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Cellular transformations in near-infrared light-induced apoptosis in cancer cells revealed by label-free CARS imaging.
Levchenko, Svitlana M; Kuzmin, Andrey N; Pliss, Artem; Ohulchanskyy, Tymish Y; Prasad, Paras N; Qu, Junle.
Afiliación
  • Levchenko SM; Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, Guangdong, P. R. China.
  • Kuzmin AN; Institute for Lasers, Photonics and Biophotonics, University at Buffalo, State University of New York, Buffalo, New York.
  • Pliss A; Advanced Cytometry Instrumentation Systems, LLC, Buffalo, New York.
  • Ohulchanskyy TY; Institute for Lasers, Photonics and Biophotonics, University at Buffalo, State University of New York, Buffalo, New York.
  • Prasad PN; Advanced Cytometry Instrumentation Systems, LLC, Buffalo, New York.
  • Qu J; Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, Guangdong, P. R. China.
J Biophotonics ; 12(12): e201900179, 2019 12.
Article en En | MEDLINE | ID: mdl-31339662
ABSTRACT
Photobiomodulation (PBM) involves light to activate cellular signaling pathways leading to cell proliferation or death. In this work, fluorescence and Coherent anti-Stokes Raman Scattering (CARS) imaging techniques were applied to assess apoptosis in human cervical cancer cells (HeLa) induced by near infrared (NIR) laser light (808 nm). Using the Caspase 3/7 fluorescent probe to identify apoptotic cells, we found that the pro-apoptotic effect is significantly dependent of irradiation dose. The highest apoptosis rate was noted for the lower irradiation doses, that is, 0.3 J/cm2 (~58%) and 3 J/cm2 (~28%). The impact of light doses on proteins/lipids intracellular metabolism and distribution was evaluated using CARS imaging, which revealed apoptosis-associated reorganization of nuclear proteins and cytoplasmic lipids after irradiation with 0.3 J/cm2 . Doses of NIR light causing apoptosis (0.3, 3 and 30 J/cm2 ) induced a gradual increase in the nuclear protein level over time, in contrast to proteins in cells non-irradiated and irradiated with 10 J/cm2 . Furthermore, irradiation of the cells with the 0.3 J/cm2 dose resulted in lipid droplets (LDs) accumulation, which was apparently caused by an increase in reactive oxygen species (ROS) generation. We suggest that PBM induced apoptosis could be caused by the ability of NIR light to trigger excessive LDs formation which, in turn, induces cellular cytotoxicity.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espectrometría Raman / Transformación Celular Neoplásica / Apoptosis / Imagen Molecular / Rayos Infrarrojos Límite: Humans Idioma: En Revista: J Biophotonics Asunto de la revista: BIOFISICA Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espectrometría Raman / Transformación Celular Neoplásica / Apoptosis / Imagen Molecular / Rayos Infrarrojos Límite: Humans Idioma: En Revista: J Biophotonics Asunto de la revista: BIOFISICA Año: 2019 Tipo del documento: Article