利用无标记中红外光声显微镜对脂肪组织炎症进行快速组织学评估

Vito Ko, Marie C. Goess, Lukas Scheel-Platz, Tao Yuan, Andriy Chmyrov, Dominik Jüstel, Jürgen Ruland, Vasilis Ntziachristos, Selina J. Keppler, Miguel A. Pleitez
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摘要

传统的组织学以及免疫组织化学或免疫荧光技术可精确地研究组织炎症过程中的形态和表型变化。然而,尽管这些技术具有高度特异性,但需要多个耗时的步骤来应用外源标签,这可能会导致形态偏离原生组织结构。与这些技术不同,中红外(mid-IR)显微光谱技术是一种无标记光学成像方法,可在不改变样本原生成分的情况下检索内源性生物分子对比度。然而,由于生物组织对水的强烈光学吸收,传统的中红外显微光谱法仅限于干燥的薄组织(5-10 微米)制备,因此,与传统成像技术相比,它还需要耗时的步骤。在这里,作为对未经处理的组织进行无标记分析组织学的一步,我们应用中红外光声显微镜(MiROM)通过振动激发来检索固有的分子对比度,同时克服了传统中红外成像在厚(毫米范围)组织中的水-组织不透明性。在这项概念验证研究中,我们展示了如何应用 MiROM 快速、无标记、无损地评估切除的白色脂肪组织中的炎症特征,即冠状结构的形成和脂肪细胞形态的变化。
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Fast histological assessment of adipose tissue inflammation by label-free mid-infrared optoacoustic microscopy
Conventional histology, as well as immunohistochemistry or immunofluorescence, enables the study of morphological and phenotypical changes during tissue inflammation with single-cell accuracy. However, although highly specific, such techniques require multiple time-consuming steps to apply exogenous labels, which might result in morphological deviations from native tissue structures. Unlike these techniques, mid-infrared (mid-IR) microspectroscopy is a label-free optical imaging method that retrieves endogenous biomolecular contrast without altering the native composition of the samples. Nevertheless, due to the strong optical absorption of water in biological tissues, conventional mid-IR microspectroscopy has been limited to dried thin (5–10 µm) tissue preparations and, thus, it also requires time-consuming steps—comparable to conventional imaging techniques. Here, as a step towards label-free analytical histology of unprocessed tissues, we applied mid-IR optoacoustic microscopy (MiROM) to retrieve intrinsic molecular contrast by vibrational excitation and, simultaneously, to overcome water-tissue opacity of conventional mid-IR imaging in thick (mm range) tissues. In this proof-of-concept study, we demonstrated application of MiROM for the fast, label-free, non-destructive assessment of the hallmarks of inflammation in excised white adipose tissue; i.e., formation of crown-like structures and changes in adipocyte morphology.
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