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傅里叶变换红外光谱成像在胶原特征分析及胶质瘤分级中的应用

FTIR spectro-imaging of collagens for characterization and grading of gliomas.

机构信息

Chemistry and Biology of Membranes and Nano-Objects, Université de Bordeaux, CNRS UMR 5248, IPB. Allée de Saint Hillaire, F33600 Pessac, France.

出版信息

Biotechnol Adv. 2012 Nov-Dec;30(6):1432-46. doi: 10.1016/j.biotechadv.2012.03.009. Epub 2012 Mar 30.

Abstract

Collagens are a family of at least 30 protein types organized as networks. They constitute the main support material of cells under the form of extracellular matrix as well as for membranes in vessels, organs, and tissue compartments. Collagen network abnormalities are at the origin of many diseases, including myopathies and fibroses. The characterization of collagens remains an analytical challenge due to the insolubility of these molecules and the difficulty encountered in isolating given types without altering their structure or in maintaining network organization, which is critical to diagnosing related pathologies. We have proposed using a vibrational spectroscopy based imaging technique, namely Fourier-transform infrared (FTIR) imaging, for a spatially-resolved analysis of secondary structure of different collagen types in complex samples, and more specifically for characterizing gliomas. With newly developed spectral data treatments and chemometrics using secondary structure parameters of collagen proteins, FTIR imaging is now able to distinguish between several types. On this basis, gliomas have been investigated as specific collagen-rich tissues developing in a non-collagenous environment, providing high specificity to this FTIR imaging utilization. Here, we review the recent advances in this imaging approach for understanding glioma development, with FTIR imaging now being proposed as a molecular histopathology tool for clinicians.

摘要

胶原是至少 30 种蛋白质类型的家族,组织成网络。它们以细胞外基质的形式构成细胞的主要支撑材料,以及血管、器官和组织隔室中的膜。胶原网络异常是许多疾病的根源,包括肌肉疾病和纤维症。由于这些分子的不溶性以及在不改变其结构或维持网络组织的情况下分离给定类型的困难,胶原的表征仍然是一个分析挑战,而网络组织对于诊断相关病理至关重要。我们提出使用基于振动光谱的成像技术,即傅里叶变换红外(FTIR)成像,对复杂样品中不同胶原类型的二级结构进行空间分辨分析,更具体地说是用于表征神经胶质瘤。通过使用胶原蛋白质二级结构参数的新开发的光谱数据处理和化学计量学,FTIR 成像现在能够区分几种类型。在此基础上,神经胶质瘤被研究为在非胶原环境中发展的特定富含胶原的组织,为这种 FTIR 成像的利用提供了高度的特异性。在这里,我们回顾了这种成像方法在理解神经胶质瘤发展方面的最新进展,现在 FTIR 成像被提议作为临床医生的分子组织病理学工具。

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