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Up‐regulation of expression of selected genes in human bone cells with specific capacitively coupled electric fields
Author(s) -
Clark Charles C.,
Wang Wei,
Brighton Carl T.
Publication year - 2014
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.22595
Subject(s) - osteocalcin , duty cycle , context (archaeology) , bone healing , transforming growth factor , bone morphogenetic protein , stimulation , alkaline phosphatase , chemistry , materials science , microbiology and biotechnology , biology , gene , endocrinology , anatomy , electrical engineering , biochemistry , enzyme , engineering , voltage , paleontology
The objective of the described experiments was to determine the electrical parameters that lead to optimal expression of a number of bone‐related genes in cultured human bone cells exposed to a capacitively coupled electric field. Human calvarial osteoblasts were grown in modified plastic Cooper dishes in which the cells could be exposed to various capacitively coupled electric fields. The optimal duration of stimulation and optimal duration of response to the electrical field, and the optimal amplitude, frequency and duty cycle were all determined for each of the genes analyzed. Results indicated that a capacitively coupled electric field of 60 kHz, 20 mV/cm, 50% duty cycle for 2 h duration per day significantly up‐regulated mRNA expression of a number of transforming growth factor (TGF)‐β family genes (bone morphogenetic proteins (BMP)‐2 and ‐4, TGF‐β1, ‐ β2 and ‐β3) as well as fibroblast growth factor (FGF)‐2, osteocalcin (BGP) and alkaline phosphatase (ALP). Protein levels of BMP‐2 and ‐4, and TGF‐β1 and ‐ β2 were also elevated. The clinical relevance of these findings in the context of a noninvasive treatment modality for delayed union and nonunion fracture healing is discussed. © 2014 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:894–903, 2014.
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