Undergrowth Collagen Fibers Analysis by Fingerprint Enhancement Method

IF 2.4 4区 生物学 Q4 CELL BIOLOGY
Clara Manesco, Thierry Cloitre, Marta Martin, Yannick Nicolas Gerber, Florence Evelyne Perrin, Oscar Saavedra-Villanueva, Csilla Gergely
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引用次数: 0

Abstract

Collagen is a key protein in mammals that maintains structural integrity within tissues. A failure in fibrillar collagen reorganization can induce cancer or fibrosis formation, such as in spinal cord injury (SCI), where the healing process after the initial trauma leads to the formation of scar tissue, which includes fibrosis. As there is no current treatment targeting the fibrotic process directly, a better understanding of collagen properties can thus help to apprehend malignant states.

Characterization of collagen fibers has been widely explored on second-harmonic generation (SHG) images, due to the label-free nature of the SHG imaging technique. It has been performed with various fibers extraction methods such as curvelet transform (CT) implemented in the open-source software CurveAlign. However, when it comes to investigating undergrowth collagen fibers (collagen fibers that are still under reorganization) as observed in SCI, the CT method becomes complex to tune for nonadvanced users in order to properly segment the fibers. To improve collagen detection in the case of undergrowth fibers, we propose a methodology based on the fingerprint enhancement (FP-E) algorithm that requires fewer user input parameters and is less time-consuming. Our method was extensively tested on SHG data from injured spinal cord samples.

We obtained metrics that depicted changes in collagen organization over time, particularly a significant increase in fiber density, demonstrating the FP-E algorithm was properly adapted to address the evolution of collagen properties after SCI. Besides the simpler tuning of the method compared to commonly used software, the combination with further characterization of the extracted fibers could lead to consider fibrillar collagen as a biomarker in diseases where fibers are under development. The FP-E algorithm is provided in the article.

Abstract Image

胶原蛋白是哺乳动物体内维持组织结构完整性的关键蛋白质。纤维胶原重组失败会诱发癌症或纤维化的形成,例如在脊髓损伤(SCI)中,最初创伤后的愈合过程会导致瘢痕组织的形成,其中包括纤维化。由于目前还没有直接针对纤维化过程的治疗方法,因此更好地了解胶原蛋白的特性有助于了解恶性状态。由于二次谐波发生(SHG)成像技术的无标记性,胶原蛋白纤维的表征已在二次谐波发生(SHG)图像上得到广泛探索。在二次谐波发生(SHG)图像上对胶原纤维的表征已被广泛探索,这是因为二次谐波发生(SHG)成像技术具有无标记的特性。然而,在研究 SCI 中观察到的生长不足的胶原纤维(仍在重组中的胶原纤维)时,CT 方法对于非高级用户来说变得复杂,难以调整以正确分割纤维。为了改进生长不足纤维情况下的胶原蛋白检测,我们提出了一种基于指纹增强(FP-E)算法的方法,该算法需要的用户输入参数更少,耗时更短。我们获得的指标描述了胶原组织随时间的变化,尤其是纤维密度的显著增加,这表明 FP-E 算法经过了适当调整,可以应对 SCI 后胶原特性的演变。与常用软件相比,该方法的调整更为简单,此外,结合对提取纤维的进一步表征,可将纤维胶原蛋白视为纤维正在发育的疾病的生物标志物。文章中提供了 FP-E 算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biology of the Cell
Biology of the Cell 生物-细胞生物学
CiteScore
5.30
自引率
0.00%
发文量
53
审稿时长
>12 weeks
期刊介绍: The journal publishes original research articles and reviews on all aspects of cellular, molecular and structural biology, developmental biology, cell physiology and evolution. It will publish articles or reviews contributing to the understanding of the elementary biochemical and biophysical principles of live matter organization from the molecular, cellular and tissues scales and organisms. This includes contributions directed towards understanding biochemical and biophysical mechanisms, structure-function relationships with respect to basic cell and tissue functions, development, development/evolution relationship, morphogenesis, stem cell biology, cell biology of disease, plant cell biology, as well as contributions directed toward understanding integrated processes at the organelles, cell and tissue levels. Contributions using approaches such as high resolution imaging, live imaging, quantitative cell biology and integrated biology; as well as those using innovative genetic and epigenetic technologies, ex-vivo tissue engineering, cellular, tissue and integrated functional analysis, and quantitative biology and modeling to demonstrate original biological principles are encouraged.
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