Intravital deep-tumor single-beam 3-photon, 4-photon, and harmonic microscopy

Elife. 2022 Feb 15:11:e63776. doi: 10.7554/eLife.63776.

Abstract

Three-photon excitation has recently been demonstrated as an effective method to perform intravital microscopy in deep, previously inaccessible regions of the mouse brain. The applicability of 3-photon excitation for deep imaging of other, more heterogeneous tissue types has been much less explored. In this work, we analyze the benefit of high-pulse-energy 1 MHz pulse-repetition-rate infrared excitation near 1300 and 1700 nm for in-depth imaging of tumorous and bone tissue. We show that this excitation regime provides a more than 2-fold increased imaging depth in tumor and bone tissue compared to the illumination conditions commonly used in 2-photon excitation, due to improved excitation confinement and reduced scattering. We also show that simultaneous 3- and 4-photon processes can be effectively induced with a single laser line, enabling the combined detection of blue to far-red fluorescence together with second and third harmonic generation without chromatic aberration, at excitation intensities compatible with live tissue imaging. Finally, we analyze photoperturbation thresholds in this excitation regime and derive setpoints for safe cell imaging. Together, these results indicate that infrared high-pulse-energy low-repetition-rate excitation opens novel perspectives for intravital deep-tissue microscopy of multiple parameters in strongly scattering tissues and organs.

Keywords: 3-photon microscopy; bone; cancer biology; cell biology; human; mouse; nonlinear microscopy; third harmonic generation; tumor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone and Bones / diagnostic imaging
  • Brain / diagnostic imaging
  • Cell Line, Tumor
  • Cell Survival / physiology
  • Deep Learning*
  • Fluorescent Dyes / chemistry
  • Image Processing, Computer-Assisted
  • Male
  • Mice
  • Microscopy, Fluorescence, Multiphoton / methods*
  • Neoplasms, Experimental / diagnostic imaging*
  • Second Harmonic Generation Microscopy / methods*

Substances

  • Fluorescent Dyes