| Literature DB >> 31736106 |
Juan Felipe Escobar1,2, Juan Jairo Vaca-González1,3, Johana Maria Guevara4, Jose Félix Vega5, Yoshie Adriana Hata1,2, Diego Alexander Garzón-Alvarado1,2.
Abstract
Magnetic fields (MFs) have been used as an external stimulus to increase cell proliferation in chondrocytes and extracellular matrix (ECM) synthesis of articular cartilage. However, previously published studies have not shown that MFs are homogeneous through cell culture systems. In addition, variables such as stimulation times and MF intensities have not been standardized to obtain the best cellular proliferative rate or an increase in molecular synthesis of ECM. In this work, a stimulation device, which produces homogeneous MFs to stimulate cell culture surfaces was designed and manufactured using a computational model. Furthermore, an in vitro culture of primary rat chondrocytes was established and stimulated with two MF schemes to measure both proliferation and ECM synthesis. The best proliferation rate was obtained with an MF of 2 mT applied for 3 h, every 6 h for 8 days. In addition, the increase in the synthesis of glycosaminoglycans was statistically significant when cells were stimulated with an MF of 2 mT applied for 5 h, every 6 h for 8 days. These findings suggest that a stimulation with MFs is a promising tool that could be used to improve in vitro treatments such as autologous chondrocyte implantation, either to increase cell proliferation or stimulate molecular synthesis. Bioelectromagnetics. 2020;41:41-51Entities:
Keywords: articular cartilage; cell proliferation; chondrocyte; glycosaminoglycans; magnetic fields
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Year: 2019 PMID: 31736106 DOI: 10.1002/bem.22231
Source DB: PubMed Journal: Bioelectromagnetics ISSN: 0197-8462 Impact factor: 2.010