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

被引:1474
作者
Zipfel, WR
Williams, RM
Christie, R
Nikitin, AY
Hyman, BT
Webb, WW [1 ]
机构
[1] Cornell Univ, Dept Appl & Engn Phys, Ithaca, NY 14853 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Charlestown, MA 02129 USA
[3] Cornell Univ, Dept Biomed Sci, Ithaca, NY 14853 USA
关键词
D O I
10.1073/pnas.0832308100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:7075 / 7080
页数:6
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