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用于细胞外基质沉积无创成像的细胞胶原蛋白生成的荧光标记

Fluorescent Labeling of Collagen Production by Cells for Noninvasive Imaging of Extracellular Matrix Deposition.

作者信息

Bardsley Katie, Yang Ying, El Haj Alicia J

机构信息

Institute of Science and Technology in Medicine, School of Medicine, Keele University , Stoke-on-Trent, United Kingdom .

出版信息

Tissue Eng Part C Methods. 2017 Apr;23(4):228-236. doi: 10.1089/ten.tec.2017.0008. Epub 2017 Mar 24.

DOI:10.1089/ten.tec.2017.0008
PMID:28338443
Abstract

Extracellular matrix (ECM) is an essential component of tissues and provides both integrity and biological cues for cells. Collagen is one of the major proteins found within the ECM and therefore is an essential component of all engineered tissues. Therefore, in this article, we present a method for the online real-time monitoring of collagen deposition in three-dimensional engineered constructs. This method revolves around modification of collagen through the addition of azide-L-proline to cell culture media. The incorporation of azide-L-proline into the neocollagen produced by cells can then be detected by reaction with 10 mM of a Click-IT Alexa Fluor 488 DIBO Alkyne. The reaction was shown as being specific to the collagen as little background staining was observed in cultures, which did not contain the modified proline, and the staining was also depleted after treatment with collagenase and colocalization of collagen type I staining by immunochemistry assay. Real-time online staining of collagen deposition was observed under different culture conditions without affecting proliferation. Collagen deposition was observed to be increased under mechanical stimulation; however, the localization varied across stimulation regimes. This is a new technique for real-time monitoring of cell-produced collagen and will be a valuable addition to the tissue engineering field.

摘要

细胞外基质(ECM)是组织的重要组成部分,为细胞提供完整性和生物信号。胶原蛋白是细胞外基质中发现的主要蛋白质之一,因此是所有工程组织的重要组成部分。因此,在本文中,我们提出了一种在三维工程构建体中在线实时监测胶原蛋白沉积的方法。该方法围绕通过向细胞培养基中添加叠氮基-L-脯氨酸来修饰胶原蛋白展开。然后,通过与10 mM的Click-IT Alexa Fluor 488 DIBO炔烃反应,可以检测到叠氮基-L-脯氨酸掺入细胞产生的新胶原蛋白中。该反应显示对胶原蛋白具有特异性,因为在不含修饰脯氨酸的培养物中观察到很少的背景染色,并且在用胶原酶处理后染色也消失,并且通过免疫化学分析观察到I型胶原蛋白染色的共定位。在不影响增殖的不同培养条件下观察到胶原蛋白沉积的实时在线染色。在机械刺激下观察到胶原蛋白沉积增加;然而,其定位在不同的刺激方案中有所不同。这是一种实时监测细胞产生的胶原蛋白的新技术,将为组织工程领域增添宝贵的内容。

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