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Photobiomodulation at 660 nm Stimulates Fibroblast Differentiation
Author(s) -
Mokoena Dimakatso R.,
Houreld Nicolette N.,
Dhilip Kumar Sathish S.,
Abrahamse Heidi
Publication year - 2020
Publication title -
lasers in surgery and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.888
H-Index - 112
eISSN - 1096-9101
pISSN - 0196-8092
DOI - 10.1002/lsm.23204
Subject(s) - myofibroblast , fibroblast , fibronectin , wound healing , viability assay , transforming growth factor , fibrosis , diabetic foot , extracellular matrix , medicine , cancer research , receptor , microbiology and biotechnology , cell , andrology , chemistry , pathology , biology , immunology , endocrinology , diabetes mellitus , in vitro , biochemistry
Background and Objectives Among many of the different complications that diabetic patients suffer, foot ulcers are the most challenging, and in many cases result in non‐traumatic lower limb amputation and permanent disability. To alleviate this burden, new interventions such as photobiomodulation (PBM) have been utilized. However, the cellular pathways affected by PBM have not yet been fully recognized. The differentiation of fibroblasts into myofibroblasts forms a vital part of wound healing and is often impaired under diabetic conditions. Therefore, this study sought to investigate the effects of PBM at 660 nm on the transforming growth factor‐β1 (TGF‐β1)/Smad pathway and the differentiation of fibroblasts into myofibroblasts. Study Design/Materials and Methods WS1 fibroblasts were treated with PBM using a wavelength of 660 nm at a fluence of 5 J/cm 2 in normal, normal wounded, diabetic, and diabetic wounded models. Post‐irradiation cellular responses were observed at 24, 48, and 72 hours to ascertain morphological changes and cell viability, and the expression of fibroblast differentiation markers (Thy‐1 or CD90, extra domain A fibronectin or EDA‐FN and α‐smooth muscle actin or α‐SMA), TGF‐β1, phosphorylated (p)TGF‐β receptor 1 (R1), and p‐Smad2/3. Results There was a significant increase in cell viability in all irradiated cell models, and no real significant changes in TGF‐β1, pTGF‐β1R1, and p‐Smad2/3. As incubation time post‐irradiation increased, Thy‐1 (CD90) decreased, while EDA‐FN and α‐SMA increased in wounded models. Conclusions PBM at 660 nm with 5 J/cm 2 was successful in stimulating the differentiation of fibroblasts into myofibroblasts in diabetic wounded cells, which was independent of the TGF‐β1/Smad pathway. Fibroblast transition into myofibroblasts is vital to wound healing, failure of which results in impaired healing; PBM is able to foster such a transition. Lasers Surg. Med. © 2019 Wiley Periodicals, Inc.