Pulsed electromagnetic fields inhibit human osteoclast formation and gene expression via osteoblasts.

Author: He Z1, Selvamurugan N2, Warshaw J1, Partridge NC3
Affiliation:
1Department of Basic Biology and Craniofacial Biology, New York University College of Dentistry, New York, NY, USA.
2Department of Biotechnology, School of Bioengineering, SRM University, Kattankulathur, Tamil Nadu, India.
3Department of Basic Biology and Craniofacial Biology, New York University College of Dentistry, New York, NY, USA. Electronic address: ncp234@nyu.edu.
Conference/Journal: Bone.
Date published: 2017 Sep 28
Other: Pages: S8756-3282(17)30357-5 , Special Notes: doi: 10.1016/j.bone.2017.09.020. [Epub ahead of print] , Word Count: 190


Pulsed electromagnetic fields (PEMFs) can be effective in promoting the healing of delayed union or nonunion fractures. We previously reported that PEMF (Spinal-Stim® by Orthofix, Inc., Lewisville, TX) stimulated proliferation, differentiation and mineralization of rat calvarial osteoblastic cells in culture. In the present work we investigated the effects of PEMF (Physio-Stim® by Orthofix, Inc., Lewisville, TX) on human bone marrow macrophages (hBMMs) differentiated to osteoclasts. PEMF had striking inhibitory effects on formation of osteoclasts from hBMMs from both younger and older women. There were significantly greater changes in gene expression as ascertained by RNAseq from cells from older women. Interestingly, all of the genes identified by RNAseq were upregulated, and all were genes of mesenchymal or osteoblastic cells and included members of the TGF-β signaling pathway and many extracellular matrix proteins, as well as RANKL and osteoprotegerin, indicating the mixed nature of these cultures. From these results, we suggest that PEMF can inhibit osteoclast formation via action on osteoblasts. Thus, PEMF may be very effective for bone mass maintenance in subjects with osteoporosis.

Copyright © 2017. Published by Elsevier Inc.

KEYWORDS: Gene expression; Human osteoblasts; Human osteoclasts; PEMF

PMID: 28965919 DOI: 10.1016/j.bone.2017.09.020

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