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Label-Free 3D Visualization of Cellular and Tissue Structures in Intact Muscle with Second and Third Harmonic Generation Microscopy

机译:使用第二代和第三代谐波显微镜观察完整肌肉中细胞和组织结构的无标签3D可视化

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摘要

Second and Third Harmonic Generation (SHG and THG) microscopy is based on optical effects which are induced by specific inherent physical properties of a specimen. As a multi-photon laser scanning approach which is not based on fluorescence it combines the advantages of a label-free technique with restriction of signal generation to the focal plane, thus allowing high resolution 3D reconstruction of image volumes without out-of-focus background several hundred micrometers deep into the tissue. While in mammalian soft tissues SHG is mostly restricted to collagen fibers and striated muscle myosin, THG is induced at a large variety of structures, since it is generated at interfaces such as refraction index changes within the focal volume of the excitation laser. Besides, colorants such as hemoglobin can cause resonance enhancement, leading to intense THG signals. We applied SHG and THG microscopy to murine (Mus musculus) muscles, an established model system for physiological research, to investigate their potential for label-free tissue imaging. In addition to collagen fibers and muscle fiber substructure, THG allowed us to visualize blood vessel walls and erythrocytes as well as white blood cells adhering to vessel walls, residing in or moving through the extravascular tissue. Moreover peripheral nerve fibers could be clearly identified. Structure down to the nuclear chromatin distribution was visualized in 3D and with more detail than obtainable by bright field microscopy. To our knowledge, most of these objects have not been visualized previously by THG or any label-free 3D approach. THG allows label-free microscopy with inherent optical sectioning and therefore may offer similar improvements compared to bright field microscopy as does confocal laser scanning microscopy compared to conventional fluorescence microscopy.
机译:第二和第三谐波产生(SHG和THG)显微镜基于光学效应,该效应是由样品的特定固有物理特性引起的。作为一种不基于荧光的多光子激光扫描方法,它结合了无标记技术的优点以及对焦平面信号产生的限制,因此可以在没有离焦背景的情况下实现图像体积的高分辨率3D重建深入组织数百微米。在哺乳动物软组织中,SHG主要限于胶原纤维和横纹肌肌球蛋白,而THG则在多种结构中被诱导,因为THG是在激发激光焦距内的折射率变化等界面处产生的。此外,诸如血红蛋白之类的着色剂可引起共振增强,导致强烈的THG信号。我们将SHG和THG显微镜应用于鼠(鼠肌肉)肌肉(已建立的生理研究模型系统),以研究它们在无标签组织成像中的潜力。除了胶原纤维和肌肉纤维的子结构,THG还使我们能够观察到血管壁和红细胞以及粘附在血管壁上,驻留在血管外组织或在血管外组织中移动的白细胞。此外,可以清楚地识别周围神经纤维。直至核染色质分布的结构均以3D形式显示,并且比通过明场显微镜可获得的细节更为详细。据我们所知,大多数这些对象以前尚未通过THG或任何无标签的3D方法进行可视化。 THG允许无标记的显微镜具有固有的光学切片,因此与明场显微镜相比,共焦激光扫描显微镜与常规荧光显微镜相比,可以提供类似的改进。

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