Low-Level Light Therapy with 410 nm Light Emitting Diode Suppresses Collagen Synthesis in Human Keloid Fibroblasts: An In Vitro Study
2
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Background: Keloids are characterized by excessive collagen deposition in the dermis, in which transforming growth factor β (TGF-β)/Smad signaling plays an important role. Low-level light therapy (LLLT) is reported as effective in preventing keloids in clinical reports, recently. To date, studies investigating the effect of LLLT on keloid fibroblasts are extremely rare. Objective: We investigated the effect of LLLT with blue (410 nm), red (630 nm), and infrared (830 nm) light on the collagen synthesis in keloid fibroblasts. Methods: Keloid fibroblasts were isolated from keloid-revision surgery samples and irradiated using 410-, 630-, 830-nm light emitting diode twice, with a 24-hour interval at 10 J/cm2. After irradiation, cells were incubated for 24 and 48 hours and real- time quantitative reverse transcription polymerase chain reaction was performed. Western blot analysis was also performed in 48 hours after last irradiation. The genes and proteins of collagen type I, TGF-β1, Smad3, and Smad7 were analyzed. Results: We observed no statistically significant change in the viability of keloid fibroblasts after irradiation. Collagen type I was the only gene whose expression significantly decreased after irradiation at 410 nm when compared to the non-irradiated control. Western blot analysis showed that LLLT at 410 nm lowered the protein levels of collagen type I compared to the control. Conclusion: LLLT at 410 nm decreased the expression of collagen type I in keloid fibroblasts and might be effective in preventing keloid formation in their initial stage.
Abstract
Background: Keloids are characterized by excessive collagen deposition in the dermis, in which transforming growth factor β (TGF-β)/Smad signaling plays an important role. Low-level light therapy (LLLT) is reported as effective in preventing keloids in clinical reports, recently. To date, studies investigating the effect of LLLT on keloid fibroblasts are extremely rare. Objective: We investigated the effect of LLLT with blue (410 nm), red (630 nm), and infrared (830 nm) light on the collagen synthesis in keloid fibroblasts. Methods: Keloid fibroblasts were isolated from keloid-revision surgery samples and irradiated using 410-, 630-, 830-nm light emitting diode twice, with a 24-hour interval at 10 J/cm2. After irradiation, cells were incubated for 24 and 48 hours and real- time quantitative reverse transcription polymerase chain reaction was performed. Western blot analysis was also performed in 48 hours after last irradiation. The genes and proteins of collagen type I, TGF-β1, Smad3, and Smad7 were analyzed. Results: We observed no statistically significant change in the viability of keloid fibroblasts after irradiation. Collagen type I was the only gene whose expression significantly decreased after irradiation at 410 nm when compared to the non-irradiated control. Western blot analysis showed that LLLT at 410 nm lowered the protein levels of collagen type I compared to the control. Conclusion: LLLT at 410 nm decreased the expression of collagen type I in keloid fibroblasts and might be effective in preventing keloid formation in their initial stage.
참고문헌 (23)
- Tsujita-Kyutoku M, "Comparison of transforming growth factor-beta", Smad signaling between normal dermal fibroblasts and fibroblasts derived from central and peripheral areas of keloid lesions, 2005, pp.19, 959~963
- 박선이, "Effects of Xanthium stramarium and Psoralea corylifolia Extracts Combined with UVA1 Irradiation on the Cell Proliferation and TGF-β1 Expression of Keloid Fibroblasts", Annals of Dermatology, 25(3), pp.304~309 (2013), 대한피부과학회
- Chin GS, "Differential expression of transforming growth factorbeta receptors I and II and activation of Smad 3 in keloid fibroblasts", Plast Reconstr Surg, 108, pp.423~429 (2001)
- Jagadeesan J, "Transforming growth factor beta (TGFbeta) and keloid disease", Int J Surg, 5, pp.278~285 (2007)
- Phan TT, "Smad3 signalling plays an important role in keloid pathogenesis via epithelial-mesenchymal interactions", J Pathol, 207, pp.232~242 (2005)
- Mamalis AD, "Laser and light-based treatment of Keloids--a review", J Eur Acad Dermatol Venereol, 28, pp.689~699 (2014)
- Barolet D, "Prophylactic low-level light therapy for the treatment of hypertrophic scars and keloids: a case series", Lasers Surg Med, 42, pp.597~601 (2010)
- Carvalho RL, "Effects of low-level laser therapy on pain and scar formation after inguinal herniation surgery: a randomized controlled single-blind study", Photomed Laser Surg, 28, pp.417~422 (2010)
- da Silva JP, "Laser therapy in the tissue repair process: a literature review", Photomed Laser Surg, 28, pp.17~21 (2010)
- Hamblin MR, "Mechanisms of low level light therapy", Proc of SPIE, 6140, pp.614001~6140012 (2006)
- Mamalis A, "Light emitting diodegenerated blue light modulates fibrosis characteristics:fibroblast proliferation, migration speed, and reactive oxygen species generation", Lasers Surg Med, 47, pp.210~215 (2015)
- Gorgidze LA, "Blue light inhibits mitosis in tissue culture cells", Biosci Rep, 18, pp.215~224 (1998)
- Eichler M, "Flavins are source of visible-light-induced free radical formation in cells", Lasers Surg Med, 37, pp.314~319 (2005)
- Opländer C, "Effects of blue light irradiation on human dermal fibroblasts", J Photochem Photobiol B, 103, pp.118~125 (2011)
- Bonatti S, "In vitro effect of 470 nm LED (Light Emitting Diode) in keloid fibroblasts", Acta Cir Bras, 26, pp.25~30 (2011)
- Seo YK, "Comparison of light-emitting diode wavelength on activity and migration of rabbit ACL cells", Lasers Med Sci, 29, pp.245~255 (2014)
- He S, "Mechanisms of transforming growth factor beta(1)", Smad signalling mediated by mitogen-activated protein kinase pathways in keloid fibroblasts, 2010, pp.162, 538~546
- Lim IJ, "Synchronous activation of ERK and phosphatidylinositol 3-kinase pathways is required for collagen and extracellular matrix production in keloids", J Biol Chem, 278, pp.40851~40858 (2003)
- Kuo YR, "Activation of ERK and p38 kinase mediated keloid fibroblast apoptosis after flashlamp pulsed-dye laser treatment", Lasers Surg Med, 36, pp.31~37 (2005)
- Kuo YR, "Flashlamp pulsed-dye laser suppressed TGF-beta1 expression and proliferation in cultured keloid fibroblasts is mediated by MAPK pathway", Lasers Surg Med, 39, pp.358~364 (2007)
- Igota S, "Identification and characterization of Wnt signaling pathway in keloid pathogenesis", Int J Med Sci, 10, pp.344~354 (2013)
- Babu M, "Keloid fibroblasts exhibit an altered response to TGF-beta", J Invest Dermatol, 99, pp.650~655 (1992)
- Younai S, "Modulation of collagen synthesis by transforming growth factor-beta in keloid and hypertrophic scar fibroblasts", Ann Plast Surg, 33, pp.148~151 (1994)
