[Development of Two-Photon Super-Resolution Microscopy].

Q3 Medicine
Motosuke Tsutsumi, Hirokazu Ishii, Tomomi Nemoto
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引用次数: 0

Abstract

Two-photon excitation microscopy enables in vivo deep-tissue imaging within organisms. This technique is based on two-photon excitation, a nonlinear optical process that uses near-infrared light for excitation, resulting in high tissue permeability. Notably, two-photon excitation occurs only near the focal plane; therefore, minimally invasive tomographic images can be obtained. Owing to these features, two-photon excitation microscopy is currently widely used in medical and life-science research, particularly in the domain of neuroscience for in vivo visualization of deep tissues. However, the use of long-wavelength excitation light in two-photon excitation microscopy has resulted in a larger focused spot size and relatively low spatial resolution, which is a limitation of this technique for further applications. Recent studies have described super-resolution microscopy techniques applied to two-photon excitation microscopy in an attempt to observe living organisms "as they are in their natural state" with high spatial resolution. We have also addressed this topic using an optical approach (two-photon stimulated emission depletion microscopy) and an image analysis approach (two-photon super-resolution radial fluctuation). Here, we describe these approaches together with a discussion of our recent accomplishments.

[双光子超分辨率显微镜的发展]。
双光子激发显微镜可对生物体内的深层组织进行活体成像。这种技术基于双光子激发,这是一种非线性光学过程,使用近红外线进行激发,从而产生高组织渗透性。值得注意的是,双光子激发只发生在焦平面附近,因此可以获得微创断层图像。由于这些特点,双光子激发显微镜目前广泛应用于医学和生命科学研究,特别是神经科学领域的深部组织活体可视化。然而,双光子激发显微镜使用长波长激发光,导致聚焦光斑尺寸较大,空间分辨率相对较低,这限制了该技术的进一步应用。最近的研究描述了应用于双光子激发显微镜的超分辨率显微技术,试图以高空间分辨率观察生物体的 "自然状态"。我们还利用光学方法(双光子激发发射耗损显微镜)和图像分析方法(双光子超分辨率径向波动)解决了这一课题。在此,我们将介绍这些方法,并讨论我们最近取得的成就。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain and Nerve
Brain and Nerve Medicine-Neurology (clinical)
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