## Abstract Human cells with osteogenic capacity were studied for differential gene expression. In the first part of the study we compared gene expression of marrow stroma cells (MSC) in comparison to matured osteoblasts cultured from trabecular bone (TBC) that were analyzed by RT‐PCR for series of
Hydrocortisone increases the rate of differentiation of cultured human osteoblasts
✍ Scribed by Deborah C. Ireland; Sharyn Bord; Siân R. Beavan; Juliet E. Compston
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 200 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0730-2312
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✦ Synopsis
Abstract
Reduced bone formation is the main finding in glucocorticoid‐induced osteoporosis. The aim of this study was to determine whether differentiation of cultured human osteoblasts is inhibited by high concentrations of hydrocortisone. We measured the levels of mRNAs for three markers of cellular differentiation, type 1 collagen (COL1), alkaline phosphatase (ALP), and osteocalcin (OC), in four lines of human osteoblasts from female donors cultured with doses of hydrocortisone from 0 μM to 4 μM. The change in ALP/COL1 mRNA ratio over a given time was used to determine the average rate of differentiation of the cells in a culture. Although basal expression profiles and their changes with time were different for the different cell lines, all cell lines showed a dose‐dependent rise in the rate of increase of ALP mRNA relative to COL1 mRNA. However, increase in OC mRNA with time, seen here only in young donor hOBs, was significantly inhibited by 4 μM hydrocortisone, indicating that hydrocortisone can inhibit OC expression while promoting cellular differentiation. The data suggest that increasing concentrations of glucocorticoid, including concentrations similar to plasma levels in patients receiving oral glucocorticoid therapy, increase the rate of cellular differentiation. © 2003 Wiley‐Liss, Inc.
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