Neuronal differentiation of PC12 cells abolishes the expression of membrane androgen receptors

被引:10
作者
Alexaki, Vassilia-Ismini
Dermitzaki, Eirini
Charalampopoulos, Ioannis
Kampa, Marilena
Nifli, Artemissia-Phoebe
Gravanis, Achille
Margioris, Andrew N.
Castanas, Elias
机构
[1] Univ Crete, Sch Med, Lab Expt Endocrinol, Iraklion 71003, Greece
[2] Univ Crete, Sch Med, Lab Clin Chem Biochem, GR-71003 Iraklion, Greece
[3] Univ Crete, Sch Med, Pharmacol Lab, GR-71003 Iraklion, Greece
关键词
PC12; cells; testosterone; membrane binding sites (androgen); apoptosis; catecholamines; (nor-epinephrine; dopamine);
D O I
10.1016/j.yexcr.2006.04.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sex steroids affect adrenal chromaffin cell function. In the present work, we have examined the expression and functional significance of membrane androgen receptor sites in normal rat adrenal chromaffin cells and in the PC12 rat pheochromocytoma cell line which can differentiate to either a neuronal or to an epithelial phenotype and expresses membrane estrogen receptor sites. Our data are as follows: (a) no cytosolic androgen receptors were found in both normal chromaffin and PC12 cells; (b) both types of chromaffin cells expressed high affinity membrane testosterone binding sites; (c) activation of these sites increased cytosolic Ca2+, decreased catecholamine secretion and induced apoptosis; (d) NGF-induced neuronal differentiation of PC12 cells resulted in the suppression of the number of membrane testosterone sites. In conclusion, our data provide evidence for the existence of specific membrane testosterone receptors on adrenal chromaffin cells via which androgens, (some of them originating in the cortex) modulate their function. Neuronal differentiation of chromaffin cells results in a significant attenuation of these effects, via suppression of the expression of membrane androgen receptors suggesting, that the latter are specific for epithelioid chromaffin cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:2745 / 2756
页数:12
相关论文
共 73 条
[1]   Activation of membrane estrogen receptors induce pro-survival kinases [J].
Alexaki, VI ;
Charalampopoulos, I ;
Kampa, M ;
Nifli, AP ;
Hatzoglou, A ;
Gravanis, A ;
Castanas, E .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2006, 98 (2-3) :97-110
[2]   Estrogen exerts neuroprotective effects via membrane estrogen receptors and rapid Akt/NOS activation [J].
Alexaki, VI ;
Charalampopoulos, I ;
Kampa, M ;
Vassalou, H ;
Theodoropoulos, P ;
Stathopoulos, EN ;
Hatzoglou, A ;
Gravanis, A ;
Castanas, E .
FASEB JOURNAL, 2004, 18 (11) :1594-+
[3]  
BAIZER L, 1985, J NEUROSCI, V5, P1176
[4]   NERVE GROWTH-FACTOR INDUCES SENSITIVITY TO BOTULINUM NEUROTOXIN TYPE-A IN NOREPINEPHRINE-SECRETING PC12 CELLS [J].
BANERJEE, A ;
MARTIN, TFJ ;
DASGUPTA, BR .
NEUROSCIENCE LETTERS, 1993, 164 (1-2) :93-96
[5]   Testosterone induces Ca2+ influx via non-genomic surface receptors in activated T cells [J].
Benten, WPM ;
Lieberherr, M ;
Sekeris, CE ;
Wunderlich, F .
FEBS LETTERS, 1997, 407 (02) :211-214
[6]   Functional testosterone receptors in plasma membranes of T cells [J].
Benten, WPM ;
Lieberherr, M ;
Giese, G ;
Wrehlke, C ;
Stamm, O ;
Sekeris, CE ;
Mossmann, H ;
Wunderlich, F .
FASEB JOURNAL, 1999, 13 (01) :123-133
[7]   Rapid effects of androgens in macrophages [J].
Benten, WPM ;
Guo, Z ;
Krücken, J ;
Wunderlich, F .
STEROIDS, 2004, 69 (8-9) :585-590
[8]   Heterogeneity in cytosolic calcium responses to hypoxia in carotid body cells [J].
Bright, GR ;
Agani, FH ;
Haque, U ;
Overholt, JL ;
Prabhakar, NR .
BRAIN RESEARCH, 1996, 706 (02) :297-302
[9]   Estrogen attenuates cell death induced by carboxy-terminal fragment of amyloid precursor protein in PC12 through a receptor-dependent pathway [J].
Chae, HS ;
Bach, JH ;
Lee, MW ;
Kim, HS ;
Kim, YS ;
Kim, KY ;
Choo, KY ;
Choi, SH ;
Park, CH ;
Lee, SH ;
Suh, YH ;
Kim, SS ;
Lee, WB .
JOURNAL OF NEUROSCIENCE RESEARCH, 2001, 65 (05) :403-407
[10]   G protein-associated, specific membrane binding sites mediate the neuroprotective effect of dehydroepiandrosterone [J].
Charalampopoulos, I ;
Alexaki, VI ;
Lazaridis, I ;
Dermitzaki, E ;
Avlonitis, N ;
Tsatsanis, C ;
Calogeropoulou, T ;
Margioris, AN ;
Castanas, E ;
Gravanis, A .
FASEB JOURNAL, 2006, 20 (01) :577-+