Study2020

Photobiomodulation at 660 nm Stimulates Fibroblast Differentiation

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

Lasers in surgery and medicine · 41 citations

Review labels

Mechanisms only

Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.

How it was studied

Design
In vitro/mechanistic study (classified by our AI screen)
Studied in
Cells or lab samples
Main outcome
Mechanisms only

Who paid for it

Funding
Independent funding
Government
National Research Foundation
University or hospital
University of Johannesburg
Grants
National Research Foundation (112114); University of Johannesburg (020930)

Based on 2 listed funder(s).

Publication

Published
2019-12-09 · Lasers Surg Med · vol. 52 · issue 7 · pp. 671–681
Publisher
Wiley
Cited
51 citations · more than 93% of similar papers · 3.6× the field average
Impact
Top 10% most cited in its field
References
37 works
Access
Paywalled
Research areas
Laser Applications in Dentistry and Medicine · Wound Healing and Treatments · Medical and Biological Ozone Research
Keywords
Fibroblast, Chemistry, Cell biology, Biology, Biochemistry, In vitro
MeSH
cells, cultured, fibroblasts, humans, wound healing, cell differentiation, cell survival, myofibroblasts

4 authors

From ZA

  • Dimakatso R. MokoenaUniversity of Johannesburg
  • Nicolette N. Houreld · correspondingUniversity of Johannesburg
  • Sathish Sundar Dhilip KumarUniversity of Johannesburg
  • Heidi AbrahamseUniversity of Johannesburg

Abstract

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.

Abstract via Europe PMC. Copyright remains with the authors or publisher.

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