Multiphoton autofluorescence and second-harmonic generation imaging of the tooth

被引:21
作者
Chen, Min-Huey [1 ,2 ]
Chen, Wei-Liang [3 ]
Sun, Yen [3 ]
Fwu, Peter Tramyeon [3 ]
Dong, Chen-Yuan [3 ]
机构
[1] Natl Taiwan Univ Hosp, Coll Med, Dept Dent, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Med, Sch Dent, Taipei 100, Taiwan
[3] Natl Taiwan Univ, Dept Phys, Taipei 106, Taiwan
关键词
multiphoton autofluorescence; second-harmonic generation (SHG); microscopy; dentistry;
D O I
10.1117/1.2812710
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we used an epi-illuminated multiphoton microscope to image three main components of ex vivo human tooth. In particular, we obtained two-photon excited autofluorescence (AF) and second-harmonic generation (SHG) images of the enamel, dentin, and periodontal ligaments (PLs) and constructed three-dimensional projections of sequentially and axially acquired images. We found that the enamel has a strong two-photon AF signal, clearly revealing the structures of the enamel rods. The dentin, on the other hand, has both AF and SHG signals. The contrast provided by the combination of these two imaging modalities can be used to reveal the structure of peritubular dentin and to distinguish the less mineralized circumpulpal dentins. The SHG and multiphoton AF imaging also showed the structure of the PL and the distribution of cells around the PL, respectively. For comparison, we also obtained scanning electron microscopy images of the enamel, dentin, circumpulpal dentin, and the PL. Our results demonstrate the effectiveness of using multiphoton microscopy to visualize the major constituents of teeth, including enamel, dentin, and the PL, and the potential of this minimally invasive technique for monitoring the morphological developments during tooth regeneration. (C) 2007 Society of Photo-Optical Instrumentation Engineers.
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页数:6
相关论文
共 15 条
[1]  
Avery JK., 2001, ORAL DEV HISTOLOGY, V3rd, DOI DOI 10.1016/j.jsb.2009.02.001
[2]   Dynamic imaging of collagen and its modulation in tumors in vivo using second-harmonic generation [J].
Brown, E ;
McKee, T ;
diTomaso, E ;
Pluen, A ;
Seed, B ;
Boucher, Y ;
Jain, RK .
NATURE MEDICINE, 2003, 9 (06) :796-800
[3]   Second-harmonic imaging microscopy for visualizing biomolecular arrays in cells, tissues and organisms [J].
Campagnola, PJ ;
Loew, LM .
NATURE BIOTECHNOLOGY, 2003, 21 (11) :1356-1360
[4]  
CHEN JC, 2003, CLEO PACIFIC RIM 200
[5]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[6]  
Girkin J. M., 1999, Early detection of dental caries II, P155
[7]  
HALL A, 2004, REV POTENTIAL NEW DI, P89
[8]   Optical biopsy of liver fibrosis by use of multiphoton microscopy [J].
Lee, HS ;
Liu, Y ;
Chen, HC ;
Chiou, LL ;
Huang, GT ;
Lo, W ;
Dong, CY .
OPTICS LETTERS, 2004, 29 (22) :2614-2616
[9]   Evaluating cutaneous photoaging by use of multiphoton fluorescence and second-harmonic generation microscopy [J].
Lin, SJ ;
Wu, RJ ;
Tan, HY ;
Lo, W ;
Lin, WC ;
Young, TH ;
Hsu, CJ ;
Chen, JS ;
Jee, SH ;
Dong, CY .
OPTICS LETTERS, 2005, 30 (17) :2275-2277
[10]  
Piesco NP, 1994, ORAL DEV HISTOLOGY, P242