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Photobiomodulation at 660 nm Stimulates Fibroblast Differentiation

Mokoena DR, Houreld NN, Dhilip Kumar SS, Abrahamse H

Lasers in surgery and medicine · 41 citas

Etiquetas de revisión

Solo mecanismos

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Cómo se estudió

Diseño
Estudio in vitro o de mecanismos (clasificado por nuestro filtro de IA)
Estudiado en
Células o muestras de laboratorio
Resultado principal
Solo mecanismos

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Research Foundation
Universidad u hospital
University of Johannesburg
Subvenciones
National Research Foundation (112114); University of Johannesburg (020930)

Según 2 financiadores declarados.

Publicación

Publicado
2019-12-09 · Lasers Surg Med · vol. 52 · número 7 · págs. 671–681
Editorial
Wiley
Citado
51 citas · más que el 93% de estudios similares · 3.6× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
37 trabajos
Acceso
De pago
Áreas de investigación
Laser Applications in Dentistry and Medicine · Wound Healing and Treatments · Medical and Biological Ozone Research
Palabras clave
Fibroblast, Chemistry, Cell biology, Biology, Biochemistry, In vitro
MeSH
cells, cultured, fibroblasts, humans, wound healing, cell differentiation, cell survival, myofibroblasts

4 autores

  • Dimakatso R. Mokoena🇿🇦University of Johannesburg
  • Nicolette N. Houreld🇿🇦 · autor de correspondenciaUniversity of Johannesburg
  • Sathish Sundar Dhilip Kumar🇿🇦University of Johannesburg
  • Heidi Abrahamse🇿🇦University of Johannesburg

Resumen

El texto original del estudio, en el idioma en que se publicó.

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/cm2 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/cm2 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.

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