Centre for Microscopy Research (CMO), Department of Cell Biology and Histology, Academic Medical Centre, Amsterdam, The Netherlands.
J Microsc. 2010 Dec;240(3):197-206. doi: 10.1111/j.1365-2818.2010.03400.x.
Phototoxicity and photobleaching are major limitations of fluorescence live-cell microscopy. A straightforward way to limit phototoxicity and photobleaching is reduction of the excitation light dose, but this causes loss of image quality. In confocal fluorescence microscopy, the field of view is illuminated uniformly whereas in controlled light exposure microscopy, illumination is controlled per pixel on the basis of two illumination strategies. The controlled light exposure microscopy foreground strategy discriminates between bright and weak foreground. Bright foreground pixels are illuminated with a reduced light dose resulting in limited excitation of fluorophores and consequently limited phototoxicity and photobleaching. The controlled light exposure microscopy background strategy discriminates between foreground and background. Pixels that are judged to be background are also illuminated with a reduced light dose. The latter illumination strategy may introduce artefacts due to the stochastic character of photon flow. These artefacts are visible as erratic 'darker pixels' in the foreground with a lower pixel value than the neighbouring pixels. This paper describes a special adaptive image processing filter that detects and corrects most of the 'darker pixels'. It opens the possibility to use controlled light exposure microscopy even in high noise (low signal to noise ratio) imaging to further reduce phototoxicity and photobleaching.
光毒性和光漂白是荧光活细胞显微镜的主要限制因素。减少激发光剂量是限制光毒性和光漂白的一种简单方法,但这会导致图像质量下降。在共聚焦荧光显微镜中,视场被均匀照亮,而在受控光暴露显微镜中,根据两种照明策略逐像素控制照明。受控光暴露显微镜前景策略区分亮前景和弱前景。亮前景像素用减少的光剂量照射,导致荧光团的有限激发,从而限制光毒性和光漂白。受控光暴露显微镜背景策略区分前景和背景。被判断为背景的像素也用减少的光剂量照射。由于光子流的随机性,后一种照明策略可能会引入伪影。这些伪影表现为前景中不规则的“较暗像素”,其像素值比相邻像素低。本文描述了一种特殊的自适应图像处理滤波器,它可以检测和校正大多数“较暗像素”。它为使用受控光暴露显微镜打开了可能性,即使在高噪声(低信噪比)成像中,也可以进一步降低光毒性和光漂白。