4.8 Article

Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0832308100

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Funding

  1. NCI NIH HHS [R56 CA096823, R01 CA096823, BC991016, PC010342, CA96823-01] Funding Source: Medline
  2. NIA NIH HHS [AG08487, R01 AG008487] Funding Source: Medline
  3. NIBIB NIH HHS [9-P41-EB0011976-16] Funding Source: Medline
  4. PHS HHS [R33-645644] Funding Source: Medline

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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, in-doleamines, 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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