Sacconi L, Tolic-Nørrelykke I M, D'Amico M, Vanzi F, Olivotto M, Antolini R, Pavone F S
European Laboratory for Non-Linear Spectroscopy, via Nello Carrara 1, I-50019 Sesto Fiorentino, Florence, Italy.
Cell Biochem Biophys. 2006;45(3):289-302. doi: 10.1385/CBB:45:3:289.
Advances in the technologies for labeling and imaging biological samples drive a constant progress in our capability of studying structures and their dynamics within cells and tissues. In the last decade, the development of numerous nonlinear optical microscopies has led to a new prospective both in basic research and in the potential development of very powerful noninvasive diagnostic tools. These techniques offer large advantages over conventional linear microscopy with regard to penetration depth, spatial resolution, three-dimensional optical sectioning, and lower photobleaching. Additionally, some of these techniques offer the opportunity for optically probing biological functions directly in living cells, as highlighted, for example, by the application of second harmonic generation to the optical measurement of electrical potential and activity in excitable cells. In parallel with imaging techniques, nonlinear microscopy has been developed into a new area for the selective disruption and manipulation of intracellular structures, providing an extremely useful tool of investigation in cell biology. In this review we present some basic features of nonlinear microscopy with regard both to imaging and manipulation, and show some examples to illustrate the advantages offered by these novel methodologies.
生物样品标记和成像技术的进步推动了我们在研究细胞和组织内结构及其动态方面能力的不断提升。在过去十年中,众多非线性光学显微镜的发展在基础研究以及极具潜力的非侵入性诊断工具的开发方面都带来了新的前景。与传统线性显微镜相比,这些技术在穿透深度、空间分辨率、三维光学切片以及较低的光漂白方面具有很大优势。此外,其中一些技术提供了直接在活细胞中光学探测生物学功能的机会,例如,二次谐波产生在可兴奋细胞中用于电势和活性的光学测量就突出了这一点。与成像技术并行,非线性显微镜已发展成为细胞内结构选择性破坏和操纵的新领域,为细胞生物学研究提供了极为有用的工具。在本综述中,我们介绍了非线性显微镜在成像和操纵方面的一些基本特征,并展示了一些示例来说明这些新方法所具有的优势。