Wavelength-dependent cytokine modulation in metabolically stressed fibroblasts

Authors

  • Samantha Bender University of Florida. College of Dentistry. Department of Restorative Dental Sciences.
  • Sharanya Singh University of Florida. College of Dentistry. Department of Restorative Dental Sciences.
  • Lauren Lamoutte University of Florida. College of Dentistry. Department of Restorative Dental Sciences.
  • Mateus Garcia Rocha University of Florida. College of Dentistry. Department of Restorative Dental Sciences.
  • Shannon M Wallet University of Florida. College of Dentistry. Department of Oral Biology.
  • Margarete Ribeiro da Silva University of Florida. College of Dentistry. Department of Oral Biology.
  • Dayane Oliveira University of Florida. College of Dentistry. Department of Oral Biology.

DOI:

https://doi.org/10.1590/

Keywords:

Inflammatory response, Red-light therapy, Photobiomodulation, Light-curing units

Abstract

Objective  To investigate the effects of blue- and red-light irradiation on MTT reduction and cytokine concentrations in metabolically stressed L929 fibroblast-like cells, as an in vitro model to explore wavelength-associated biological responses relevant to light exposure during restorative treatments. Methodology  L929 fibroblast-like cells were seeded in 96-well black plates with clear, flat bottoms (30,000 cells/well) using Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% fetal bovine serum (FBS). After 24 h, the culture medium was replaced with DMEM containing 0.5% FBS to induce metabolic stress. After an additional 24 h, cells were exposed to either blue (452 nm) or red (633 nm) light at a radiant emittance of 200 mW/cm2 for 10, 20, 30, or 60 s (2, 4, 6, or 12 J/cm2). Cells not exposed to light served as controls. MTT reduction (n=3) and cytokine concentrations (n=8) were analyzed using two-way ANOVA followed by Tukey’s test for multiple comparisons. Results  Normalized MTT reduction was numerically higher after red- than blue-light exposure; however, the effect of wavelength did not reach statistical significance (p=0.059), nor exposure time (p=0.057) or the wavelength-by-time interaction (p=0.337). Cytokine concentrations did not show significant overall effects of wavelength, exposure time, or their interaction. In an exploratory maximum-exposure comparison, TNF-α was higher after 60 s of blue-light than in the no-light control (Tukey-adjusted p=0.029), whereas red light did not differ from the control (p=0.101), and blue and red light did not differ from one another (p=0.812). Conclusions  Under the conditions tested, red light was associated with numerically greater MTT reduction than blue light; however, this difference did not reach statistical significance. Blue light increased TNF-α relative to the no-light control, but the small exploratory cytokine dataset does not establish a wavelength-specific inflammatory response.

Downloads

Download data is not yet available.

References

1- Watts DC. Light-curing dental resin-based composites: how it works and how you can make it work. Front Dent Med. 2023;4:1108316. doi: 10.3389/fdmed.2023.1108316

» https://doi.org/10.3389/fdmed.2023.1108316

2- Kowalska A, Sokolowski J, Bociong K. The photoinitiators used in resin based dental composite-a review and future perspectives. Polymers (Basel). 2021;13(3):470. doi: 10.3390/polym13030470

» https://doi.org/10.3390/polym13030470

3- Harlow JE, Sullivan B, Shortall AC, Labrie D, Price RB. Characterizing the output settings of dental curing lights. J Dent. 2016;44:20-6. doi: 10.1016/j.jdent.2015.10.019

» https://doi.org/10.1016/j.jdent.2015.10.019

4- Oliveira DC, Rocha MG, Correr AB, Ferracane JL, Sinhoreti MA. Effect of beam profiles from different light emission tip types of multiwave light-emitting diodes on the curing profile of resin-based composites. Oper Dent. 2019;44(4):365-78. doi: 10.2341/16-242

» https://doi.org/10.2341/16-242

5- Rocha MG, Oliveira D, Felix C, Roulet JF, Sinhoreti MA, Correr AB. Beam profiling of dental light curing units using different camera-based systems. Eur J Dent. 2022;16(1):64-79. doi: 10.1055/s-0041-1731628

