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Characterization of Cholesterol Crystals in Atherosclerotic Plaques Using Stimulated Raman Scattering and Second-Harmonic Generation Microscopy

机译:刺激拉曼散射和二次谐波产生显微镜表征动脉粥样硬化斑块中的胆固醇晶体。

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摘要

Cholesterol crystals (ChCs) have been identified as a major factor of plaque vulnerability and as a potential biomarker for atherosclerosis. Yet, due to the technical challenge of selectively detecting cholesterol in its native tissue environment, the physiochemical role of ChCs in atherosclerotic progression remains largely unknown. In this work, we demonstrate the utility of hyperspectral stimulated Raman scattering (SRS) microscopy combined with second-harmonic generation (SHG) microscopy to selectively detect ChC. We show that despite the polarization sensitivity of the ChC Raman spectrum, cholesterol monohydrate crystals can be reliably discriminated from aliphatic lipids, from structural proteins of the tissue matrix and from other condensed structures, including cholesteryl esters. We also show that ChCs exhibit a nonvanishing SHG signal, corroborating the noncentrosymmetry of the crystal lattice composed of chiral cholesterol molecules. However, combined hyperspectral SRS and SHG imaging reveals that not all SHG-active structures with solidlike morphologies can be assigned to ChCs. This study exemplifies the merit of combining SRS and SHG microscopy for an enhanced label-free chemical analysis of crystallized structures in diseased tissue.
机译:胆固醇晶体(ChCs)已被确定为斑块易损性的主要因素,并且是动脉粥样硬化的潜在生物标记。然而,由于在其天然组织环境中选择性检测胆固醇的技术挑战,ChCs在动脉粥样硬化进展中的生理化学作用仍然未知。在这项工作中,我们证明了高光谱激发拉曼散射(SRS)显微镜与二次谐波产生(SHG)显微镜相结合以选择性检测ChC的实用性。我们显示,尽管ChC拉曼光谱具有偏振敏感性,但胆固醇一水合物晶体可以可靠地与脂肪族脂质,组织基质的结构蛋白以及包括胆固醇酯在内的其他缩合结构区分开。我们还显示ChCs展现出不消失的SHG信号,证实了由手性胆固醇分子组成的晶格的非中心对称性。但是,组合的高光谱SRS和SHG成像显示,并非所有具有固体形态的SHG活性结构都可以分配给ChC。这项研究例证了结合SRS和SHG显微镜对病变组织中结晶结构进行增强的无标记化学分析的优点。

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