Principles of multiphoton microscopy

被引:65
作者
Dunn, Kenneth W. [1 ]
Young, Pamela A. [1 ]
机构
[1] Indiana Univ, Sch Med, Div Nephrol, Dept Med, Indianapolis, IN 46202 USA
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2006年 / 103卷 / 02期
关键词
multiphoton microscopy; fluorescence; in vivo imaging; three-dimensional imaging; intravital microscopy;
D O I
10.1159/000090614
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Multiphoton fluorescence microscopy is a powerful, important tool in biomedical research that offers low photon toxicity and higher spatial and temporal resolution than other in vivo imaging modalities. The capability to collect images hundreds of micrometers into biological tissues provides an invaluable tool for studying cellular and subcellular processes in the context of tissues and organs in living animals. Multiphoton microscopy is based upon two-photon excitation of fluorescence that occurs only in a sub-femtoliter volume at the focus; by scanning the focus through a sample, 2- and 3-dimensional images can be collected. The complex 3-dimensional organization of the kidney makes it especially appropriate for multiphoton microscopic analysis, which has been used to characterize numerous aspects of renal physiology and pathophysiology in living rats and mice. However, the ability to collect fluorescence images deep into biological tissues raises unique problems not encountered in other forms of optical microscopy, including issues of probe access, and tissue optics. Future improvements in multiphoton fluorescence microscopy will involve optimizing objectives for the unique characteristics of multiphoton fluorescence imaging, improving the speed at which images may be collected and extending the depth to which imaging may be conducted. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:E33 / E40
页数:8
相关论文
共 43 条
[1]   Time-multiplexed multifocal multiphoton microscope [J].
Andresen, V ;
Egner, A ;
Hell, SW .
OPTICS LETTERS, 2001, 26 (02) :75-77
[2]  
[Anonymous], CONFOCAL 2 PHOTON MI
[3]   In vivo measurement of gene expression, angiogenesis and physiological function in tumors using multiphoton laser scanning microscopy [J].
Brown, EB ;
Campbell, RB ;
Tsuzuki, Y ;
Xu, L ;
Carmeliet, P ;
Fukumura, D ;
Jain, RK .
NATURE MEDICINE, 2001, 7 (07) :864-868
[4]   Multiphoton excitation provides optical sections from deeper within scattering specimens than confocal imaging [J].
Centonze, VE ;
White, JG .
BIOPHYSICAL JOURNAL, 1998, 75 (04) :2015-2024
[5]   APPLICATION OF A FEMTOSECOND SELF-SUSTAINING MODE-LOCKED TI-SAPPHIRE LASER TO THE FIELD OF LASER SCANNING CONFOCAL MICROSCOPY [J].
CURLEY, PF ;
FERGUSON, AI ;
WHITE, JG ;
AMOS, WB .
OPTICAL AND QUANTUM ELECTRONICS, 1992, 24 (08) :851-859
[6]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[7]   Photon upmanship: Why multiphoton imaging is more than a gimmick [J].
Denk, W ;
Svoboda, K .
NEURON, 1997, 18 (03) :351-357
[8]  
DUNN K, 2002, AM J PHYSIOL, V282, pC905
[9]   Comparison of the axial resolution of practical Nipkow-disk confocal fluorescence microscopy with that of multifocal multiphoton microscopy: theory and experiment [J].
Egner, A ;
Andresen, V ;
Hell, SW .
JOURNAL OF MICROSCOPY, 2002, 206 (01) :24-32
[10]   Video-rate scanning two-photon excitation fluorescence microscopy and ratio imaging with cameleons [J].
Fan, GY ;
Fujisaki, H ;
Miyawaki, A ;
Tsay, RK ;
Tsien, RY ;
Ellisman, MH .
BIOPHYSICAL JOURNAL, 1999, 76 (05) :2412-2420