Matches in SemOpenAlex for { <https://semopenalex.org/work/W2103240590> ?p ?o ?g. }
- W2103240590 endingPage "215" @default.
- W2103240590 startingPage "210" @default.
- W2103240590 abstract "Background and Objective Blue light is part of the visible light spectrum that does not generate harmful DNA adducts associated with skin cancer and photoaging, and may represent a safer therapeutic modality for treatment of keloid scars and other fibrotic skin diseases. Our laboratory previously demonstrated that light-emitting diode (LED) red and infrared light inhibits proliferation of skin fibroblasts. Moreover, different wavelengths of light can produce different biological effects. Furthermore, the effects of LED blue light (LED-BL) on human skin fibroblasts are not well characterized. This study investigated the effects of LED-BL on human skin fibroblast proliferation, viability, migration speed, and reactive oxygen-species (ROS) generation. Methods and Materials Irradiation of adult human skin fibroblasts using commercially-available LED-BL panels was performed in vitro, and modulation of proliferation and viability was quantified using the trypan blue dye exclusion assay, migratory speed was assessed using time-lapse video microscopy, and intracellular ROS generation was measured using the dihydrorhodamine flow cytometry assay. Statistical differences between groups were determined by ANOVA and Student's t-test. Results Human skin fibroblasts treated with LED-BL fluences of 5, 10, 15, 30, and 80 J/cm2 demonstrated statistically significant dose-dependent decreases in relative proliferation of 8.4%, 29.1%, 33.8%, 51.7%, and 55.1%, respectively, compared to temperature and environment matched bench control plates, respectively. LED-BL fluences of 5, 30, 45, and 80 J/cm2 decreased fibroblast migration speed to 95 ± 7.0% (P = 0.64), 81.3 ± 5.5% (P = 0.021), 48.5 ± 2.7% (P < 0.0001), and 32.3 ± 1.9% (P < 0.0001), respectively, relative to matched controls. LED fluences of 5, 10, 30, and 80 J/cm2 resulted in statistically significant increases in reactive oxygen species of 110.4%, 116.6%, 127.5%, and 130%, respectively, relative to bench controls. Conclusion At the fluences studied, LED-BL can inhibit adult human skin dermal fibroblast proliferation and migration speed, and is associated with increased reactive oxygen species generation in a dose-dependent manner without altering viability. LED-BL has the potential to contribute to the treatment of keloids and other fibrotic skin diseases and is worthy of further translational and clinical investigation. Lasers Surg. Med. 47:210–215, 2015. © 2015 Wiley Periodicals, Inc." @default.
- W2103240590 created "2016-06-24" @default.
- W2103240590 creator A5012429566 @default.
- W2103240590 creator A5014431093 @default.
- W2103240590 creator A5085162752 @default.
- W2103240590 date "2015-02-01" @default.
- W2103240590 modified "2023-10-12" @default.
- W2103240590 title "Light emitting diode-generated blue light modulates fibrosis characteristics: Fibroblast proliferation, migration speed, and reactive oxygen species generation" @default.
- W2103240590 cites W1670324689 @default.
- W2103240590 cites W194850094 @default.
- W2103240590 cites W1966839121 @default.
- W2103240590 cites W1974847687 @default.
- W2103240590 cites W1980995375 @default.
- W2103240590 cites W1984382407 @default.
- W2103240590 cites W1993118852 @default.
- W2103240590 cites W1997925504 @default.
- W2103240590 cites W2009358874 @default.
- W2103240590 cites W2018986593 @default.
- W2103240590 cites W2020594252 @default.
- W2103240590 cites W2022734924 @default.
- W2103240590 cites W2042078058 @default.
- W2103240590 cites W2057885248 @default.
- W2103240590 cites W2078812274 @default.
- W2103240590 cites W2079292560 @default.
- W2103240590 cites W2084070887 @default.
- W2103240590 cites W2085161549 @default.
- W2103240590 cites W2088591017 @default.
- W2103240590 cites W2090210724 @default.
- W2103240590 cites W2103363623 @default.
