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J Dent Res 83(2): 104-108, 2004
© 2004 International and American Associations for Dental Research


RESEARCH REPORT
Biomaterials & Bioengineering

Blue Light Differentially Modulates Cell Survival and Growth

J.C. Wataha1,*, J.B. Lewis1, P.E. Lockwood1, S. Hsu1, R.L. Messer1, F.A. Rueggeberg1, and S. Bouillaguet2

1 Department of Oral Rehabilitation, Medical College of Georgia School of Dentistry, Augusta, GA 30912-1260; and
2 University of Geneva School of Dental Medicine, Geneva, Switzerland;

* corresponding author, watahaj{at}mail.mcg.edu

Previous studies have reported that blue light (400–500 nm) inhibits cell mitochondrial activity. We investigated the hypothesis that cells with high energy consumption are most susceptible to blue-light-induced mitochondrial inhibition. We estimated cell energy consumption by population doubling time, and cell survival and growth by succinate dehydrogenase (SDH) activity. Six cell types were exposed to 5 or 60 J/cm2 of blue light from quartz-tungsten-halogen (QTH), plasma-arc (PAC), or argon laser sources in monolayer culture. Post-light SDH activity correlated positively with population doubling time (R2 = 0.91 for PAC, 0.76 for QTH, 0.68 for laser); SDH activity increased for cell types with the longest doubling times and was suppressed for cell types with shorter doubling times. Thus, light-induced exposure differentially affects SDH activity, cell survival, and growth, depending on cell energy consumption. Blue light may be useful as a therapeutic modulator of cell growth and survival.

KEY WORDS: visible light • in vitro • MTT • fibroblasts • keratinocytes







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