Walter-Brendel-Zentrum für Experimentelle Medizin, Ludwig-Maximilians-Universität München, München, Germany.
PLoS One. 2011;6(11):e28237. doi: 10.1371/journal.pone.0028237. Epub 2011 Nov 28.
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.
二次谐波产生(SHG)和三次谐波产生(THG)显微镜基于光学效应,这些光学效应是由样品的特定固有物理性质引起的。作为一种多光子激光扫描方法,它不基于荧光,结合了非标记技术的优点和信号产生局限于焦平面的优点,从而允许对组织内几百微米深的无焦背景的高分辨率 3D 图像体积进行重建。虽然在哺乳动物软组织中,SHG 主要局限于胶原蛋白纤维和横纹肌肌球蛋白,但 THG 可以在各种结构中产生,因为它是在激发激光的焦体积内的折射率变化等界面处产生的。此外,像血红蛋白这样的着色剂可以引起共振增强,从而产生强烈的 THG 信号。我们将 SHG 和 THG 显微镜应用于鼠(Mus musculus)肌肉,这是一种用于生理研究的成熟模型系统,以研究它们在非标记组织成像中的潜力。除了胶原蛋白纤维和肌纤维亚结构外,THG 还使我们能够可视化血管壁和红细胞以及附着在血管壁上、位于血管外组织中或穿过血管外组织的白细胞。此外,还可以清楚地识别周围神经纤维。3D 显示的结构甚至可以达到核染色质分布的细节,比明场显微镜所能获得的更为详细。据我们所知,这些物体中的大多数以前没有通过 THG 或任何非标记 3D 方法进行过可视化。THG 允许进行非标记显微镜检查,具有固有光学切片功能,因此与明场显微镜相比可能具有类似的改进,与传统荧光显微镜相比,共聚焦激光扫描显微镜也具有类似的改进。