Selective conversion by microglia of dehydroepiandrosterone to 5-androstenediol - A steroid with inherent estrogenic properties

被引:29
作者
Jellinck, Peter H.
Kaufmann, Martin
Gottfried-Blackmore, Andres
McEwen, Bruce S.
Jones, Glenville
Bulloch, Karen
机构
[1] Rockefeller Univ, Cellular Physiol & Immunol Lab, New York, NY 10021 USA
[2] Queens Univ, Dept Biochem, Kingston, ON K7L 3N6, Canada
[3] Rockefeller Univ, Harold & Margaret Milliken Hatch, Neuroendocrinol Lab, New York, NY 10021 USA
关键词
microglia; DHEA; 5-androstenediol; estrogen;
D O I
10.1016/j.jsbmb.2007.04.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The well-established neuroprotective effect of dehydroepiandrosterone (DHEA) has been attributed to its metabolism in the brain to provide estrogens known to be neuroprotective and to enhance memory and learning in humans and animals. However, our previous work showed that the conversion of DHEA to 4-androstenedione (AD), the precursor of estrone (E-1) and estradiol (E-2), is very low in several different types of neural cells, and that the main product is 7 alpha-hydroxy-DHEA (7 alpha-OH-DHEA). In this study, we found that microglia are an exception and produce mainly 5-androstene-3 beta,17 beta-diol (Delta(5)-Adiol), a C-19 steroid with estrogen-like activity from DHEA. Virtually, no other products, including testosterone (T) were detected by TLC or HPLC in incubations of H-3-labeled DHEA with the BV2 microglial cell line. Microglia are important brain cells that are thought to play a house-keeping role during the steady state, and that are crucial to the brain's immune reaction to injury and the heating process. Our findings suggest that the microglia-produced Delta(5)-Adiol might have a role in modulating estrogen-sensitive neuroplastic events in the brain, in the absence of adequate local synthesis of estrone and estradiol. (C) 2007 Published by Elsevier Ltd.
引用
收藏
页码:156 / 162
页数:7
相关论文
共 40 条
[1]   Migration and differentiation of neural precursor cells can be directed by microglia [J].
Aarum, J ;
Sandberg, K ;
Haeberlein, SLB ;
Persson, MAA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15983-15988
[2]   CONTROL OF SECRETION AND THE FUNCTION OF C-19-DELTA-5-STEROIDS OF THE HUMAN ADRENAL-GLAND [J].
ADAMS, JB .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1985, 41 (01) :1-17
[3]   ASTROCYTES AND NEUROSTEROIDS - METABOLISM OF PREGNENOLONE AND DEHYDROEPIANDROSTERONE - REGULATION BY CELL-DENSITY [J].
AKWA, Y ;
SANANES, N ;
GOUEZOU, M ;
ROBEL, P ;
BAULIEU, EE ;
LEGOASCOGNE, C .
JOURNAL OF CELL BIOLOGY, 1993, 121 (01) :135-143
[4]  
Baulieu E. E., 1991, NEUROSTEROIDS BRAIN, P63
[5]   Neuroprotection against oxidative stress by estrogens: Structure-activity relationship [J].
Behl, C ;
Skutella, T ;
Lezoualch, F ;
Post, A ;
Widmann, M ;
Newton, CJ ;
Holsboer, F .
MOLECULAR PHARMACOLOGY, 1997, 51 (04) :535-541
[6]   ENZYMIC FORMATION OF 3BETA-HYDROXYANDROST-4-EN-17-ONE [J].
BREUER, H ;
NORYMBERSKI, JK ;
DAHM, K .
JOURNAL OF ENDOCRINOLOGY, 1963, 27 (03) :357-&
[7]   NEW METHOD FOR ESTABLISHMENT OF NEURONAL CELL LINES FROM MOUSE-BRAIN [J].
BULLOCH, K ;
STALLCUP, WB ;
COHN, M .
LIFE SCIENCES, 1978, 22 (06) :495-504
[8]   DERIVATION AND CHARACTERIZATION OF NEURONAL CELL LINES FROM RAT AND MOUSE-BRAIN [J].
BULLOCH, K ;
STALLCUP, WB ;
COHN, M .
BRAIN RESEARCH, 1977, 135 (01) :25-36
[9]   STEROIDOGENIC ENZYME P450C17 IS EXPRESSED IN THE EMBRYONIC CENTRAL-NERVOUS-SYSTEM [J].
COMPAGNONE, NA ;
BULFONE, A ;
RUBENSTEIN, JLR ;
MELLON, SH .
ENDOCRINOLOGY, 1995, 136 (11) :5212-5223
[10]   EVIDENCE AND CHARACTERIZATION OF THE BINDING OF 2 H-3-LABELED ANDROGENS TO THE ESTROGEN-RECEPTOR [J].
GARCIA, M ;
ROCHEFORT, H .
ENDOCRINOLOGY, 1979, 104 (06) :1797-1804