Low level laser therapy activates NF-kB via generation of reactive oxygen species in mouse embryonic fibroblasts

Aaron Chih Hao Chen, Praveen R. Arany, Ying Ying Huang, Elizabeth M. Tomkinson, Taimur Saleem, Fiona E. Yull, Timothy S. Blackwell, Michael R. Hamblm

Research output: Contribution to journalConference articlepeer-review

28 Citations (Scopus)

Abstract

Despite over forty years of investigation on low-level light therapy (LLLT), the fundamental mechanisms underlying photobiomodulation remain unclear. In this study, we isolated murine embryonic fibroblasts (MEF) from transgenic NF-kB luciferase reporter mice and studied their response to 810-nm laser radiation. Significant activation of NF-kB was observed for fluences higher than 0.003 J/cm2. NF-kB activation by laser was detectable at 1-hour time point. Moreover, we demonstrated that laser phosphorylated both IKK α/β and NF-kB 15 minutes after irradiation, which implied that laser activates NF-kB via phosphorylation of IKK α/β. Suspecting mitochondria as the source of NF-kB activation signaling pathway, we demonstrated that laser increased both intracellular reactive oxygen species (ROS) by fluorescence microscopy with dichlorodihydrofluorescein and ATP synthesis by luciferase assay. Mitochondrial inhibitors, such as antimycin A, rotenone and paraquat increased ROS and NF-kB activation but had no effect on ATP. The ROS quenchers N-acetyl-L-cysteine and ascorbic acid abrogated laser-induced NF-kB and ROS but not ATP. These results suggested that ROS might play an important role in the signaling pathway of laser induced NF-kB activation. However, the western blot showed that antimycin A, a mitochondrial inhibitor, did not activate NF-kB via serine phosphorylation of IKK α/β as the laser did. On the other hand, LLLT, unlike mitochondrial inhibitors, induced increased cellular ATP levels, which indicates that light also upregulates mitochondrial respiration. ATP upregulation reached a maximum at 0.3 J/cm2 or higher. We conclude that LLLT not only enhances mitochondrial respiration, but also activates the redox-sensitive transcription factor NF-kB by generating ROS as signaling molecules.

Original languageEnglish
Article number71650B
JournalProgress in Biomedical Optics and Imaging - Proceedings of SPIE
Volume7165
DOIs
Publication statusPublished - 2009
Externally publishedYes
EventMechanisms for Low-Light Therapy IV - San Jose, CA, United States
Duration: 24 Jan 200924 Jan 2009

Keywords

  • Low level laser therapy
  • Luciferase reporter mice
  • NF-kB transcription factor
  • Photobiomudulation
  • Reactive oxygen species

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Atomic and Molecular Physics, and Optics
  • Biomaterials
  • Radiology, Nuclear Medicine and Imaging

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