Dexamethasone-induced expression of the glucocorticoid response gene lipocalin 2 in chondrocytes

Owen, Helen C., Roberts, S. J., Ahmed, S. F. and Farquharson, C. (2008) Dexamethasone-induced expression of the glucocorticoid response gene lipocalin 2 in chondrocytes. American journal of physiology. Endocrinology and metabolism, 294 (6). E1023-E1034. ISSN 0193-1849

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Abstract

Glucocorticoids (GC) are commonly used anti-inflammatory drugs, but long-term use can result in marked growth retardation in children due to their actions on growth plate chondrocytes. To gain an insight into the mechanisms involved in GC-induced growth retardation, we performed Affymetrix microarray analysis of the murine chondrogenic cell line ATDC5, incubated with 10(-6) M dexamethasone (Dex) for 24 h. Downregulated genes included secreted frizzled-related protein and IGF-I, and upregulated genes included serum/GC-regulated kinase, connective-tissue growth factor, and lipocalin 2. Lipocalin 2 expression increased 40-fold after 24-h Dex treatment. Expression increased further after 48-h (75-fold) and 96-h (84-fold) Dex treatment, and this response was Dex concentration dependent. Lipocalin 2 was immunolocalized to both proliferating and hypertrophic growth plate zones, and its expression was increased by Dex in primary chondrocytes at 6 h (3-fold, P < 0.05). The lipocalin 2 response was blocked by the GC-receptor antagonist RU-486 and was increased further by the protein synthesis blocker cycloheximide. Proliferation in lipocalin 2-overexpressing cells was less than in control cells (49%, P < 0.05), and overexpression caused an increase in collagen type X expression (4-fold, P < 0.05). The effects of lipocalin 2 overexpression on chondrocyte proliferation (64%, P < 0.05) and collagen type X expression (8-fold, P < 0.05) were further exacerbated with the addition of 10(-6) M Dex. This synergistic effect may be explained by a further increase in lipocalin 2 expression with Dex treatment of transfected cells (45%, P < 0.05). These results suggest that lipocalin 2 may mediate Dex effects on chondrocytes and provides a potential novel mechanism for GC-induced growth retardation.

Item Type: Article
Research Areas: A. > School of Science and Technology > Natural Sciences
Item ID: 19108
Useful Links:
Depositing User: Helen Roberts
Date Deposited: 20 Apr 2016 11:52
Last Modified: 30 May 2019 18:38
URI: https://eprints.mdx.ac.uk/id/eprint/19108

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