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首页> 外文期刊>RSC Advances >Detergent-free decellularization of bovine costal cartilage for chondrogenic differentiation of human adipose mesenchymal stem cells in vitro
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Detergent-free decellularization of bovine costal cartilage for chondrogenic differentiation of human adipose mesenchymal stem cells in vitro

机译:牛肋软骨无洗涤剂脱细胞用于人脂肪间充质干细胞体外成软骨分化

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摘要

In this study, we report a novel, detergent-free decellularization protocol for the preparation of intact cartilage ECM-based scaffolds (CEbS) during an effective decalcification process. On treatment with 10 mM Na(2)EDTA, the amount of calcium lost was around 55% +/- 5% (percent +/- S.D.%) (n = 3) and nearly 84% of the nuclear material was removed; however, the most effective removal was observed on treatment with 10 mM Na2EDTA combined with 0.5% Triton X-100 for 48 hours. Notably, our proposed method decreased the GAG content by only 5% compared to untreated CEbS (380.37 +/- 16.02 mu g mg(-1) dry weight). There was no significant difference in hydroxyproline content between the untreated (13.04 +/- 1.51 mg mg(-1) dry weight) sample and our proposed method (12.95 +/- 1.55 mg mg(-1) dry weight). The scaffold morphology and cell attachment were evaluated using SEM micrographs, and the cells that were inoculated with detergent-free decellularized CEbS for 14, 21 and 28 days covered the scaffold area, including the porous cavities. Microscopic observations showed that the cell density increased day by day and there was no cytotoxic evidence for the scaffolds, which is a desirable environment for cells. The histochemical and immunohistochemical assessments are supported by glycosaminoglycan and hydroxyproline assays. The proposed detergent-free decellularization technique could be a promising method for cartilage tissue regeneration.
机译:在这项研究中,我们报告了一种新型的,无洗涤剂的脱细胞方案,用于在有效的脱钙过程中制备完整的基于软骨ECM的支架(CEbS)。用10 mM Na(2)EDTA处理时,钙损失的量约为55%+/- 5%(百分比+/- S.D。%)(n = 3),并且除去了将近84%的核材料。但是,用10 mM Na2EDTA和0.5%Triton X-100混合处理48小时观察到最有效的去除效果。值得注意的是,与未处理的CEbS(380.37 +/- 16.02μg mg(-1)干重)相比,我们提出的方法仅将GAG含量降低了5%。未经处理的(13.04 +/- 1.51 mg mg(-1)干重)样品与我们提出的方法(12.95 +/- 1.55 mg mg(-1)干重)之间的羟脯氨酸含量没有显着差异。使用SEM显微照片评估支架的形态和细胞附着,并用无去污剂的脱细胞CEbS接种14、21和28天的细胞覆盖了支架区域,包括多孔腔。显微镜观察表明,细胞密度每天都在增加,没有关于支架的细胞毒性证据,这是细胞理想的环境。组织化学和免疫组织化学评估得到糖胺聚糖和羟脯氨酸分析的支持。提出的无去污剂脱细胞技术可能是一种有前景的软骨组织再生方法。

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