» https://doi.org/10.1055/s-0041-1731628

6- Rocha MG, Roulet JF, Sinhoreti MA, Correr AB, Oliveira D. Light transmittance and depth of cure of a bulk fill composite based on the exposure reciprocity law. Braz Dent J. 2021;32(1):78-84. doi: 10.1590/0103-6440202103842

» https://doi.org/10.1590/0103-6440202103842

7- Marovic D, Danicic P, Bojo G, Par M, Tarle Z. Monowave vs. polywave light - curing units: effect on light transmission of composite without alternative photoinitiators. Acta Stomatol Croat. 2024;58(1):30-8. doi: 10.15644/asc58/1/3

» https://doi.org/10.15644/asc58/1/3

8- Turrioni AP, Basso FG, Alonso JR, de Oliveira CF, Hebling J, Bagnato VS, et al. Transdentinal cell photobiomodulation using different wavelengths. Oper Dent. 2015;40(1):102-11. doi: 10.2341/13-370-L

» https://doi.org/10.2341/13-370-L

9- Almeida LF, Basso FG, Turrioni AP, Souza-Costa CA, Hebling J. Metabolism of odontoblast-like cells submitted to transdentinal irradiation with blue and red LED. Arch Oral Biol. 2017;83:258-64. doi: 10.1016/j.archoralbio.2017.08.004

» https://doi.org/10.1016/j.archoralbio.2017.08.004

10- Singh S, Rocha MG, Silvino A, Wallet SM, Sinhoreti MA, Oliveira D. Influence of wavelength on light transmittance, heat generation and pulpal cellular response across different restorative procedures. J Clin Exp Dent. 2026;18(3):e326-34. doi: 10.4317/jced.63873

» https://doi.org/10.4317/jced.63873

11- Alonso JR, Turrioni AP, Basso FG, Souza Costa CA, Hebling J. Synthesis of dental matrix proteins and viability of odontoblast-like cells irradiated with blue LED. Lasers Med Sci. 2016;31(3):523-30. doi: 10.1007/s10103-016-1889-8

12- Holder MJ, Milward MR, Palin WM, Hadis MA, Cooper PR. Effects of red light-emitting diode irradiation on dental pulp cells. J Dent Res. 2012;91(10):961-6. doi: 10.1177/0022034512456040

» https://doi.org/10.1177/0022034512456040

13- Basso FG, Turrioni AP, Almeida LF, Soares DG, Oliveira CF, Hebling J, et al. Nutritional deprivation and LPS exposure as feasible methods for induction of cellular - a methodology to validate for vitro photobiomodulation studies. J Photochem Photobiol B. 2016;159:205-10. doi: 10.1016/j.jphotobiol.2016.04.001

» https://doi.org/10.1016/j.jphotobiol.2016.04.001

14- Almeida LF, Turrioni AP, Basso FG, Montoro LA, Souza-Costa CA, Hebling J. Red LED photobiomodulates the metabolic activity of odontoblast-like cells. Braz Dent J. 2016;27(4):375-80. doi: 10.1590/0103-6440201600152

» https://doi.org/10.1590/0103-6440201600152

15- Ghasemi M, Turnbull T, Sebastian S, Kempson I. The MTT assay: utility, limitations, pitfalls, and interpretation in bulk and single-cell analysis. Int J Mol Sci. 2021;22(23):12827. doi: 10.3390/ijms222312827

» https://doi.org/10.3390/ijms222312827

16- Ragain JC Jr, Brodine BA, Zheng Q, Blen BJ, Garcia-Godoy F, Zhang YH. Effects of curing lights on human gingival epithelial cell proliferation. J Am Dent Assoc. 2021;152(4):260-8. doi: 10.1016/j.adaj.2020.12.006

» https://doi.org/10.1016/j.adaj.2020.12.006

17- Volpato LE, Oliveira RC, Espinosa MM, Bagnato VS, Machado MA. Viability of fibroblasts cultured under nutritional stress irradiated with red laser, infrared laser, and red light-emitting diode. J Biomed Opt. 2011;16(7):075004. doi: 10.1117/1.3602850

