首页> 外文会议>Conference on Imaging, Manipulation, and Analysis of Biomolecules, Cell, and Tissues; 20080121-23; San Jose,CA(US) >Characterization of dermal structural assembly in normal and pathological connective tissues by intrinsic signal multiphoton optical microscopy
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Characterization of dermal structural assembly in normal and pathological connective tissues by intrinsic signal multiphoton optical microscopy

机译:通过固有信号多光子光学显微镜表征正常和病理结缔组织中的真皮结构组件

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摘要

Employing a reflectance multi-photon microscopy (MPM) technique, we developed novel method to quantitatively study the three-dimensional assembly of structural proteins within bulk of dermal ECMs. Using a structurally simplified model of skin with enzymatically dissected epidermis, we find that low resolution MPM clearly discriminates between normal and pathological dermis. High-resolution images revealed that the backscattered MPM signals are affected by the assembly of collagen fibrils and fibers within this system. Exposure of tissues to high concentrations of potentially denaturing chemicals also resulted in the reduction of SHG signals from structural proteins which coincided with the appearance of aggregated fluorescent structures.
机译:利用反射多光子显微镜(MPM)技术,我们开发了新颖的方法来定量研究大量皮肤ECM中结构蛋白的三维组装。使用具有酶切表皮的皮肤的结构简化模型,我们发现低分辨率MPM可以清楚地区分正常真皮和病理真皮。高分辨率图像显示,反向散射的MPM信号受该系统中胶原蛋白原纤维和纤维的组装影响。将组织暴露于高浓度的可能会导致变性的化学物质中,还导致结构蛋白的SHG信号减少,这与聚集的荧光结构相吻合。

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