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Blue Light (λ = 453 nm) Significantly Reduces TGF-β-Induced Fibroblast Differentiation Through Reversible Disruption
Pia Steentjes1, Julia Krassovka1, Christoph V Suschek1
1Department for Orthopedics and Trauma Surgery, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, Moorenstr. 5, 40225 Düsseldorf, Germany.
Abstract:
Background/Objectives: Abnormal differentiation of human skin fibroblasts into myofibroblasts contributes to fibrotic skin disorders such as hypertrophic scars, keloids, and Dupuytren's disease. This process is characterized by increased fibroblast proliferation, enhanced differentiation into myofibroblasts, and reduced programmed cell death (apoptosis). We previously demonstrated that blue light irradiation (λ = 453 nm) significantly and dose-dependently inhibits both spontaneous and TGF-β-induced fibroblast differentiation. Methods: Because fibroblast differentiation depends on cellular energy metabolism, we investigated whether the inhibitory effect of blue light is linked to changes in the cells' energy balance. Results: We found that blue light reduced TGF-β-induced differentiation, as shown by decreased levels of α-SMA and EDA-fibronectin, key markers of myofibroblast formation. This effect was strongly associated with almost complete inhibition of mitochondrial respiration, reduced glycolysis, a lower NAD+/NADH ratio, and decreased ATP production. ATP-dependent processes, including endocytosis and lysosomal activity, both essential parameters of fibroblast differentiation, were also strongly suppressed. Importantly, all these changes were fully reversible within 24 h after the last irradiation. Conclusions: Mechanistically, we propose that blue light triggers photochemical reduction in flavins in proteins of the respiratory chain and possibly the Krebs cycle, which temporarily alters cellular energy metabolism. These findings suggest that non-toxic blue light therapy (80 J/cm2) can effectively prevent factor-induced fibroblast differentiation and may serve as a standalone or supportive treatment to reduce fibrotic events such as scarring and keloid formation. Furthermore, our results indicate that targeting cellular energy metabolism, whether physically or pharmacologically, could be a promising strategy to prevent sclerotic skin disorders.
Insights
Blue light therapy inhibits fibroblast differentiation into myofibroblasts, a key process in fibrotic skin disorders. This effect is linked to temporary changes in cellular energy metabolism, offering a potential treatment for scarring and keloids.
Area of Science:
- Dermatology
- Cell Biology
- Biochemistry
Background:
- Abnormal fibroblast differentiation into myofibroblasts drives fibrotic skin disorders like hypertrophic scars and keloids.
- This process involves increased proliferation, differentiation, and reduced apoptosis of fibroblasts.
- Previous studies showed blue light irradiation inhibits fibroblast differentiation.
Purpose of the Study:
- Investigate if blue light's inhibitory effect on fibroblast differentiation is linked to cellular energy metabolism.
- Elucidate the mechanism by which blue light impacts fibroblast energy balance.
Main Methods:
- Exposed human skin fibroblasts to blue light (453 nm).
- Assessed myofibroblast differentiation markers (α-SMA, EDA-fibronectin).
- Measured cellular energy metabolism parameters: mitochondrial respiration, glycolysis, NAD+/NADH ratio, ATP production, and ATP-dependent processes.
Main Results:
- Blue light significantly reduced TGF-β-induced fibroblast differentiation markers.
- This was associated with inhibited mitochondrial respiration, glycolysis, NAD+/NADH ratio, and ATP production.
- ATP-dependent processes like endocytosis and lysosomal activity were suppressed; all effects were reversible within 24 hours.
Conclusions:
- Blue light therapy temporarily alters cellular energy metabolism by affecting flavins in the respiratory chain and Krebs cycle.
- Non-toxic blue light (80 J/cm²) can prevent factor-induced fibroblast differentiation, suggesting potential for treating fibrotic skin conditions.
- Targeting cellular energy metabolism presents a promising strategy for preventing and treating sclerotic skin disorders.
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