Electrical stimulation promotes wound healing by enhancing dermal fibroblast activity and promoting myofibroblast transdifferentiation

• Published in: PloS one Vol. 8; no. 8; p. e71660
• Main Authors: Rouabhia, Mahmoud, Park, Hyunjin, Meng, Shiyun, Derbali, Habib, Zhang, Ze
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 19.08.2013; Public Library of Science (PLoS)
• Subjects: Actin; Actins - metabolism; Anticoagulants; Biology; Breast cancer; Cell adhesion & migration; Cell culture; Cell growth; Cell Proliferation; Cell Survival; Cell Transdifferentiation; Cells, Cultured; Collagen; Contraction; Cytotoxicity; Dentistry; Dermis - cytology; Dermis - physiology; Diabetes; Ecology; Electric fields; Electric properties; Electric Stimulation; Electrical stimuli; Engineering; Enzyme-Linked Immunosorbent Assay; Exposure; Extracellular matrix; Fibroblast growth factor 1; Fibroblast Growth Factor 1 - metabolism; Fibroblast growth factor 2; Fibroblast Growth Factor 2 - metabolism; Fibroblasts; Fibroblasts - cytology; Fibroblasts - metabolism; Genotype & phenotype; Growth factors; Heparin; Humans; Materials Science; Membranes; Microscopy, Fluorescence; Muscle contraction; Muscle, Smooth - chemistry; Muscles; Myofibroblasts - cytology; Myofibroblasts - metabolism; Physiology; Polylactic acid; Secretion; Skin; Smooth muscle; Stimulation; Surgery; Time Factors; Wound care; Wound Healing; Canada; Quebec City Quebec Canada
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0071660

Electrical stimulation (ES) has long been used as an alternative clinical treatment and an effective approach to modulate cellular behaviours. In this work we investigated the effects of ES on human skin fibroblast activity, myofibroblast transdifferentiation and the consequence on wound healing. Normal human fibroblasts were seeded on heparin-bioactivated PPy/PLLA conductive membranes, cultured for 24 h, and then exposed to ES of 50 or 200 mV/mm for 2, 4, or 6 h. Following ES, the cells were either subjected to various analyses or re-seeded to investigate their healing capacity. Our findings show that ES had no cytotoxic effect on the fibroblasts, as demonstrated by the similar LDH activity levels in the ES-exposed and non-exposed cultures, and by the comparable cell viability under both conditions. Furthermore, the number of viable fibroblasts was higher following exposure to 6 h of ES than in the non-exposed culture. This enhanced cell growth was likely due to the ES up-regulated secretion of FGF-1 and FGF-2. In an in vitro scratch-wound assay where cell monolayer was used as a healing model, the electrically stimulated dermal fibroblasts migrated faster following exposure to ES and recorded a high contractile behaviour toward the collagen gel matrix. This enhanced contraction was supported by the high level of α-smooth muscle actin expressed by the fibroblasts following exposure to ES, indicating the characteristics of myofibroblasts. Remarkably, the modulation of fibroblast growth continued long after ES. In conclusion, this work demonstrates for the first time that exposure to ES promoted skin fibroblast growth and migration, increased growth factor secretion, and promoted fibroblast to myofibroblast transdifferentiation, thus promoting wound healing.