Time-resolved fluorescence imaging and background rejection by two-photon excitation in laser-scanning microscopy

1992 ◽  
Author(s):  
David W. Piston ◽  
David R. Sandison ◽  
Watt W. Webb
Keyword(s):  
Fluorescence Imaging ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Scanning Microscopy ◽  
Time Resolved Fluorescence ◽  
Time Resolved ◽  
Background Rejection ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

scholarly journals Confocal Laser Scanning Microscopy and Two Photon Excitation Microscopy as Tools to Study Testate Amoebae

2010 ◽  
Vol 16 (S2) ◽  
pp. 1142-1143
Author(s):  
Z Burdíková ◽  
M Čapek ◽  
P Ostasou ◽  
EAD Mitchell ◽  
J Machač ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Testate Amoebae ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Two Photon ◽  
Photon Excitation ◽  
Two Photon Excitation

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.

Quantitative 3D fluorescence technique for the analysis of en face preparations of arterial walls using quantum dot nanocrystals and two-photon excitation laser scanning microscopy

2006 ◽  
Vol 290 (1) ◽  
pp. R114-R123 ◽  
Author(s):  
Dardo E. Ferrara ◽  
Daiana Weiss ◽  
Peter H. Carnell ◽  
Ray P. Vito ◽  
David Vega ◽  
...  
Keyword(s):  
Quantum Dot ◽  
Laser Scanning ◽  
Vascular Tissue ◽  
Laser Scanning Microscopy ◽  
Scanning Microscopy ◽  
Two Photon ◽  
Photon Excitation ◽  
En Face ◽  
Excitation Laser ◽  
Two Photon Excitation

Traditional imaging with one-photon confocal microscopy and organic fluorophores poses several challenges for the visualization of vascular tissue, including autofluorescence, fluorophore crosstalk, and photobleaching. We studied human coronary arteries (HCAs) and mouse aortas with a modified immunohistochemical (IHC) “en face” method using quantum dot (Qdot) bioconjugates and two-photon excitation laser scanning microscopy (TPELSM). We demonstrated the feasibility of multilabeling intimal structures by exciting multicolored Qdots with only one laser wavelength (750 nm). Detailed cell structures, such as the granular appearance of von Willebrand factor (VWF) and the subcellular distribution of endothelial nitric oxide synthase, were visualized using green dots (525 nm), even when the emission maximum of these Qdots overlapped that of tissue autofluorescence (510–520 nm). In addition, sensitive fluorescence quantification of vascular cell adhesion molecule 1 expression at areas of varying hemodynamics (intercostal branches vs. nonbranching areas) was performed in normal C57Bl/6 mice. Finally, we took advantage of the photostability of Qdots and the inherent three-dimensional (3D) resolution of TPELSM to obtain large z-stack series without photobleaching. This innovative en face method allowed simple multicolor profiling, highly sensitive fluorescence quantitation, and 3D visualization of the vascular endothelium with excellent spatial resolution. This is a promising technique to define the spatial and temporal interactions of endothelial inflammatory markers and quantify the effects of different interventions on the endothelium.

scholarly journals Two-Photon Excitation Laser Scanning Microscopy of Human, Porcine, and Rabbit Nasal Septal Cartilage

2001 ◽  
Vol 7 (5) ◽  
pp. 599-606 ◽  
Author(s):  
Brian J.F. Wong ◽  
Vincent Wallace ◽  
Mariah Coleno ◽  
Hilary P. Benton ◽  
Bruce J. Tromberg
Keyword(s):  
Laser Scanning ◽  
Septal Cartilage ◽  
Laser Scanning Microscopy ◽  
Scanning Microscopy ◽  
Two Photon ◽  
Photon Excitation ◽  
Excitation Laser ◽  
Nasal Septal Cartilage ◽  
Two Photon Excitation
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