Wide-field two-photon microscopy: features and advantages for biomedical applications

We describe a simple fluorescence microscope based on wide-field two-photon excitation. While still taking advantage of some inherent properties of non-linear (two-photon) microscopy, such as increased penetration depth through tissue and reduced phototoxicity, this approach provides video frame rate imaging, can be easily coupled to fluorescence spectral and lifetime detection modules, and makes efficient use of the high average power currently available from ultrashort pulsed lasers. For a standard histopathology specimen, we were able to identify different structures based on spectral and fluorescence lifetime detection and analysis. We examined the use of 200fs and 2ps pulses from Spectra Physics MaiTai and Tsunami lasers, respectively, with average power ranging from 50mW to 500mW.

[1]  J. Zavadil,et al.  Single cell behavior in metastatic primary mammary tumors correlated with gene expression patterns revealed by molecular profiling. , 2002, Cancer research.

[2]  R. B. Campbell,et al.  In vivo measurement of gene expression, angiogenesis and physiological function in tumors using multiphoton laser scanning microscopy , 2001, Nature Medicine.

[3]  J. Squier,et al.  Widefield multiphoton and temporally decorrelated multifocal multiphoton microscopy. , 2000, Optics express.

[4]  F. Helmchen,et al.  Miniaturized two-photon microscope based on a flexible coherent fiber bundle and a gradient-index lens objective. , 2004, Optics letters.

[5]  D. Ledbetter,et al.  Multicolor Spectral Karyotyping of Human Chromosomes , 1996, Science.

[6]  W. Webb,et al.  Multiphoton fluorescence excitation: new spectral windows for biological nonlinear microscopy. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[7]  A. Zvyagin Multiphoton endoscopy , 2007 .

[8]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[9]  D L Farkas,et al.  Near-simultaneous hemoglobin saturation and oxygen tension maps in mouse brain using an AOTF microscope. , 1997, Biophysical journal.

[10]  Mark J. Miller,et al.  Two-Photon Imaging of Lymphocyte Motility and Antigen Response in Intact Lymph Node , 2002, Science.

[11]  Jack Waters,et al.  Ca2+ imaging in the mammalian brain in vivo. , 2002, European journal of pharmacology.

[12]  W. Webb,et al.  Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[13]  E. Wachman,et al.  AOTF microscope for imaging with increased speed and spectral versatility. , 1997, Biophysical journal.

[14]  Charles L. Lawson,et al.  Solving least squares problems , 1976, Classics in applied mathematics.

[15]  D W Tank,et al.  Direct Measurement of Coupling Between Dendritic Spines and Shafts , 1996, Science.

[16]  J. Kirkwood,et al.  Systemic interferon-alpha (IFN-alpha) treatment leads to Stat3 inactivation in melanoma precursor lesions. , 1999, Molecular medicine.

[17]  Roberto Malinow,et al.  Synaptic calcium transients in single spines indicate that NMDA receptors are not saturated , 1999, Nature.

[18]  S. Hell,et al.  Multifocal multiphoton microscopy. , 1998, Optics letters.