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Multimodal imaging quality control of epithelia regenerated with cultured human donor corneal limbal epithelial stem cells

机译:培养的人类供体角膜缘角膜缘上皮干细胞再生的上皮细胞的多模式成像质量控制

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摘要

Current imaging techniques for the characterization of differentiated corneal limbal stem cells are destructive and cannot be used in eye bank for monitoring the regenerated epithelium in culture. We presented a minimally invasive, multimodal, marker-free imaging method for the investigation of epithelia regenerated with cultured human donor corneal limbal epithelial stem cells. Two-photon fluorescence and harmonic generation signals were collected from specimens in culture and used for evaluating the structure and morphology of epithelia cultured on two different bio-scaffolds; in addition, donor human corneal tissues were used as controls. The method provided reliable information on the organization of cellular and extracellular components of biomaterial substrates and was highly sensitive to determine differences between the density packing arrangement of epithelial cells of different biomaterials without relying on inferences from exogenous labels. The present minimally invasive standardized quality control methodology can be reliably translated to eye banks and used for monitoring harvested corneal limbal stem cells growth and differentiation in bioengineered materials.
机译:当前表征分化的角膜缘干细胞的成像技术具有破坏性,不能在眼库中用于监测培养物中的再生上皮。我们提出了一种微创,多模式,无标记的成像方法,用于研究培养的人供体角膜缘角膜缘上皮干细胞再生的上皮细胞。从培养的标本中收集双光子荧光和谐波产生信号,并用于评估在两种不同生物支架上培养的上皮细胞的结构和形态。另外,将供体人角膜组织用作对照。该方法提供了有关生物材料底物的细胞和细胞外成分组织的可靠信息,并且高度敏感地确定了不同生物材料上皮细胞的密度堆积排列之间的差异,而无需依赖于外源标记的推断。当前的微创标准化质量控制方法可以可靠地转化为眼库,并用于监测生物工程材料中角膜缘干细胞的生长和分化。

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