Promoting effect of 1,25(OH) 2 vitamin D 3 in osteogenic differentiation from induced pluripotent stem cells to osteocyte-like cells
Author(s) -
Hiroshi Kato,
Hiromi Ochiai-Shino,
Shoko Onodera,
Akiko Saito,
Takahiko Shibahara,
Toshifumi Azuma
Publication year - 2015
Publication title -
open biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.078
H-Index - 53
ISSN - 2046-2441
DOI - 10.1098/rsob.140201
Subject(s) - osteocyte , osteoblast , osteocalcin , runx2 , alkaline phosphatase , biology , induced pluripotent stem cell , microbiology and biotechnology , stem cell , medicine , cellular differentiation , endocrinology , embryonic stem cell , biochemistry , in vitro , gene , enzyme
We recently reported a new method to purify the induced pluripotent stem (iPS)-derived osteoprogenitors (iPSop). In this paper, we optimized the procedure and characterized cells at each process step. We observed that 10 days of treatment with FGF-2, IGF-1 and TGF-β (FIT) resulted in early-phase osteoblasts and 14 days of treatment resulted in late-phase osteoblasts. We found that treatment with 1,25(OH) 2 vitamin D 3 increased expression of osteocalcin and decreased expression of tissue-non-specific alkaline phosphatase and runt-related transcription factor 2 (RUNX2) in iPSop-day14 cells (cells treated with FIT for 14 days). Therefore, iPSop-day14 cells were promoted to mature osteoblasts by 1,25(OH) 2 vitamin D 3 treatment. In addition, we found that 1,25(OH) 2 vitamin D 3 treatment for 14 days enhanced not only mineralization but also expression of osteocyte markers, including dentin matrix protein-1 and fibroblast growth factor-23, in iPSop cells. Therefore, 1,25(OH) 2 vitamin D 3 is a potent promoter of osteoblast–osteocyte transition. The results of this study suggest that it is possible to evaluate both early- and late-phase osteoblasts and to apply cells to drug screening for anabolic drugs that stimulate bone formation.
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