Nucleus Near-Infrared (nNIR) Irradiation of Single A549 Cells Induces DNA Damage and Activates EGFR Leading to Mitochondrial Fission

Cells. 2022 Feb 11;11(4):624. doi: 10.3390/cells11040624.

Abstract

There has been great interest in identifying the biological substrate for light-cell interaction and their relations to cancer treatment. In this study, a near-infrared (NIR) laser is focused into the nucleus (nNIR) or cytoplasm (cNIR) of a single living cell by a high numerical aperture condenser to dissect the novel role of cell nucleus in mediating NIR effects on mitochondrial dynamics of A549 non-small cell lung cancer cells. Our analysis showed that nNIR, but not cNIR, triggered mitochondrial fission in 10 min. In contrast, the fission/fusion balance of mitochondria directly exposed to cNIR does not change. While the same phenomenon is also triggered by single molecular interactions between epidermal growth factor (EGF) and its receptor EGFR, pharmacological studies with cetuximab, PD153035, and caffeine suggest EGF signaling crosstalk to DNA damaging response to mediate rapid mitochondrial fission as a result of nNIR irradiation. These results suggest that nuclear DNA integrity is a novel biological target for cellular response to NIR.

Keywords: PD153035; caffeine; cetuximab; epidermal growth factor receptor (EGFR); mitochondrial dynamic; mitochondrial fragmentation count (MFC); near infrared (NIR).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Cell Nucleus / metabolism
  • DNA Damage*
  • Epidermal Growth Factor / genetics
  • ErbB Receptors* / metabolism
  • Humans
  • Lung Neoplasms*
  • Mitochondrial Dynamics
  • Radiation

Substances

  • Epidermal Growth Factor
  • EGFR protein, human
  • ErbB Receptors