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多光子显微镜原理。

Principles of multiphoton microscopy.

作者信息

Dunn Kenneth W, Young Pamela A

机构信息

Department of Medicine, Division of Nephrology, Indiana University School of Medicine, Indianapolis, Ind 46202, USA.

出版信息

Nephron Exp Nephrol. 2006;103(2):e33-40. doi: 10.1159/000090614. Epub 2006 Mar 10.

Abstract

Multiphoton fluorescence microscopy is a powerful, important tool in biomedical research that offers low photon toxicity and higher spatial and temporal resolution than other in vivo imaging modalities. The capability to collect images hundreds of micrometers into biological tissues provides an invaluable tool for studying cellular and subcellular processes in the context of tissues and organs in living animals. Multiphoton microscopy is based upon two-photon excitation of fluorescence that occurs only in a sub-femtoliter volume at the focus; by scanning the focus through a sample, 2- and 3-dimensional images can be collected. The complex 3-dimensional organization of the kidney makes it especially appropriate for multiphoton microscopic analysis, which has been used to characterize numerous aspects of renal physiology and pathophysiology in living rats and mice. However, the ability to collect fluorescence images deep into biological tissues raises unique problems not encountered in other forms of optical microscopy, including issues of probe access, and tissue optics. Future improvements in multiphoton fluorescence microscopy will involve optimizing objectives for the unique characteristics of multiphoton fluorescence imaging, improving the speed at which images may be collected and extending the depth to which imaging may be conducted.

摘要

多光子荧光显微镜是生物医学研究中一种强大且重要的工具,它具有低光子毒性,并且与其他体内成像方式相比,具有更高的空间和时间分辨率。能够在生物组织中深入数百微米采集图像,为研究活体动物组织和器官环境中的细胞及亚细胞过程提供了一种极为珍贵的工具。多光子显微镜基于荧光的双光子激发,这种激发仅发生在焦点处的亚飞升体积内;通过在样品中扫描焦点,可以采集二维和三维图像。肾脏复杂的三维结构使其特别适合多光子显微镜分析,该技术已被用于表征活体大鼠和小鼠肾脏生理学和病理生理学的诸多方面。然而,在生物组织中深入采集荧光图像的能力引发了其他形式光学显微镜未曾遇到的独特问题,包括探针进入问题和组织光学问题。多光子荧光显微镜未来的改进将包括针对多光子荧光成像的独特特性优化物镜、提高图像采集速度以及扩大成像深度。

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