Weak Electromagnetic Fields Accelerate Fusion of Myoblasts.Show others and affiliations
2021 (English)In: International Journal of Molecular Sciences, ISSN 1661-6596, E-ISSN 1422-0067, Vol. 22, no 9, article id 4407
Article in journal (Refereed) Published
Abstract [en]
Weak electromagnetic fields (WEF) alter Ca2+ handling in skeletal muscle myotubes. Owing to the involvement of Ca2+ in muscle development, we investigated whether WEF affects fusion of myoblasts in culture. Rat primary myoblast cultures were exposed to WEF (1.75 µT, 16 Hz) for up to six days. Under control conditions, cell fusion and creatine kinase (CK) activity increased in parallel and peaked at 4-6 days. WEF enhanced the extent of fusion after one and two days (by ~40%) vs. control, but not thereafter. Exposure to WEF also enhanced CK activity after two days (almost four-fold), but not afterwards. Incorporation of 3H-thymidine into DNA was enhanced by one-day exposure to WEF (~40%), indicating increased cell replication. Using the potentiometric fluorescent dye di-8-ANEPPS, we found that exposure of cells to 150 mM KCl resulted in depolarization of the cell membrane. However, prior exposure of cells to WEF for one day followed by addition of KCl resulted in hyperpolarization of the cell membrane. Acute exposure of cells to WEF also resulted in hyperpolarization of the cell membrane. Twenty-four hour incubation of myoblasts with gambogic acid, an inhibitor of the inward rectifying K+ channel 2.1 (Kir2.1), did not affect cell fusion, WEF-mediated acceleration of fusion or hyperpolarization. These data demonstrate that WEF accelerates fusion of myoblasts, resulting in myotube formation. The WEF effect is associated with hyperpolarization but WEF does not appear to mediate its effects on fusion by activating Kir2.1 channels.
Place, publisher, year, edition, pages
MDPI, 2021. Vol. 22, no 9, article id 4407
Keywords [en]
creatine kinase, differentiation, fusion, myoblasts, myotubes, weak electromagnetic fields
National Category
Endocrinology and Diabetes
Research subject
Medicine/Technology
Identifiers
URN: urn:nbn:se:gih:diva-6692DOI: 10.3390/ijms22094407ISI: 000650349500001PubMedID: 33922487OAI: oai:DiVA.org:gih-6692DiVA, id: diva2:1555495
2021-05-182021-05-182022-02-10