Electromagnetic fields (EMF) have been shown to exert beneficial effects on cartilage tissue. Nowadays, differentiated human mesenchymal stem cells (hMSCs) are discussed as an alternative approach for cartilage repair. Therefore, the aim of this study was to examine the impact of EMF on hMSCs during
Pulsed electromagnetic fields enhance BMP-2 dependent osteoblastic differentiation of human mesenchymal stem cells
โ Scribed by Z. Schwartz; B. J. Simon; M. A. Duran; G. Barabino; R. Chaudhri; B. D. Boyan
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 266 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0736-0266
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Mesenchymal stem cells (MSCs) express an osteoblastic phenotype when treated with BMPโ2, and BMPโ2 is used clinically to induce bone formation although high doses are required. Pulsed electromagnetic fields (PEMF) also promote osteogenesis in vivo, in part through direct action on osteoblasts. We tested the hypothesis that PEMF enhances osteogenesis of MSCs in the presence of an inductive stimulus like BMPโ2. Confluent cultures of human MSCs were grown on calcium phosphate disks and were treated with osteogenic media (OM), OM containing 40 ng/mL rhBMPโ2, OMโ+โPEMF (8 h/day), or OMโ+โBMPโ2โ+โPEMF. MSCs demonstrated minor increases in alkaline phosphatase (ALP) during 24 days in culture and no change in osteocalcin. OM increased ALP and osteocalcin by day 6, but PEMF had no additional effect at any time. BMPโ2 was stimulatory over OM, and PEMFโ+โBMPโ2 synergistically increased ALP and osteocalcin. PEMF also enhanced the effects of BMPโ2 on PGE2, latent and active TGFโฮฒ1, and osteoprotegerin. Effects of PEMF on BMPโ2โtreated cells were greatest at days 12 to 20. These results demonstrate that PEMF enhances osteogenic effects of BMPโ2 on MSCs cultured on calcium phosphate substrates, suggesting that PEMF will improve MSC response to BMPโ2 in vivo in a bone environment. ยฉ 2008 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 26:1250โ1255, 2008
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