQP4水平的升高促进了睾酮的作用。此外,蛋白激酶C激活剂12-O-十四酰佛波醇13-乙酸酯可减弱这种效应,该激活剂可迅速降低AQP4 mRNA表达,表明该反应具有特异性。这些结果表明,AQP4可改变星形胶质细胞的渗透脆性,睾酮可通过AQP4调节影响脑水肿,而17β-雌二醇和地塞米松则不能。