Takamatsu T, Fujita S
Department of Pathology, Kyoto Prefectural University of Medicine.
Nihon Rinsho. 1992 Oct;50(10):2542-6.
By using a focused laser beam as the light source of the microscope, to minimized flare, together with a pinhole in front of a photo detector to eliminate out-of-focus data, the confocal laser scanning microscope (CLSM) provides a depth-discriminated fluorescence image with high spatial resolution. The CLSM, therefore, has been widely used as a tool for accurate morphometric and densitometric analyses. We discussed here the biological applications of CLSM for demonstrating the three-dimensional features of the embryonic heart tube and chromosome and for imaging fast dynamic changes of [Ca2+]i in the living heart muscle cell pairs.
通过使用聚焦激光束作为显微镜的光源以最小化光斑,并在光探测器前设置针孔以消除离焦数据,共聚焦激光扫描显微镜(CLSM)提供了具有高空间分辨率的深度分辨荧光图像。因此,CLSM已被广泛用作精确形态计量和光密度分析的工具。我们在此讨论CLSM在生物学上的应用,用于展示胚胎心脏管和染色体的三维特征,以及对活心肌细胞对中[Ca2+]i的快速动态变化进行成像。