4.7 Article

Regulation of osteogenic differentiation of human adipose-derived stem cells by controlling electromagnetic field conditions

Journal

EXPERIMENTAL AND MOLECULAR MEDICINE
Volume 45, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/emm.2013.11

Keywords

adipose-derived stem cells; electromagnetic field; frequency; magnetic flux density; optimization; osteogenic differentiation

Funding

  1. National Research Foundation of Korea (NRF)
  2. Korea government (MEST) [2012-0001235]
  3. World Class University (WCU) program through the National Research Foundation of Korea
  4. Ministry of Education, Science and Technology [R31-2008-000-10105-0]

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Many studies have reported that an electromagnetic field can promote osteogenic differentiation of mesenchymal stem cells. However, experimental results have differed depending on the experimental and environmental conditions. Optimization of electromagnetic field conditions in a single, identified system can compensate for these differences. Here we demonstrated that specific electromagnetic field conditions (that is, frequency and magnetic flux density) significantly regulate osteogenic differentiation of adipose-derived stem cells (ASCs) in vitro. Before inducing osteogenic differentiation, we determined ASC stemness and confirmed that the electromagnetic field was uniform at the solenoid coil center. Then, we selected positive (30/45 Hz, 1 mT) and negative (7.5 Hz, 1 mT) osteogenic differentiation conditions by quantifying alkaline phosphate (ALP) mRNA expression. Osteogenic marker (for example, runt-related transcription factor 2) expression was higher in the 30/45 Hz condition and lower in the 7.5 Hz condition as compared with the nonstimulated group. Both positive and negative regulation of ALP activity and mineralized nodule formation supported these responses. Our data indicate that the effects of the electromagnetic fields on osteogenic differentiation differ depending on the electromagnetic field conditions. This study provides a framework for future work on controlling stem cell differentiation. Experimental & Molecular Medicine (2013) 45, e6; doi:10.1038/emm.2013.11;published online 25 January 2013

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