In vivo three- and four-photon fluorescence microscopy using a 1.8 µm femtosecond fiber laser system
Hideji Murakoshi, Hiromi Ueda, Ryuichiro Goto, Kosuke Hamada, Yutaro Nagasawa, Takao Fuji
Abstract
Multiphoton microscopy has enabled us to image cellular dynamics in vivo . However, the excitation wavelength for imaging with commercially available lasers is mostly limited between 0.65–1.04 µm. Here we develop a femtosecond fiber laser system that produces ∼150 fs pulses at 1.8 µm. Our system starts from an erbium-doped silica fiber laser, and its wavelength is converted to 1.8 µm using a Raman shift fiber. The 1.8 µm pulses are amplified with a two-stage Tm:ZBLAN fiber amplifier. The final pulse energy is ∼1 µJ, sufficient for in vivo imaging. We successfully observe TurboFP635-expressing cortical neurons at a depth of 0.7 mm from the brain surface by three-photon excitation and Clover-expressing astrocytes at a depth of 0.15 mm by four-photon excitation.