A high-resolution, confocal laser-scanning microscope and flash photolysis system for physiological studies

被引:56
作者
Parker, I [1 ]
Callamaras, N [1 ]
Wier, WG [1 ]
机构
[1] UNIV MARYLAND,SCH MED,DEPT PHYSIOL,BALTIMORE,MD 21201
关键词
D O I
10.1016/S0143-4160(97)90055-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We describe the construction of a high-resolution confocal laser-scanning microscope, and illustrate its use for studying elementary Ca2+ signalling events in cells. An avalanche photodiode module and simple optical path provide a high efficiency system for detection of fluorescence signals, allowing use of a small confocal aperture giving near diffraction-limited spatial resolution (< 300 nm lateral and < 400 nm axial). When operated in line-scan mode, the maximum temporal resolution is 1 ms, and the associated computer software allows complete flexibility to record line-scans continuously for long (minutes) periods or to obtain any desired pixel resolution in x-y scans. An independent UV irradiation system permits simultaneous photolysis of caged compounds over either a uniform, wide field (are lamp source) or at a tightly focussed spot (frequency-tripled Nd:YAG laser). The microscope thus provides a versatile tool for optical studies of dynamic cellular processes, as well as excellent resolution for morphological studies. The confocal scanner can be added to virtually any inverted microscope for a component cost that is only a small fraction of that of comparable commercial instruments, yet offers better performance and greater versatility.
引用
收藏
页码:441 / 452
页数:12
相关论文
共 14 条
[1]   RANGE OF MESSENGER ACTION OF CALCIUM-ION AND INOSITOL 1,4,5-TRISPHOSPHATE [J].
ALLBRITTON, NL ;
MEYER, T ;
STRYER, L .
SCIENCE, 1992, 258 (5089) :1812-1815
[2]  
Art Jonathan, 1995, P183
[3]   THE ELEMENTAL PRINCIPLES OF CALCIUM SIGNALING [J].
BOOTMAN, MD ;
BERRIDGE, MJ .
CELL, 1995, 83 (05) :675-678
[4]  
CHENG H, 1993, SCIENCE, V268, P1045
[5]  
Inoue Shinya, 1995, P1
[6]  
Lerner EJ, 1996, LASER FOCUS WORLD, V32, P93
[7]   LOCAL, STOCHASTIC RELEASE OF CA2+ IN VOLTAGE-CLAMPED RAT-HEART CELLS - VISUALIZATION WITH CONFOCAL MICROSCOPY [J].
LOPEZLOPEZ, JR ;
SHACKLOCK, PS ;
BALKE, CW ;
WIER, WG .
JOURNAL OF PHYSIOLOGY-LONDON, 1994, 480 :21-29
[8]  
MACGREGOR A, 1993, PHOTONICS DESIGN APP, pH111
[9]   Ca2+ sparks involving multiple Ca2+ release sites along Z-lines in rat heart cells [J].
Parker, I ;
Zang, WJ ;
Wier, WG .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 497 (01) :31-38
[10]   Ca2+ transients associated with openings of inositol trisphosphate-gated channels in Xenopus oocytes [J].
Parker, I ;
Yao, Y .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 491 (03) :663-668