Multi-photon excitation imaging of dynamic processes in living cells and tissues

被引:36
作者
Benninger, R. K. P. [1 ]
Hao, M. [1 ]
Piston, D. W. [1 ]
机构
[1] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
来源
REVIEWS OF PHYSIOLOGY, BIOCHEMISTRY AND PHARMACOLOGY, VOL 160 | 2008年 / 160卷
关键词
two-photon microscopy; optical sectioning; fluorescence; intra-vital imaging; photoactivation; ablation; intrinsic fluorophores; second harmonic generation;
D O I
10.1007/112_2008_801
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Over the past decade, two-photon microscopy has successfully made the transition from the laser laboratory into a true biological research setting. This has been due in part to the recent development of turnkey ultrafast laser systems required for two-photon microscopy, allowing ease of use in nonspecialist laboratories. The advantages of two-photon microscopy over conventional optical sectioning techniques are for greater imaging depths and reduced overall phototoxicity, as such enabling noninvasive intra-vital imaging of cellular and subcellular processes. Greater understanding of these advantages has allowed this technique to be more effectively utilized in a biological research setting. This review will cover the recent widespread uses of two-photon microscopy and highlight the wide range of physiological studies enabled in fields such as neurosciences, developmental biology, immunology, cancer biology, and endocrinology.
引用
收藏
页码:71 / 92
页数:22
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