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Wavelength-Dependent Second Harmonic Generation Circular Dichroism for Differentiation of Col I and Col III Isoforms in Stromal Models of Ovarian Cancer Based on Intrinsic Chirality Differences

机译:基于内在手性差异的波长依赖性第二谐波生成圆二色性用于区分卵巢癌基质模型中的Col I和Col III亚型

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摘要

Extensive remodeling of the extracellular matrix (ECM) occurs in many epithelial cancers. For example, in ovarian cancer, upregulation of collagen isoform type III has been linked to invasive forms of the disease, and this change may be a potential biomarker. To examine this possibility, we implemented wavelength-dependent second harmonic generation circular dichroism (SHG-CD) imaging microscopy to quantitatively determine changes in chirality in ECM models comprised of different Col I/Col III composition. In these models, Col III was varied between 0 and 40%, and we found increasing Col III results in reduced net chirality, consistent with structural biology studies of Col I and III in tissues where the isoforms comingle in the same fibrils. We further examined the wavelength dependence of the SHG-CD to both optimize the response and gain insight into the underlying mechanism. We found using shorter SHG excitation wavelengths resulted in increased SHG-CD sensitivity, where this is consistent with the electric-dipole-coupled oscillator model suggested previously for the nonlinear chirality response from thin films. Moreover, the sensitivity is further consistent with the wavelength dependency of SHG intensity fit to a two-state model of the two-photon absorption in collagen. We also provide experimental calibration protocols to implement the SHG-CD modality on a laser scanning microscope. We last suggest that the technique has broad applicability in probing a wide range of diseased states with changes in collagen molecular structure.
机译:细胞外基质(ECM)的广泛重塑发生在许多上皮癌中。例如,在卵巢癌中,III型胶原同工型的上调与该疾病的侵袭性形式有关,这种变化可能是潜在的生物标志物。为了检验这种可能性,我们实施了依赖于波长的二次谐波生成圆二色性(SHG-CD)成像显微镜,以定量确定由不同Col I / Col III组成的ECM模型中手性的变化。在这些模型中,Col III在0%到40%之间变化,并且我们发现增加的Col III结果会降低净手性,这与同工型在相同原纤维中融合的组织中Col I和III的结构生物学研究一致。我们进一步检查了SHG-CD的波长依赖性,以优化响应并深入了解其潜在机理。我们发现使用较短的SHG激发波长会导致SHG-CD灵敏度提高,这与先前针对薄膜的非线性手性响应所建议的电偶极耦合振荡器模型是一致的。此外,敏感性进一步与SHG强度的波长依赖性一致,所述SHG强度适合于胶原中的双光子吸收的二态模型。我们还提供实验校准协议,以在激光扫描显微镜上实现SHG-CD模式。我们最后提出,该技术在探测胶原蛋白分子结构变化的多种疾病状态方面具有广泛的适用性。

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  • 期刊名称 other
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  • 年(卷),期 -1(121),8
  • 年度 -1
  • 页码 1749–1757
  • 总页数 22
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