Schenke-Layland Katja
Cardiovascular Research Laboratory, David Geffen School of Medicine, University of California, Los Angeles, UCLA, 675 Charles E. Young Drive South, MRL 3-579, Los Angeles, CA 90095, USA.
J Biophotonics. 2008 Dec;1(6):451-62. doi: 10.1002/jbio.200810045.
Multiphoton microscopy has become a powerful method for the artifact-free, nondestructive evaluation of deep-tissue cells and extracellular matrix (ECM) structures in their native environment. By interacting with highly non-centrosymmetric molecular assemblies such as fibrillar collagen, the non-linear process called second harmonic generation (SHG) has also proven to be an important diagnostic tool for the visualization of ECM compartments in situ with submicron resolution without the need for tissue processing. This review reports on applications of multiphoton-induced autofluorescence and SHG microscopy to identify collagen and elastic fiber orientation in native, tissue-engineered and processed, as well as healthy and diseased, tissues and organs. SHG signal profiling was used to quantify ECM damage in various cardiovascular and exocrine tissues, as well as cartilage. These novel imaging modalities open the general possibility of high-resolution in situ and more important in vivo imaging of ECM structures, cells and intracellular organelles in living intact tissues.
多光子显微镜已成为一种强大的方法,可在自然环境中对深层组织细胞和细胞外基质(ECM)结构进行无伪像、非破坏性评估。通过与高度非中心对称的分子组装体(如纤维状胶原蛋白)相互作用,称为二次谐波产生(SHG)的非线性过程也已被证明是一种重要的诊断工具,可在无需组织处理的情况下以亚微米分辨率原位可视化ECM区室。本综述报道了多光子诱导的自发荧光和SHG显微镜在识别天然、组织工程化和经处理的以及健康和患病的组织和器官中的胶原蛋白和弹性纤维取向方面的应用。SHG信号分析被用于量化各种心血管和外分泌组织以及软骨中的ECM损伤。这些新颖的成像方式为在完整的活体组织中原位进行高分辨率成像以及更重要的在体内对ECM结构、细胞和细胞内细胞器进行成像提供了普遍可能性。