Two-versus one photon excitation laser scanning microscopy: Critical importance of excitation wavelength

被引:43
作者
Bush, Peter G.
Wokosin, David L.
Hall, Andrew C.
机构
[1] Univ Edinburgh, Sch Biomed Sci, Ctr Integrat Physiol, Edinburgh EH8 9XD, Midlothian, Scotland
[2] Univ Strathclyde, Ctr Biophoton, Glasgow G4 0NR, Lanark, Scotland
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2007年 / 12卷
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
2; photon; two photon; non-linear; multiphoton; two-photon laser scanning microscopy; confocal laser microscopy; confocal laser scanning; microscopy; articular cartilage; chondrocyte; cell viability; volume regulation; regulatory volume decrease; image depth; photo-toxicity; photo-bleaching;
D O I
10.2741/2261
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
It is often anticipated that two-photon excitation ( TPE) laser scanning microscopy should improve cell survival and tissue penetration relative to conventional one-photon excitation ( OPE) confocal scanning laser microscopy ( CLSM). However few studies have directly compared live cell imaging using one- vs two-photon laser scanning microscopy. We have used calcein-loaded in situ chondrocytes within cartilage as a model for quantitatively comparing these techniques. TPE reduced photo-bleaching and improved cell viability compared to OPE. Using improved detection sensitivity coupled with increased tissue penetration of the near infra-red TPE laser, it was possible to capture images deeper within the cartilage. However, the advantages of TPE vs OPE were strongly dependent on excitation wavelength. We conclude that optimising TPE conditions is essential for realizing the full benefits of this approach.
引用
收藏
页码:2646 / 2657
页数:12
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