2022 CAP Congress / Congrès de l'ACP 2022

Near-Infrared Photobiomodulation of Living Cells, Tubulin, and Microtubules in Vitro

7 Jun 2022, 09:15

15m

MDCL 1110 (McMaster University)

Oral (Non-Student) / Orale (non-étudiant(e)) Symposia Day (DPMB) - Advances in Biological and Medical Physics Symposium T1-1 Advances in Physics in Biology and Medicine Symp.: Protein system dynamics (DPMB) | Symposium sur les progrès en physique dans la biologie et la médecine: dynamique des systèmes de protéines (DPMB)

Speaker

Dr Michael Staelens (University of Alberta)

Description

We report the results of experimental investigations involving photobiomodulation (PBM) of living cells, tubulin, and microtubules in buffer solutions exposed to near-infrared (NIR) light emitted from an $810$ nm LED with a power density of $25$ mW/cm${}^2$ pulsed at a frequency of $10$ Hz. In the first group of experiments, we measured changes in the alternating current (AC) ionic conductivity in the $50$ - $100$ kHz range of HeLa and U251 cancer cell lines as living cells, exposed to PBM for $60$ minutes, and observed increased resistance compared to the control experiments. In the second group of experiments we investigated the stability and polymerization of microtubules under exposure to PBM. The protein buffer solution used was a mixture of Britton-Robinson buffer (BRB80 aka PEM) and microtubule cushion buffer. Exposure of Taxol™-stabilized microtubules ($\sim 2$ $\mu$M tubulin) to the LED for $120$ minutes, resulted in gradual disassembly of microtubules observed in fluorescence microscopy images. These results were compared to controls where microtubules remained stable. In the third group of experiments we performed turbidity measurements (absorbance readings at $340$ nm) throughout the tubulin polymerization process to quantify the rate and amount of polymerization for exposed versus unexposed tubulin samples, using tubulin re-suspended to final concentrations of $\sim 22.7$ $\mu$M and $\sim 45.5$ $\mu$M in the same buffer solution as before. Compared to the unexposed control samples, absorbance measurement results demonstrated a slower rate and reduced overall amount of polymerization in the less concentrated tubulin samples exposed to PBM for $30$ minutes with the same parameters mentioned above. Paradoxically, the opposite effect was observed in the $45.5$ $\mu$M tubulin samples, demonstrating a remarkable increase in the polymerization rates and total polymer mass achieved after exposure to PBM. These results on the effects of PBM on living cells, tubulin, and microtubules are novel, further validating the modulating effects of PBM and contributing to designing more effective PBM parameters. Finally, potential consequences for the use of PBM in the context of neurodegenerative diseases are discussed.

Presentation materials

NIR PBM — 2022 CAP Congress (M. Staelens) - 2022-06-06.pdf

NIR PBM — 2022 CAP Congress (M. Staelens, No Sequencing) - 2022-06-07.pdf