Single molecule microscopy in 3D cell cultures and tissues

被引:5
作者
Lauer, Florian M. [1 ]
Kaemmerer, Elke [1 ,2 ]
Meckel, Tobias [1 ]
机构
[1] Tech Univ Darmstadt, Dept Biol, D-64287 Darmstadt, Germany
[2] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Fac Sci & Engn, Brisbane, Qld 4059, Australia
关键词
Single molecule microscopy; 3D cell cultures; Spheroids; Light sheet illumination; HILO illumination; Two-photon microscopy; Multiphoton microscopy; Adaptive optics; HIPPOCAMPAL SLICE CULTURES; EXTRACELLULAR-MATRIX; FOCAL ADHESION; BASEMENT-MEMBRANE; IN-VITRO; FLUORESCENCE MICROSCOPY; CANCER SPHEROIDS; GENE-EXPRESSION; LIVE; LOCALIZATION;
D O I
10.1016/j.addr.2014.10.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
From the onset of the first microscopic visualization of single fluorescent molecules in living cells at the beginning of this century, to the present, almost routine application of single molecule microscopy, the method has well-proven its ability to contribute unmatched detailed insight into the heterogeneous and dynamic molecular world life is composed of. Except for investigations on bacteria and yeast, almost the entire story of success is based on studies on adherent mammalian 2D cell cultures. However, despite this continuous progress, the technique was not able to keep pace with the move of the cell biology community to adapt 3D cell culture models for basic research, regenerative medicine, or drug development and screening. In this review, we will summarize the progress, which only recently allowed for the application of single molecule microscopy to 3D cell systems and give an overview of the technical advances that led to it. While initially posing a challenge, we finally conclude that relevant 3D cell models will become an integral part of the on-going success of single molecule microscopy. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 94
页数:16
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