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Published on: November 16, 2018
MicroRNA expression analysis of human skin fibroblasts treated with high-fluence light-emitting diode-red light
Andrew Mamalis1,2, Eugene Koo2,3, Clifford Tepper4
1Department of Dermatology, SUNY Downstate Medical Center, Brooklyn, New York.
Abstract:
Skin fibrosis is a chronic debilitating feature of several skin diseases that lead to characteristic increases in dermal fibroblast proliferation and collagen deposition through upregulation in components of the transforming growth factor beta (TGF-B)/SMAD pathway. In contrast to ultraviolet phototherapy, high-fluence light-emitting diode-generated red light (HF-LED-RL, 633 ± 15 nm) is a safe, economic and non-invasive therapy with in vitro evidence that supports modulation of the key cellular characteristics involved in the pathogenesis of skin fibrosis. Limited data exists pertaining to the effects of HF-LED-RL on human skin fibroblast microRNA (miRNA). Herein, we explored the effects of HF-LED-RL on fibroblast miRNA levels using RNA-seq and miRNA expression analysis. Using RNA-seq analysis we found that HF-LED-RL at 320 and 640 J/cm2 increased transcription of key miRNA that are involved in skin fibrosis including miRNA-29, miRNA-196a and Let-7a, and decreased transcription of miRNA-21, miRNA-23b and miRNA-31. These microRNA findings provide insight into the molecular underpinnings of HF-LED-RL and highlight potential therapeutic targets of interest for the treatment of skin fibrosis. Additional research on the specific molecular mechanisms underlying HF-LED-RL effects on fibroblasts may provide further mechanistic insight into this therapy and may reveal additional future therapeutic targets for skin fibrosis.
Insights
High-fluence red light therapy (HF-LED-RL) safely modulates microRNA (miRNA) in skin fibroblasts. This safe, non-invasive treatment shows promise for targeting molecular pathways involved in skin fibrosis.
Area of Science:
- Dermatology and Molecular Biology
- Investigating the molecular mechanisms of skin fibrosis and novel therapeutic interventions.
Background:
- Skin fibrosis, characterized by fibroblast proliferation and collagen deposition, is driven by the transforming growth factor beta (TGF-B)/SMAD pathway.
- High-fluence light-emitting diode-generated red light (HF-LED-RL) is a safe, non-invasive therapy with potential to modulate fibrotic processes.
- Limited research exists on HF-LED-RL's effects on human skin fibroblast microRNAs (miRNAs).
Purpose of the Study:
- To explore the impact of HF-LED-RL on miRNA expression in human skin fibroblasts.
- To identify specific miRNAs modulated by HF-LED-RL that are relevant to skin fibrosis pathogenesis.
Main Methods:
- Utilized RNA sequencing (RNA-seq) and miRNA expression analysis.
- Exposed human skin fibroblasts to HF-LED-RL at energy densities of 320 J/cm² and 640 J/cm².
- Analyzed changes in miRNA transcription levels post-treatment.
Main Results:
- HF-LED-RL significantly altered the transcription of several key miRNAs involved in skin fibrosis.
- Increased transcription of fibrosis-associated miRNAs: miRNA-29, miRNA-196a, and Let-7a.
- Decreased transcription of fibrosis-associated miRNAs: miRNA-21, miRNA-23b, and miRNA-31.
Conclusions:
- The observed miRNA modulations provide insight into the molecular mechanisms of HF-LED-RL in treating skin fibrosis.
- Specific miRNAs identified represent potential therapeutic targets for skin fibrosis.
- Further research into the precise molecular mechanisms of HF-LED-RL is warranted to uncover additional therapeutic targets.
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