MOLECULAR ACTIONS OF GLUCOCORTICOIDS IN CARTILAGE AND BONE DURING HEALTH, DISEASE, AND STEROID THERAPY

被引:170
作者
Hartmann, Kerstin
Koenen, Mascha
Schauer, Sebastian
Wittig-Blaich, Stephanie
Ahmad, Mubashir
Baschant, Ulrike
Tuckermann, Jan P.
机构
[1] Univ Ulm, Inst Comparat Mol Endocrinol, D-89081 Ulm, Germany
[2] Tech Univ Dresden, Div Endocrinol Diabet & Bone Dis, Dept Med 3, D-01062 Dresden, Germany
关键词
INDUCED LEUCINE-ZIPPER; HEAT-SHOCK-PROTEIN; EARLY RHEUMATOID-ARTHRITIS; ANTIGEN-INDUCED ARTHRITIS; K-DEPENDENT CARBOXYLASE; MESENCHYMAL STEM-CELLS; MATRIX GLA PROTEIN; 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1; RABBIT COSTAL CHONDROCYTES; INDUCED INSULIN-RESISTANCE;
D O I
10.1152/physrev.00011.2015
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Cartilage and bone are severely affected by glucocorticoids (GCs), steroid hormones that are frequently used to treat inflammatory diseases. Major complications associated with long-term steroid therapy include impairment of cartilaginous bone growth and GC-induced osteoporosis. Particularly in arthritis, GC application can increase joint and bone damage. Contrarily, endogenous GC release supports cartilage and bone integrity. In the last decade, substantial progress in the understanding of the molecular mechanisms of GC action has been gained through genome-wide binding studies of the GC receptor. These genomic approaches have revolutionized our understanding of gene regulation by ligand-induced transcription factors in general. Furthermore, specific inactivation of GC signaling and the GC receptor in bone and cartilage cells of rodent models has enabled the cell-specific effects of GCs in normal tissue homeostasis, inflammatory bone diseases, and GC-induced osteoporosis to be dissected. In this review, we summarize the current view of GC action in cartilage and bone. We further discuss future research directions in the context of new concepts for optimized steroid therapies with less detrimental effects on bone.
引用
收藏
页码:409 / 447
页数:39
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