Androgen receptor immunoreactivity in forebrain axons and dendrites in the rat

被引:66
作者
DonCarlos, LL
Garcia-Ovejero, D
Sarkey, S
Garcia-Segura, LM
Azcoitia, I
机构
[1] Loyola Univ, Stritch Sch Med, Dept Cell Biol Neurobiol & Anat, Maywood, IL 60153 USA
[2] CSIC, Inst Cajal, E-28002 Madrid, Spain
[3] Loyola Univ, Stritch Sch Med, Program Neurosci, Maywood, IL 60153 USA
[4] Univ Complutense Madrid, Dept Biol Celular, Madrid, Spain
关键词
D O I
10.1210/en.2002-0105
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As members of the steroid receptor superfamily, androgen receptors (ARs) have been traditionally identified as transcription factors. In the presence of ligand, ARs reside in the nucleus, where, upon ligand binding, the receptors dimerize and bind to specific response elements in the promoter region of hormone-responsive genes. However, in this report, we describe the discovery that ARs are also present in axons and dendrites within the mammalian central nervous system. AR expression in axons was identified in the rat brain at the light microscopic level using two different antibodies directed against the N terminus of the AR protein and nickel intensified 3'-3'-diaminobenzidine, and also using fluorescence methods and confocal microscopy. This distribution was confirmed at the ultrastructural level. In addition, AR immunoreactivity was identified in small dendrites at the ultrastructural level. AR-immunoreactive axons were observed primarily in the cerebral cortex and were rare in regions where nuclear AR expression is abundant. The observation that ARs are present in axons and dendrites highlights the possibility that androgens play an important and novel extranuclear role in neuronal function.
引用
收藏
页码:3632 / 3638
页数:7
相关论文
共 52 条
[1]  
Adams MM, 2002, J NEUROSCI, V22, P3608
[2]   Testosterone protects cerebellar granule cells from oxidative stress-induced cell death through a receptor mediated mechanism [J].
Ahlbom, E ;
Prins, GS ;
Ceccatelli, S .
BRAIN RESEARCH, 2001, 892 (02) :255-262
[3]   GONADAL-STEROID INDUCTION OF STRUCTURAL SEX-DIFFERENCES IN THE CENTRAL NERVOUS-SYSTEM [J].
ARNOLD, AP ;
GORSKI, RA .
ANNUAL REVIEW OF NEUROSCIENCE, 1984, 7 :413-442
[4]   Quantitative estimation of estrogen and androgen receptor-immunoreactive cells in the forebrain of neonatally estrogen-deprived male rats [J].
Bakker, J ;
Pool, CW ;
Sonnemans, M ;
vanLeeuwen, FW ;
Slob, AK .
NEUROSCIENCE, 1997, 77 (03) :911-919
[5]   CYTOPLASMIC ESTROGEN-RECEPTORS IN RAT-BRAIN - IMMUNOCYTOCHEMICAL EVIDENCE USING 3 ANTIBODIES WITH DISTINCT EPITOPES [J].
BLAUSTEIN, JD .
ENDOCRINOLOGY, 1992, 131 (03) :1336-1342
[6]   ESTROGEN-RECEPTORS IN DENDRITES AND AXON TERMINALS IN THE GUINEA-PIG HYPOTHALAMUS [J].
BLAUSTEIN, JD ;
LEHMAN, MN ;
TURCOTTE, JC ;
GREENE, G .
ENDOCRINOLOGY, 1992, 131 (01) :281-290
[7]  
BREEDLOVE SM, 1992, J NEUROSCI, V12, P4133
[8]  
Brooks BP, 1998, J NEUROCHEM, V70, P1054
[9]   Perimembrane localization of the estrogen receptor α protein in neuronal processes of cultured hippocampal neurons [J].
Clarke, CH ;
Norfleet, AM ;
Clarke, MSF ;
Watson, CS ;
Cunningham, KA ;
Thomas, ML .
NEUROENDOCRINOLOGY, 2000, 71 (01) :34-42
[10]   DIFFERENTIAL EXPRESSION OF THE MOUSE MITOCHONDRIAL GENES AND THE MITOCHONDRIAL RNA-PROCESSING ENDORIBONUCLEASE RNA BY ANDROGENS [J].
CORNWALL, GA ;
ORGEBINCRIST, MC ;
HANN, SR .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (07) :1032-1042