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用于对I型和II型胶原凝胶进行成像并进行像素分辨率分析的双液相PSHG显微镜。

Dual-LC PSHG microscopy for imaging collagen type I and type II gels with pixel-resolution analysis.

作者信息

Chen Chung-Hwan, Nair Anupama Venugopalan, Chuang Shu-Chun, Lin Yi-Shan, Cheng Mei-Hsin, Lin Chun-Yu, Chang Chia-Ying, Chen Shean-Jen, Lien Chi-Hsiang

机构信息

Orthopaedic Research Centre, Kaohsiung Medical University, Kaohsiung, Taiwan.

Regeneration Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Biomed Opt Express. 2021 Apr 30;12(5):3050-3065. doi: 10.1364/BOE.416193. eCollection 2021 May 1.

Abstract

Collagen of type I (Col I) and type II (Col II) are critical for cartilage and connective tissues in the human body, and several diseases may alter their properties. Assessing the identification and quantification of fibrillar collagen without biomarkers is a challenge. Advancements in non-invasive polarization-resolved second-harmonic generation (PSHG) microscopy have provided a method for the non-destructive investigation of collagen molecular level properties. Here we explored an alternative polarization modulated approach, dual-LC PSHG, that is based on two liquid crystal devices (Liquid crystal polarization rotators, LPRs) operating simultaneously with a laser scanning SHG microscope. We demonstrated that this more accessible technology allows the quick and accurate generation of any desired linear and circular polarization state without any mechanical parts. This study demonstrates that this method can aid in improving the ability to quantify the characteristics of both types of collagen, including pitch angle, anisotropy, and circular dichroism analysis. Using this approach, we estimated the effective pitch angle for Col I and Col II to be 49.7° and 51.6°, respectively. The effective peptide pitch angle for Col II gel was first estimated and is similar to the value obtained for Col I gel in the previous studies. Additionally, the difference of the anisotropy parameter of both collagen type gels was assessed to be 0.293, which reflects the different type molecular fibril assembly. Further, our work suggests a potential method for monitoring and differentiating different collagen types in biological tissues, especially cartilage or connective tissue.

摘要

I型胶原蛋白(Col I)和II型胶原蛋白(Col II)对人体中的软骨和结缔组织至关重要,一些疾病可能会改变它们的特性。在没有生物标志物的情况下评估纤维状胶原蛋白的识别和定量是一项挑战。非侵入性偏振分辨二次谐波产生(PSHG)显微镜技术的进步为胶原蛋白分子水平特性的无损研究提供了一种方法。在这里,我们探索了一种基于两个液晶装置(液晶偏振旋转器,LPR)与激光扫描SHG显微镜同时运行的替代偏振调制方法——双LC PSHG。我们证明,这种更容易获得的技术可以在没有任何机械部件的情况下快速准确地产生任何所需的线性和圆偏振态。这项研究表明,该方法有助于提高定量两种胶原蛋白特性的能力,包括螺距角、各向异性和圆二色性分析。使用这种方法,我们估计Col I和Col II的有效螺距角分别为49.7°和51.6°。首次估计了Col II凝胶的有效肽螺距角,其与先前研究中Col I凝胶获得的值相似。此外,两种胶原蛋白类型凝胶的各向异性参数差异评估为0.293,这反映了不同类型分子原纤维的组装情况。此外,我们的工作提出了一种监测和区分生物组织中不同类型胶原蛋白的潜在方法,尤其是软骨或结缔组织。

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