Electrical stimulation promotes the proliferation of human keratinocytes, increases the production of keratin 5 and 14, and increases the phosphorylation of ERK1/2 and p38 MAP kinases

伤口愈合 p38丝裂原活化蛋白激酶 角质形成细胞 细胞生物学 角蛋白 磷酸化 激酶 刺激 丝裂原活化蛋白激酶 细胞生长 化学 生物 免疫学 MAPK/ERK通路 医学 内分泌学 病理 生物化学 体外
作者
Mahmoud Rouabhia,Hyun Jin Park,Atieh Abedin‐Do,Yvan Douville,Mireille Méthot,Ze Zhang
出处
期刊:Journal of Tissue Engineering and Regenerative Medicine [Wiley]
卷期号:14 (7): 909-919 被引量:40
标识
DOI:10.1002/term.3040
摘要

Effective wound healing remains a significant clinical challenge in reducing patient morbidity and improving quality of life. Wound healing is a complex process involving the endogenous electrical field. The electrical field can contribute to wound healing by activating keratinocytes to promote reepithelialization. The objective of this study was to determine the effects of exogenous electrical stimulation (ES) on human keratinocyte viability and proliferation and on production of IL-6, IL-8, and keratins (K5 and K14) and to investigate the activated signalling pathways in keratinocytes exposed to ES. Keratinocytes were cultured under ES at different intensities for 6 or 24 hr. Cell proliferation, cytokines and growth factors, K5 and K14, as well as phosphorylated ERK1/2 and p38 MAP kinases, were evaluated. The results showed that the keratinocytes exposed to ES between 100 and 150 mV/mm for 6 or 24 hr showed a significantly increased proliferation rate. However, a 24 hr exposure to 200 mV/mm revealed no significant effect in cell growth. ES at 100 and 200 mV/mm for 6 hr increased the secretion of epidermal growth factor and vascular endothelial growth factor, and the production of K5 and K14. K14 was more sensitive than K5 to ES. However, ES down-regulated the secretions of IL-6 and IL-8. Finally, ES increased the phosphorylation of ERK1/2 and p38 MAP kinases. Overall results suggested that ES can be useful in supporting skin wound healing by activating keratinocytes.
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