Third-harmonic generation for the study of Caenorhabditis elegans embryogenesis

被引:35
作者
Aviles-Espinosa, Rodrigo [1 ]
Santos, Susana I. C. O. [1 ]
Brodschelm, Andreas [2 ]
Kaenders, Wilhelm G. [2 ]
Alonso-Ortega, Cesar [1 ]
Artigas, David [1 ,3 ]
Loza-Alvarez, Pablo [1 ]
机构
[1] Inst Ciencies Foton, Inst Photon Sci, Barcelona 08860, Spain
[2] TOPTICA Photon AG, D-82166 Graefelfing, Germany
[3] Univ Politecn Cataluna, Dept Signal Theory & Commun, ES-08034 Barcelona, Spain
基金
芬兰科学院;
关键词
multiphoton processes; nonlinear microscopy; fiber laser; biological imaging; functional monitoring and imaging; three-dimensional microscopy; time-resolved imaging; MORPHOGENETIC MOVEMENTS; CELL LINEAGE; MICROSCOPY;
D O I
10.1117/1.3477535
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Live microscopy techniques (i.e., differential interference contrast, confocal microscopy, etc.) have enabled the understanding of the mechanisms involved in cells and tissue formation. In long-term studies, special care must be taken in order to avoid sample damage, restricting the applicability of the different microscopy techniques. We demonstrate the potential of using third-harmonic generation (THG) microscopy for morphogenesis/embryogenesis studies in living Caenorhabditis elegans (C. elegans). Moreover, we show that the THG signal is obtained in all the embryo development stages, showing different tissue/structure information. For this research, we employ a 1550-nm femtosecond fiber laser and demonstrate that the expected water absorption at this wavelength does not severely compromise sample viability. Additionally, this has the important advantage that the THG signal is emitted at visible wavelengths (516 nm). Therefore, standard collection optics and detectors operating near maximum efficiency enable an optimal signal reconstruction. All this, to the best of our knowledge, demonstrates for the first time the noninvasiveness and strong potential of this particular wavelength to be used for high-resolution four-dimensional imaging of embryogenesis using unstained C. elegans in vivo samples. (C) 2010 Society of Photo-Optical Instrumentation Engineers. [DOI: 10.1117/1.3477535]
引用
收藏
页数:7
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