4.0 Article

Functions of vitamin D, retinoic acid, and dexamethasone in mouse adipose-derived mesenchymal cells

Journal

TISSUE ENGINEERING
Volume 12, Issue 7, Pages 2031-2040

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ten.2006.12.2031

Keywords

-

Funding

  1. NIDCR NIH HHS [R01 DE-14526, R01 DE-13194] Funding Source: Medline
  2. NIGMS NIH HHS [K08 GM069677] Funding Source: Medline

Ask authors/readers for more resources

Adipose-derived mesenchymal cells (AMCs) offer great promise for tissue engineering of bone. Previously, 1,25-dihydroxyvitamin D3, retinoic acid (RA), and dexamethasone had been shown to promote osteogenesis in bone marrow-derived mesenchymal cells (BMSCs). To study the osteogenic characteristics of mouse AMCs, we applied these 3 hormones alone and in combination to the AMCs and examined markers of osteogenic differentiation. Interestingly, vitamin D and RA demonstrated a consistent, dose-dependent enhancement of osteogenesis and upregulated osteoblast specific markers including osteopontin and osteocalcin. However, in AMCs, dexamethasone clearly inhibited osteogenic differentiation in a dose-dependent fashion and greatly increased the adipogenic marker peroxisome proliferator activated receptor gamma (PPARc). In summary, we show in vitro that vitamin D and RA are potential candidates to serve as enhancers of osteogenesis of AMCs and may be incorporated into future cell-based strategies for bone tissue engineering.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available