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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Epithelial basement membrane of human decellularized cornea as a suitable substrate for differentiation of embryonic stem cells into corneal epithelial-like cells
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Epithelial basement membrane of human decellularized cornea as a suitable substrate for differentiation of embryonic stem cells into corneal epithelial-like cells

机译:人脱细胞基角膜的上皮基底膜作为合适的基质,用于将胚胎干细胞分化到角膜上皮样细胞中

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摘要

The ability to decellularize and recellularize the corneas deemed unsuitable for transplantation may increase the number of available grafts. Decellularized corneas (DCs) may provide a natural microenvironment for cell adhesion and differentiation. Despite this, no study to date has evaluated their efficacy as a substrate for the induction of stem cell differentiation into corneal cells. The present study aimed to compare the efficiency of NaCl and NaCl plus nucleases methods to decellularize whole human corneas, and to investigate the effect of epithelial basement membrane (EBM) of whole DCs on the ability of human embryonic stem cells (hESCs) to differentiate into corneal epithelial-like cells when cultured in animal serum-free differentiation medium. As laminin is the major component of EBM, we also investigated its effect on hESCs differentiation. The decellularization efficiency and integrity of the extracellular matrix (ECM) obtained were investigated by histology, electron microscopy, DNA quantification, immunofluorescence, and nuclear staining. The ability of hESCs to differentiate into corneal epithelial-like cells when seeded on the EBM of DCs or laminin-coated wells was evaluated by immunofluorescence and RT-qPCR analyses. NaCl treatment alone, without nucleases, was insufficient to remove cellular components, while NaCl plus nucleases treatment resulted in efficient decellularization and preservation of the ECM. Unlike cells induced to differentiate on laminin, hESCs differentiated on DCs expressed high levels of corneal epithelial-specific markers, keratin 3 and keratin 12. It was demonstrated for the first time that the decellularized matrices had a positive effect on the differentiation of hESCs towards corneal epithelial-like cells. Such a strategy supports the potential applications of human DCs and hESCs in corneal epithelium tissue engineering.
机译:认为不适合移植的角膜的脱叶和透彻的能力可能增加可用移植物的数量。瞳孔化玉米体(DCS)可以提供用于细胞粘附和分化的天然微环境。尽管如此,迄今尚无研究已经评估了它们作为诱导干细胞分化成角膜细胞的基质的功效。本研究旨在比较NaCl和NaCl Plus核酸酶方法的效率,以脱节整个人类角膜,并探讨整个DC对人胚胎干细胞(HESC)分化的能力的上皮基底膜(EBM)的效果在无血清分化培养基中培养时角膜上皮样细胞。由于薄膜是EBM的主要成分,我们还研究了对HESCS分化的影响。通过组织学,电子显微镜,DNA定量,免疫荧光和核染色研究了所得细胞外基质(ECM)的脱细胞化效率和完整性。通过免疫荧光和RT-QPCR分析评估当在DCS或层粘连蛋白涂覆孔的eBM上接种时,HECS将HESC分化成角膜上皮细胞的能力。单独的NaCl处理,没有核酸酶,不足以去除细胞组分,而NaCl加上核酸酶处理导致ECM的有效脱细胞化和保存。与所诱导的细胞不同,在层蛋白上区分,DCS的HESC表达了高水平的角膜上皮特异性标记,角膜素3和角蛋白12.首次证明了脱细胞的基质对HESCS对角膜的阳性作用进行了积极影响上皮细胞。这种策略支持人类DC和HESC在角膜上皮组织工程中的潜在应用。

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