Cortisol resistance in the New World revisited

被引:36
作者
Fuller, PJ [1 ]
Smith, BJ [1 ]
Rogerson, FM [1 ]
机构
[1] Prince Henrys Inst Med Res, Clayton & Walter & Elizia Hall Inst, Parkville, Vic, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.tem.2004.07.001
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Insights into the molecular basis of glucocorticold action have been obtained from the analysis of cortisol resistance. The glucocorticoid receptor (GR) in both New World primates and guinea pigs has a decreased affinity, in vivo, for cortisol; this is achieved by two distinct mechanisms. In the New World primates recent studies have identified a key role for co-chaperones. The amino acids responsible for cortisol resistance in the guinea pig GR lie not in the ligand-binding pocket but on the surface of the receptor. We hypothesize that this region might be the site of interaction between the co-chaperones and the GR, and hence that the resistance occurs through the same mechanism, albeit from opposite sides.
引用
收藏
页码:296 / 299
页数:4
相关论文
共 31 条
[1]
Molecular determinants of glucocorticoid receptor function and tissue sensitivity to glucocorticoids [J].
Bamberger, CM ;
Schulte, HM ;
Chrousos, GP .
ENDOCRINE REVIEWS, 1996, 17 (03) :245-261
[2]
Crystal structure of the glucocorticoid receptor ligand binding domain reveals a novel mode of receptor dimerization and coactivator recognition [J].
Bledsoe, RK ;
Montana, VG ;
Stanley, TB ;
Delves, CJ ;
Apolito, CJ ;
McKee, DD ;
Consler, TG ;
Parks, DJ ;
Stewart, EL ;
Willson, TM ;
Lambert, MH ;
Moore, JT ;
Pearce, KH ;
Xu, HE .
CELL, 2002, 110 (01) :93-105
[3]
BRANDON DD, 1989, CANCER RES, V49, pS2203
[4]
INHIBITION OF DEXAMETHASONE BINDING TO HUMAN GLUCOCORTICOID RECEPTOR BY NEW-WORLD PRIMATE CELL-EXTRACTS [J].
BRANDON, DD ;
KENDALL, JW ;
ALMAN, K ;
TOWER, P ;
LORIAUX, DL .
STEROIDS, 1995, 60 (07) :463-466
[5]
PITUITARY-ADRENAL FUNCTION IN SQUIRREL-MONKEY [J].
BROWN, GM ;
GROTA, LJ ;
PENNEY, DP ;
REICHLIN, S .
ENDOCRINOLOGY, 1970, 86 (03) :519-&
[6]
Molecular chaperone interactions with steroid receptors: an update [J].
Cheung, J ;
Smith, DF .
MOLECULAR ENDOCRINOLOGY, 2000, 14 (07) :939-946
[7]
GLUCOCORTICOID HORMONE RESISTANCE DURING PRIMATE EVOLUTION - RECEPTOR-MEDIATED MECHANISMS [J].
CHROUSOS, GP ;
RENQUIST, D ;
BRANDON, D ;
EIL, C ;
PUGEAT, M ;
VIGERSKY, R ;
CUTLER, GB ;
LORIAUX, DL ;
LIPSETT, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (06) :2036-2040
[8]
TARGETED DISRUPTION OF THE GLUCOCORTICOID RECEPTOR GENE BLOCKS ADRENERGIC CHROMAFFIN CELL-DEVELOPMENT AND SEVERELY RETARDS LUNG MATURATION [J].
COLE, TJ ;
BLENDY, JA ;
MONAGHAN, AP ;
KRIEGLSTEIN, K ;
SCHMID, W ;
AGUZZI, A ;
FANTUZZI, G ;
HUMMLER, E ;
UNSICKER, K ;
SCHUTZ, G .
GENES & DEVELOPMENT, 1995, 9 (13) :1608-1621
[9]
Squirrel monkey immunophilin FKBP51 is a potent inhibitor of glucocorticoid receptor binding [J].
Denny, WB ;
Valentine, DL ;
Reynolds, PD ;
Smith, DF ;
Scammell, JG .
ENDOCRINOLOGY, 2000, 141 (11) :4107-4113
[10]
Molecular chaperones function as steroid receptor nuclear mobility factors [J].
Elbi, C ;
Walker, DA ;
Romero, G ;
Sullivan, WP ;
Toft, DO ;
Hager, GL ;
DeFranco, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2876-2881