z-logo
Premium
Pulsed electromagnetic fields enhance BMP‐2 dependent osteoblastic differentiation of human mesenchymal stem cells
Author(s) -
Schwartz Z.,
Simon B. J.,
Duran M. A.,
Barabino G.,
Chaudhri R.,
Boyan B. D.
Publication year - 2008
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.20591
Subject(s) - mesenchymal stem cell , osteocalcin , alkaline phosphatase , chemistry , bone morphogenetic protein 2 , in vivo , osteoprotegerin , calcium , in vitro , microbiology and biotechnology , endocrinology , biology , biochemistry , enzyme , activator (genetics) , organic chemistry , gene
Mesenchymal stem cells (MSCs) express an osteoblastic phenotype when treated with BMP‐2, and BMP‐2 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 BMP‐2. Confluent cultures of human MSCs were grown on calcium phosphate disks and were treated with osteogenic media (OM), OM containing 40 ng/mL rhBMP‐2, OM + PEMF (8 h/day), or OM + BMP‐2 + PEMF. 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. BMP‐2 was stimulatory over OM, and PEMF + BMP‐2 synergistically increased ALP and osteocalcin. PEMF also enhanced the effects of BMP‐2 on PGE2, latent and active TGF‐β1, and osteoprotegerin. Effects of PEMF on BMP‐2–treated cells were greatest at days 12 to 20. These results demonstrate that PEMF enhances osteogenic effects of BMP‐2 on MSCs cultured on calcium phosphate substrates, suggesting that PEMF will improve MSC response to BMP‐2 in vivo in a bone environment. © 2008 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 26:1250–1255, 2008

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here