Uckermann Ortrud, Galli Roberta, Leupold Susann, Coras Roland, Meinhardt Matthias, Hallmeyer-Elgner Susanne, Mayer Thomas, Storch Alexander, Schackert Gabriele, Koch Edmund, Blümcke Ingmar, Steiner Gerald, Kirsch Matthias
Neurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Clinical Sensoring and Monitoring, Clinic of Anesthesiology and Intensive Care Therapy, Medical Faculty, TU Dresden, Dresden, Germany.
Epilepsia. 2017 Jan;58(1):e1-e5. doi: 10.1111/epi.13598. Epub 2016 Nov 7.
The properties and structure of tissue can be visualized without labeling or preparation by multiphoton microscopy combining coherent anti-Stokes Raman scattering (CARS), addressing lipid content, second harmonic generation (SHG) showing collagen, and two-photon excited fluorescence (TPEF) of endogenous fluorophores. We compared samples of sclerotic and nonsclerotic human hippocampus to detect pathologic changes in the brain of patients with pharmacoresistant temporomesial epilepsy (n = 15). Multiphoton microscopy of cryosections and bulk tissue revealed hippocampal layering and micromorphologic details in accordance with reference histology: CARS displayed white and gray matter layering and allowed the assessment of axonal myelin. SHG visualized blood vessels based on adventitial collagen. In addition, corpora amylacea (CoA) were found to be SHG-active. Pyramidal cell bodies were characterized by intense cytoplasmic endogenous TPEF. Furthermore, diffuse TPEF around blood vessels was observed that co-localized with positive albumin immunohistochemistry and might indicate degeneration-associated vascular leakage. We present a label-free and fast optical approach that analyzes pathologic aspects of HS. Hippocampal layering, loss of pyramidal cells, and presence of CoA indicative of sclerosis are visualized. Label-free multiphoton microscopy has the potential to extend the histopathologic armamentarium for ex vivo assessment of changes of the hippocampal formation on fresh tissue and prospectively in vivo.
通过结合相干反斯托克斯拉曼散射(CARS,用于检测脂质含量)、二次谐波产生(SHG,显示胶原蛋白)以及内源性荧光团的双光子激发荧光(TPEF)的多光子显微镜技术,无需标记或制备即可可视化组织的特性和结构。我们比较了硬化和非硬化人类海马体样本,以检测药物难治性颞叶内侧癫痫患者(n = 15)大脑中的病理变化。冷冻切片和大块组织的多光子显微镜检查揭示了与参考组织学一致的海马分层和微观形态细节:CARS显示白质和灰质分层,并允许评估轴突髓鞘。SHG基于外膜胶原蛋白使血管可视化。此外,发现淀粉样体(CoA)具有SHG活性。锥体细胞体的特征是强烈的细胞质内源性TPEF。此外,观察到血管周围弥漫性TPEF,其与白蛋白免疫组化阳性共定位,可能表明与变性相关的血管渗漏。我们提出了一种无标记且快速的光学方法来分析海马硬化的病理方面。可视化了海马分层、锥体细胞丢失以及指示硬化的CoA的存在。无标记多光子显微镜有潜力扩展组织病理学手段,用于对新鲜组织和前瞻性体内海马结构变化的离体评估。