Friedl Peter, Wolf Katarina, von Andrian Ulrich H, Harms Gregory
University of Würzburg, Würzburg, Germany.
Curr Protoc Cell Biol. 2007 Mar;Chapter 4:Unit 4.15. doi: 10.1002/0471143030.cb0415s34.
Multiphoton microscopy has become a standard method for noninvasive imaging of thick specimens with subcellular resolution. Higher harmonic generation microscopy (HHGM), based on nonlinear multiphoton excitation, is a contrast mechanism for the structural and molecular imaging of native samples in cell culture and in fixed and live tissues, for both, three-dimensional and four-dimensional reconstructions. HHGM comprises second and third harmonic generation (SHG, THG) of ordered molecules, can be obtained without exogenous labels, and provides detailed real-time optical reconstruction of fibrillar collagen, myosin, microtubules, and membrane potential, as well as cell depolarization. This unit presents the principles of SHG and THG and the basic setup of a HHGM system, and summarizes current applications in cell biology. Multimodal multiphoton microscopy using HHGM together with two-photon excited fluorescence will develop into a key approach to real-time imaging of cell dynamics in the context of live tissues.
多光子显微镜已成为一种用于对厚标本进行亚细胞分辨率无创成像的标准方法。基于非线性多光子激发的高次谐波产生显微镜(HHGM)是一种用于细胞培养以及固定和活体组织中天然样品的结构和分子成像的对比机制,可用于三维和四维重建。HHGM包括有序分子的二次和三次谐波产生(SHG、THG),无需外源性标记即可获得,并能提供纤维状胶原蛋白、肌球蛋白、微管和膜电位以及细胞去极化的详细实时光学重建。本单元介绍了SHG和THG的原理以及HHGM系统的基本设置,并总结了当前在细胞生物学中的应用。将HHGM与双光子激发荧光结合使用的多模态多光子显微镜将发展成为在活体组织背景下对细胞动态进行实时成像的关键方法。