Testosterone up-regulates aquaporin-4 expression in cultured astrocytes

被引:54
作者
Gu, F
Hata, R
Toku, K
Yang, LH
Ma, YJ
Maeda, N
Sakanaka, M
Tanaka, J
机构
[1] Ehime Univ, Sch Med, Dept Physiol, Shigenobu, Ehime 7910295, Japan
[2] Ehime Univ, Sch Med, Dept Anat, Shigenobu, Ehime 7910295, Japan
关键词
aquaporin; astrocyte; testosterone; 17; beta-estradiol; dexamethasone; MESSENGER-RNA EXPRESSION; PROTEIN-KINASE-C; ANDROGEN RECEPTOR; BRAIN EDEMA; GROWTH-FACTOR; IN-VITRO; DEXAMETHASONE; RAT; ACTIVATION; HYPONATREMIA;
D O I
10.1002/jnr.10603
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:709 / 715
页数:7
相关论文
共 43 条
[1]   Aquaporins in brain: Distribution, physiology, and pathophysiology [J].
Badaut, T ;
Lasbennes, T ;
Magistretti, PJ ;
Regli, L .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2002, 22 (04) :367-378
[2]   Androgen receptor phosphorylation [J].
Blok, LJ ;
deRuiter, PE ;
Brinkmann, AO .
ENDOCRINE RESEARCH, 1996, 22 (03) :197-219
[3]   STIMULATION OF TUMOR-NECROSIS-FACTOR-ALPHA PRODUCTION BY MYCOPLASMAS AND INHIBITION BY DEXAMETHASONE IN CULTURED ASTROCYTES [J].
BRENNER, T ;
YAMIN, A ;
ABRAMSKY, O ;
GALLILY, R .
BRAIN RESEARCH, 1993, 608 (02) :273-279
[4]  
CULIG Z, 1994, CANCER RES, V54, P5474
[5]   Phorbol ester causes ligand-independent activation of the androgen receptor [J].
Darne, C ;
Veyssiere, G ;
Jean, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 256 (03) :541-549
[6]  
DERIJK R, 1994, ANN NY ACAD SCI, V746, P33
[7]   Molecular biology of the androgen receptor: From molecular understanding to the clinic [J].
Eder, IE ;
Culig, Z ;
Putz, T ;
Nessler-Menardi, C ;
Bartsch, G ;
Klocker, H .
EUROPEAN UROLOGY, 2001, 40 (03) :241-251
[8]   Protein kinase C pathway potentiates androgen-mediated gene expression of the mouse vas deferens specific aldose reductase-like protein (MVDP) [J].
Fabre, S ;
Darne, C ;
Veyssiere, G ;
Jean, C .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1996, 124 (1-2) :79-86
[9]   In vitro effects of dexamethasone on hypoxia-induced hyperpermeability and expression of vascular endothelial growth factor [J].
Fischer, S ;
Renz, D ;
Schaper, W ;
Karliczek, GF .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 411 (03) :231-243
[10]  
HASEGAWA H, 1994, J BIOL CHEM, V269, P5497