- W2103240590 cites W2120359428 @default.
- W2103240590 cites W2126344303 @default.
- W2103240590 cites W2134766739 @default.
- W2103240590 cites W2155625103 @default.
- W2103240590 cites W2166600438 @default.
- W2103240590 cites W2169862854 @default.
- W2103240590 cites W2315223247 @default.
- W2103240590 cites W2329183729 @default.
- W2103240590 cites W4237769345 @default.
- W2103240590 cites W4323875002 @default.
- W2103240590 cites W81899995 @default.
- W2103240590 doi "https://doi.org/10.1002/lsm.22293" @default.
- W2103240590 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4990457" @default.
- W2103240590 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25655579" @default.
- W2103240590 hasPublicationYear "2015" @default.
- W2103240590 type Work @default.
- W2103240590 sameAs 2103240590 @default.
- W2103240590 citedByCount "63" @default.
- W2103240590 countsByYear W21032405902015 @default.
- W2103240590 countsByYear W21032405902016 @default.
- W2103240590 countsByYear W21032405902017 @default.
- W2103240590 countsByYear W21032405902018 @default.
- W2103240590 countsByYear W21032405902019 @default.
- W2103240590 countsByYear W21032405902020 @default.
- W2103240590 countsByYear W21032405902021 @default.
- W2103240590 countsByYear W21032405902022 @default.
- W2103240590 countsByYear W21032405902023 @default.
- W2103240590 crossrefType "journal-article" @default.
- W2103240590 hasAuthorship W2103240590A5012429566 @default.
- W2103240590 hasAuthorship W2103240590A5014431093 @default.
- W2103240590 hasAuthorship W2103240590A5085162752 @default.
- W2103240590 hasBestOaLocation W21032405902 @default.
- W2103240590 hasConcept C12554922 @default.
- W2103240590 hasConcept C153911025 @default.
- W2103240590 hasConcept C185592680 @default.
- W2103240590 hasConcept C190283241 @default.
- W2103240590 hasConcept C202751555 @default.
- W2103240590 hasConcept C2777459323 @default.
- W2103240590 hasConcept C2778005187 @default.
- W2103240590 hasConcept C2780070996 @default.
- W2103240590 hasConcept C2780381497 @default.
- W2103240590 hasConcept C48349386 @default.
- W2103240590 hasConcept C53227056 @default.
- W2103240590 hasConcept C54355233 @default.
- W2103240590 hasConcept C553184892 @default.
- W2103240590 hasConcept C55493867 @default.
- W2103240590 hasConcept C71924100 @default.
- W2103240590 hasConcept C86803240 @default.
- W2103240590 hasConceptScore W2103240590C12554922 @default.
- W2103240590 hasConceptScore W2103240590C153911025 @default.
- W2103240590 hasConceptScore W2103240590C185592680 @default.
- W2103240590 hasConceptScore W2103240590C190283241 @default.
- W2103240590 hasConceptScore W2103240590C202751555 @default.
- W2103240590 hasConceptScore W2103240590C2777459323 @default.
- W2103240590 hasConceptScore W2103240590C2778005187 @default.
- W2103240590 hasConceptScore W2103240590C2780070996 @default.
- W2103240590 hasConceptScore W2103240590C2780381497 @default.
- W2103240590 hasConceptScore W2103240590C48349386 @default.
- W2103240590 hasConceptScore W2103240590C53227056 @default.
- W2103240590 hasConceptScore W2103240590C54355233 @default.
- W2103240590 hasConceptScore W2103240590C553184892 @default.
- W2103240590 hasConceptScore W2103240590C55493867 @default.
- W2103240590 hasConceptScore W2103240590C71924100 @default.
- W2103240590 hasConceptScore W2103240590C86803240 @default.
- W2103240590 hasIssue "2" @default.
- W2103240590 hasLocation W21032405901 @default.
- W2103240590 hasLocation W21032405902 @default.
- W2103240590 hasLocation W21032405903 @default.
- W2103240590 hasLocation W21032405904 @default.