Up-regulation of inhibitors of DNA binding/differentiation gene during alendronate-induced osteoblast differentiationopen access
- Authors
- Kang, Ae Ra; Oh, Young Rim; Kim, Heung Yeol; Park, Min Jung; Joo, Bo Sun; Choi, Won Jun; Lee, Ji Young; Jung, Min Hyung; Ji, Yong Il; Choi, Jong Soon
- Issue Date
- May-2012
- Publisher
- SPRINGER HEIDELBERG
- Keywords
- Alendronate; Osteoblasts; Osteoporosis
- Citation
- ARCHIVES OF GYNECOLOGY AND OBSTETRICS, v.285, no.5, pp 1331 - 1338
- Pages
- 8
- Indexed
- SCIE
SCOPUS
- Journal Title
- ARCHIVES OF GYNECOLOGY AND OBSTETRICS
- Volume
- 285
- Number
- 5
- Start Page
- 1331
- End Page
- 1338
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/22186
- DOI
- 10.1007/s00404-011-2141-1
- ISSN
- 0932-0067
1432-0711
- Abstract
- To investigate the effect of alendronate on the expression of Id genes in osteoblast differentiation. C2C12 cells were treated with alendronate for various concentrations and time periods. For evaluation of alendronate-induced osteoblast differentiation in C2C12 cells, alkaline phosphatase (ALP) activity was measured. The expression of osteoblast differentiation markers such as ALP, type-1 collagen (Col 1), and osteocalcin (OCN), and the expression of Id-1 and Id-2 were measured by RT-PCR. In order to understand the mechanism underlying the regulation of Id genes, the promoter region of the Id-1 gene was identified. Database analysis of the promoter region for Id-1 using known consensus sequences identified several putative response elements, including CCAAT/enhancer-binding protein beta (C/EBP beta). Alendronate treatment significantly increased not only ALP activity but also the expression of ALP, Col 1, and OCN, Id-1 and Id-2. C/EBP beta and alendronate cooperatively increased the promoter activity and expression of Id-1. These results suggest that C/EBP beta-mediated Id-1 transcriptional activation may regulate alendronate-induced osteoblast differentiation of C2C12 cells.
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