Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation
Author(s) -
Warren R. Zipfel,
Rebecca M. Williams,
Richard H. Christie,
Alexander Yu. Nikitin,
Bradley T. Hyman,
Watt W. Webb
Publication year - 2003
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0832308100
Subject(s) - microscopy , nicotinamide adenine dinucleotide , fluorescence , two photon excitation microscopy , fluorescence microscope , second harmonic generation , fluorescence lifetime imaging microscopy , excited state , biophysics , high harmonic generation , chemistry , materials science , optics , biology , nad+ kinase , laser , biochemistry , physics , atomic physics , enzyme
Multicolor nonlinear microscopy of living tissue using two- and three-photon-excited intrinsic fluorescence combined with second harmonic generation by supermolecular structures produces images with the resolution and detail of standard histology without the use of exogenous stains. Imaging of intrinsic indicators within tissue, such as nicotinamide adenine dinucleotide, retinol, indoleamines, and collagen provides crucial information for physiology and pathology. The efficient application of multiphoton microscopy to intrinsic imaging requires knowledge of the nonlinear optical properties of specific cell and tissue components. Here we compile and demonstrate applications involving a range of intrinsic molecules and molecular assemblies that enable direct visualization of tissue morphology, cell metabolism, and disease states such as Alzheimer's disease and cancer.
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