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3-photon microscopy for deep-tissue imaging

General idea
Imaging depth in two-photon (2P) microscopy is limited by scattering. At depths beyond 500 µm in a densely stained mouse brain, 2P excitation confinement and signal-to-background ratio are severely degraded. One workaround recently pioneered at Cornell University (Xu et al, Nat Phot 2013) is to use 3-photon excitation with infrared-shifted wavelengths near 1.3 or 1.7 µm. This approach can significantly improve the imaging depth, owing to superior excitation confinement (3P effect) and reduced scattering (infrared effect). We are developing this approach and novel applications.

Dual-color 3-photon microscopy
In collaboration with the Lasers group at IOGS, we introduced a novel dual-color laser source design optimized for 3P excitation; we used it to build a 3-photon microscope capable of exciting simultaneously green (GFP) and red (RFP, dTomato) fluorescent proteins deep inside brain tissue (along with label-free THG signals), and obtained the first 3-photon through-skull images of live adult zebrafish brain.

(a) Novel dual-color laser source optimized for 3P microscopy. (b) Comparison of 2P and 3P in-depth imaging of ex vivo mouse brain tissue. (c) in vivo through-skull 3P/THG imaging of two neural cell populations in an adult zebrafish brain. © CNRS, Inserm, Polytechnique, IOGS, Inst Vision, Inst Pasteur / Springer-Nature. Adapted from Guesmi, Abdeladim et al, Light Sci App 2018.


Dual-color deep-tissue three-photon microscopy with a multiband infrared laser
K. Guesmi, L. Abdeladim, S. Tozer, P. Mahou, T. Kumamoto, K. Jurkus, P. Rigaud, K. Loulier, N. Dray, P. Georges, M. Hanna, J. Livet, W. Supatto, E. Beaurepaire, F. Druon
Light: Science & Applications (2018).

All-fiber femtosecond laser providing 9 nJ, 50 MHz pulses at 1650 nm for three-photon microscopy
P. Cadroas, L. Abdeladim, L. Kotov, M. Likhachev, D. Lipatov, D. Gaponov, A. Hideur, M. Tang, J. Livet, W. Supatto, E. Beaurepaire, S. Février
J. Optics (2017).