Multi-photon fluorescence microscopy - the response of plant cells to high intensity illumination

被引:36
作者
Cheng, PC
Lin, BL [1 ]
Kao, FJ
Gu, M
Xu, MG
Gan, XS
Huang, MK
Wang, YS
机构
[1] Acad Sinica, Inst Mol Biol, Taipei 11529, Taiwan
[2] SUNY Buffalo, Dept Elect Engn, Adv Microscopy & Imaging Lab, Buffalo, NY 14260 USA
[3] Natl Sun Yat Sen Univ, Dept Phys, Kaohsiung 80424, Taiwan
[4] Swinburne Univ Technol, Sch Biophys Sci & Elect Engn, Ctr Microphoton, Hawthorn, Vic 3122, Australia
基金
澳大利亚研究理事会;
关键词
two-photon fluorescence microscopy; cell damage; absorption; scattering; auto-fluorescence; Arabidopsis; plant cell; protoplast;
D O I
10.1016/S0968-4328(00)00068-8
中图分类号
TH742 [显微镜];
学科分类号
摘要
Multi-photon fluorescence microscopy has been cited for its advantage in increased depth penetration due to low linear absorption and scattering coefficient of biological specimen in the near infrared (NIR) range. Because of the need of high peak power for efficiently exciting two-photon fluorescence, the relationship between cell damage and peak power has become an interesting and much debated topic in the applications of multi-photon fluorescence microscopy. It is conceivable that at high illumination intensity, non-linear photochemical processes have impacts on cell physiology and viability in ways much different from low illumination in the linear domain. In this article, we discuss some of the issues in two-photon fluorescence microscopy, including the degree of transparency of the specimen, a comparison of single- and two-photon excited fluorescence spectra, and the cell damage under high intensity illumination, using plant cells as a model. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:661 / 669
页数:9
相关论文
共 44 条
[1]  
Bhawalkar J. D., 1996, Bioimaging, V4, P168, DOI 10.1002/1361-6374(199609)4:3<168::AID-BIO7>3.3.CO
[2]  
2-#
[3]  
BHAWALKAR JD, 1997, POLYM COMMUN, V38, P451
[4]  
Cheng PC, 1998, J MICROSC-OXFORD, V189, P199, DOI 10.1046/j.1365-2818.1998.00277.x
[5]  
CHENG PC, 2000, SCANNING, V22, P187
[6]  
CHENG PC, 1996, SCANNING, V18, P148
[7]  
CHENG PC, 1996, SCANNING, V18, P129
[8]  
CHENG PC, 2000, SPIE P, V4082, P134
[9]  
CHENG PC, 2000, MICROSC MICROANAL, V6, P820
[10]  
CHENG PC, 2000, SPIE P, V4082, P87