The five Rs of glucocorticoid action during inflammation: ready, reinforce, repress, resolve, and restore

被引:268
作者
Busillo, John M. [1 ]
Cidlowski, John A. [1 ]
机构
[1] NIEHS, Lab Signal Transduct, NIH, US Dept HHS, Res Triangle Pk, NC 27709 USA
关键词
NF-KAPPA-B; INNATE IMMUNE-SYSTEM; CHROMATIN ACCESSIBILITY; RECEPTOR DIMERIZATION; DEHYDROGENASE TYPE-1; GENE-EXPRESSION; NUCLEAR; PHOSPHORYLATION; INHIBITION; CROSSTALK;
D O I
10.1016/j.tem.2012.11.005
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Glucocorticoids are essential for maintaining homeostasis and regulate a wide variety of physiological processes. Therapeutically, synthetic glucocorticoids are widely prescribed for the treatment of inflammation, autoimmune disorders, and malignancies of lymphoid origin. In this review we examine emerging evidence highlighting both proinflammatory and anti-inflammatory actions of glucocorticoids on both the innate and adaptive immune systems. We incorporate these findings into the more traditional anti-inflammatory role attributed to glucocorticoids, and propose how the two seemingly disparate processes seamlessly work together to resolve cellular responses to inflammatory stimuli. These ideas provide a framework by which glucocorticoids ready and reinforce the innate immune system, and repress the adaptive immune system, to help to resolve inflammation and restore homeostasis.
引用
收藏
页码:109 / 119
页数:11
相关论文
共 92 条
[1]
Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[2]
SERPINA3 (aka alpha-1-antichymotrypsin) [J].
Baker, Crystal ;
Belbin, Olivia ;
Kalsheker, Noor ;
Morgan, Kevin .
FRONTIERS IN BIOSCIENCE, 2007, 12 :2821-2835
[4]
Glucocorticoid therapy of antigen-induced arthritis depends on the dimerized glucocorticoid receptor in T cells [J].
Baschant, Ulrike ;
Frappart, Lucien ;
Rauchhaus, Una ;
Bruns, Lisa ;
Reichardt, Holger M. ;
Kamradt, Thomas ;
Braeuer, Rolf ;
Tuckermann, Jan P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (48) :19317-19322
[5]
Crosstalk in Inflammation: The Interplay of Glucocorticoid Receptor-Based Mechanisms and Kinases and Phosphatases [J].
Beck, Ilse M. E. ;
Vanden Berghe, Wim ;
Vermeulen, Linda ;
Yamamoto, Keith R. ;
Haegeman, Guy ;
De Bosscher, Karolien .
ENDOCRINE REVIEWS, 2009, 30 (07) :830-882
[6]
Macrophage glucocorticoid receptors regulate toll-like receptor 4-mediated inflammatory responses by selective inhibition of p38 MAP kinase [J].
Bhattacharyya, Sandip ;
Brown, Diane E. ;
Brewer, Judson A. ;
Vogt, Sherri K. ;
Muglia, Louis J. .
BLOOD, 2007, 109 (10) :4313-4319
[7]
Transcription Factor AP1 Potentiates Chromatin Accessibility and Glucocorticoid Receptor Binding [J].
Biddie, Simon C. ;
John, Sam ;
Sabo, Pete J. ;
Thurman, Robert E. ;
Johnson, Thomas A. ;
Schiltz, R. Louis ;
Miranda, Tina B. ;
Sung, Myong-Hee ;
Trump, Saskia ;
Lightman, Stafford L. ;
Vinson, Charles ;
Stamatoyannopoulos, John A. ;
Hager, Gordon L. .
MOLECULAR CELL, 2011, 43 (01) :145-155
[8]
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
[9]
T-cell glucocorticoid receptor is required to suppress COX-2-mediated lethal immune activation [J].
Brewer, JA ;
Khor, B ;
Vogt, SK ;
Muglia, LM ;
Fujiwara, H ;
Haegele, KE ;
Sleckman, BP ;
Muglia, LJ .
NATURE MEDICINE, 2003, 9 (10) :1318-1322
[10]
Glucocorticoid receptor-JNK interaction mediates inhibition of the JNK pathway by glucocorticoids [J].
Bruna, A ;
Nicolàs, M ;
Muñoz, A ;
Kyriakis, JM ;
Caelles, C .
EMBO JOURNAL, 2003, 22 (22) :6035-6044