Imaging developing neural morphology using optical coherence tomography

被引:54
作者
Boppart, SA [1 ]
Bouma, BE [1 ]
Brezinski, ME [1 ]
Tearney, GJ [1 ]
Fujimoto, JG [1 ]
机构
[1] HARVARD UNIV,SCH MED,CARDIAC UNIT,MASSACHUSETTS GEN HOSP,BOSTON,MA 02114
关键词
imaging; development; embryology; microscopy; optics; Xenopus laevis;
D O I
10.1016/S0165-0270(96)00104-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Imaging technologies offer numerous possibilities to investigate the processes involved in neural development. The optical coherence tomography (OCT) technology is analogous to ultrasound backscatter microscopy except reflections of light are detected rather than sound. The OCT technology combines high-resolution in vivo imaging in a diode-based benchtop instrument capable of micron-scale resolution in transparent and non-transparent biological specimens, In this paper, we examine the potential of using OCT for the investigation of developing neural morphology. To demonstrate the capabilities of this technique in assessing neural development, we have chosen to image early normal and abnormal neural morphology in a common developmental biology model, Xenopus laevis. In vivo images clearly identify gross and subtle differences in neural structure and may offer an alternative to the costly and time-consuming process of repeated histological preparation for neural developmental studies. Because imaging can be performed rapidly and repeatedly, the morphological changes of single specimens can be followed throughout development. To illustrate the future potential of this technique, a state-of-the-art Cr4+:forsterite modelocked laser is used as a broad bandwidth light source to image individual cells in a developing specimen.
引用
收藏
页码:65 / 72
页数:8
相关论文
共 19 条
[1]   HIGH-RESOLUTION OPTICAL COHERENCE TOMOGRAPHIC IMAGING USING A MODE-LOCKED TI-AL2O3 LASER SOURCE [J].
BOUMA, B ;
TEARNEY, GJ ;
BOPPART, SA ;
HEE, MR ;
BREZINSKI, ME ;
FUJIMOTO, JG .
OPTICS LETTERS, 1995, 20 (13) :1486-1488
[2]   Optical coherence tomography for optical biopsy - Properties and demonstration of vascular pathology [J].
Brezinski, ME ;
Tearney, GJ ;
Bouma, BE ;
Izatt, JA ;
Hee, MR ;
Swanson, EA ;
Southern, JF ;
Fujimoto, JG .
CIRCULATION, 1996, 93 (06) :1206-1213
[3]  
CLIVAZ X, 1994, SPIE P, V2083, P19
[4]   MEASUREMENT OF THE THICKNESS OF FUNDUS LAYERS BY PARTIAL COHERENCE TOMOGRAPHY [J].
DREXLER, W ;
HITZENBERGER, CK ;
SATTMANN, H ;
FERCHER, AF .
OPTICAL ENGINEERING, 1995, 34 (03) :701-710
[5]   OPTICAL BIOPSY AND IMAGING USING OPTICAL COHERENCE TOMOGRAPHY [J].
FUJIMOTO, JG ;
BREZINSKI, ME ;
TEARNEY, GJ ;
BOPPART, SA ;
BOUMA, B ;
HEE, MR ;
SOUTHERN, JF ;
SWANSON, EA .
NATURE MEDICINE, 1995, 1 (09) :970-972
[6]   ACCELERATION OF INTRACELLULAR CALCIUM WAVES IN XENOPUS-OOCYTES BY CALCIUM INFLUX [J].
GIRARD, S ;
CLAPHAM, D .
SCIENCE, 1993, 260 (5105) :229-232
[7]   OPTICAL COHERENCE TOMOGRAPHY OF THE HUMAN RETINA [J].
HEE, MR ;
IZATT, JA ;
SWANSON, EA ;
HUANG, D ;
SCHUMAN, JS ;
LIN, CP ;
PULIAFITO, CA ;
FUJIMOTO, JG .
ARCHIVES OF OPHTHALMOLOGY, 1995, 113 (03) :325-332
[8]   OPTICAL COHERENCE TOMOGRAPHY [J].
HUANG, D ;
SWANSON, EA ;
LIN, CP ;
SCHUMAN, JS ;
STINSON, WG ;
CHANG, W ;
HEE, MR ;
FLOTTE, T ;
GREGORY, K ;
PULIAFITO, CA ;
FUJIMOTO, JG .
SCIENCE, 1991, 254 (5035) :1178-1181
[9]   MAGNETIC-RESONANCE MICROSCOPY OF EMBRYONIC-CELL LINEAGES AND MOVEMENTS [J].
JACOBS, RE ;
FRASER, SE .
SCIENCE, 1994, 263 (5147) :681-684
[10]   IMAGING NEURONAL DEVELOPMENT WITH MAGNETIC-RESONANCE-IMAGING (NMR) MICROSCOPY [J].
JACOBS, RE ;
FRASER, SE .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 54 (02) :189-196