首页> 外文期刊>Tissue engineering, Part C. Methods >Raman microspectroscopy: a noninvasive analysis tool for monitoring of collagen-containing extracellular matrix formation in a medium-throughput culture system.
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Raman microspectroscopy: a noninvasive analysis tool for monitoring of collagen-containing extracellular matrix formation in a medium-throughput culture system.

机译:拉曼光谱:一种无创分析工具,用于监测中通量培养系统中含胶原的细胞外基质的形成。

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摘要

The three-dimensional environment is known to play an important role in promoting cell-matrix interactions. We have investigated the possibility of using Raman microspectroscopy--which has the great advantage of noninvasive sensing--for in vitro monitoring of extracellular matrix (ECM) formation in a medium-throughput pellet (3D) culture system with soft-litography, agarose-microwell arrays. Chondrocytes were seeded in the agarose microwells in basic or chondrocyte medium. After 3, 7, and 14 days of culture, samples were analyzed for ECM formation by Raman microspectroscopy, histology, and immunofluorescence. ECM formation in the chondrocyte medium-cultured samples was detected by histology and immunofluorescence, and also noninvasively by Raman microspectroscopy. The Raman band of collagen found at 937 cm(-1) can be used as a Raman marker for collagen-containing ECM formation over time in the chondrocyte pellets. This culture system can be implemented as a medium-throughput platform for Raman applications and screening microtissue formation, since with these agarose-microwell arrays relatively large numbers of cell pellets could be screened in a short time in situ, without having to transfer the pellets onto microscopic slides. Moreover, in this manner the culture system is suitable for long-term, real-time live-cell measurements.
机译:众所周知,三维环境在促进细胞-基质相互作用中起着重要作用。我们已经研究了使用拉曼显微技术(具有无创传感技术的巨大优势)在中通量沉淀(3D)培养系统中通过软光刻,琼脂糖-微孔阵列。将软骨细胞接种在碱性或软骨细胞培养基中的琼脂糖微孔中。培养3、7和14天后,通过拉曼光谱,组织学和免疫荧光分析样品的ECM形成。通过组织学和免疫荧光检测软骨细胞培养基培养样品中的ECM形成,并且通过拉曼光谱法无创地检测。在937 cm(-1)处发现的胶原蛋白拉曼光谱带可用作软骨细胞沉淀中随着时间推移含胶原蛋白ECM形成的拉曼标记。该培养系统可以实现为拉曼应用和筛选微组织形成的中等通量平台,因为使用这些琼脂糖微孔阵列可以在短时间内原位筛选相对大量的细胞沉淀,而无需将沉淀转移到微观幻灯片。而且,以这种方式,培养系统适合于长期,实时的活细胞测量。

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