18- Mignon C, Uzunbajakava NE, Raafs B, Botchkareva NV, Tobin DJ. Photobiomodulation of human dermal fibroblasts in vitro: decisive role of cell culture conditions and treatment protocols on experimental outcome. Sci Rep. 2017;7(1):2797. doi: 10.1038/s41598-017-02802-0

» https://doi.org/10.1038/s41598-017-02802-0

19- Vinck EM, Cagnie BJ, Cornelissen MJ, Declercq HA, Cambier DC. Increased fibroblast proliferation induced by light emitting diode and low power laser irradiation. Lasers Med Sci. 2003;18(2):95-9. doi: 10.1007/s10103-003-0262-x

» https://doi.org/10.1007/s10103-003-0262-x

20- Opländer C, Hidding S, Werners FB, Born M, Pallua N, Suschek CV. Effects of blue light irradiation on human dermal fibroblasts. J Photochem Photobiol B. 2011;103(2):118-25. doi: 10.1016/j.jphotobiol.2011.02.018

» https://doi.org/10.1016/j.jphotobiol.2011.02.018

21- Mamalis A, Garcha M, Jagdeo J. Light emitting diode-generated blue light modulates fibrosis characteristics: fibroblast proliferation, migration speed, and reactive oxygen species generation. Lasers Surg Med. 2015;47(2):210-5. doi: 10.1002/lsm.22293

» https://doi.org/10.1002/lsm.22293

22- Krassovka JM, Suschek CV, Prost M, Grotheer V, Schiefer JL, Demir E, et al. The impact of non-toxic blue light (453 nm) on cellular antioxidative capacity, TGF-ß1 signaling, and myofibrogenesis of human skin fibroblasts. J Photochem Photobiol B. 2020;209:111952. doi: 10.1016/j.jphotobiol.2020.111952

» https://doi.org/10.1016/j.jphotobiol.2020.111952

23- Brüning AK, Schiefer JL, Fuchs PC, Petzsch P, Köhrer K, Suschek CV, et al. Low-dose blue light (420 nm) reduces metabolic activity and inhibits proliferation of human dermal fibroblasts. Life (Basel). 2023;13(2):331. doi: 10.3390/life13020331

» https://doi.org/10.3390/life13020331

24- Mahmoud NN, Hamad K, Al Shibitini A, Juma S, Sharifi S, Gould L, et al. Investigating inflammatory markers in wound healing: understanding implications and identifying artifacts. ACS Pharmacol Transl Sci. 2024;7(1):18-27. doi: 10.1021/acsptsci.3c00336

» https://doi.org/10.1021/acsptsci.3c00336

25- Idriss HT, Naismith JH. TNF alpha and the TNF receptor superfamily: structure-function relationship(s). Microsc Res Tech. 2000;50(3):184–95. doi: 10.1002/1097-0029(20000801)50:3<184:AID-JEMT2>3.0.CO;2-H

26- Deshmane SL, Kremlev S, Amini S, Sawaya BE. Monocyte chemoattractant protein-1 (MCP-1): an overview. J Interferon Cytokine Res. 2009;29(6):313-26. doi: 10.1089/jir.2008.0027

» https://doi.org/10.1089/jir.2008.0027

27- Harlow JE, Rueggeberg FA, Labrie D, Sullivan B, Price RB. Transmission of violet and blue light through conventional (layered) and bulk cured resin-based composites. J Dent. 2016;53:44-50. doi: 10.1016/j.jdent.2016.06.007

» https://doi.org/10.1016/j.jdent.2016.06.007

28- Singh S, Rocha MG, Wallet SM, Roulet JF, Sinhoreti MA, Oliveira D. Effect of wavelength and radiant emittance on light transmittance and temperature increase in dental resin-based composites. J Appl Oral Sci. 2025;33:e20250307. doi: 10.1590/1678-7757-2025-0307

» https://doi.org/10.1590/1678-7757-2025-0307

Downloads

Published

2026-10-19

Issue

Section

Original Articles

How to Cite

Bender, S., Singh, S., Lamoutte, L., Rocha, M. G., Wallet, S. M., Silva, M. R. da, & Oliveira, D. (2026). Wavelength-dependent cytokine modulation in metabolically stressed fibroblasts. Journal of Applied Oral Science, 34. https://doi.org/10.1590/