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首页> 外文期刊>Journal of Tissue Engineering >Analysis of type II diabetes mellitus adipose-derived stem cells for tissue engineering applications
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Analysis of type II diabetes mellitus adipose-derived stem cells for tissue engineering applications

机译:组织工程应用中II型糖尿病脂肪干细胞的分析

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To address the functionality of diabetic adipose-derived stem cells in tissue engineering applications, adipose-derived stem cells isolated from patients with and without type II diabetes mellitus were cultured in bioreactor culture systems. The adipose-derived stem cells were differentiated into adipocytes and maintained as functional adipocytes. The bioreactor system utilizes a hollow fiber–based technology for three-dimensional perfusion of tissues in vitro, creating a model in which long-term culture of adipocytes is feasible, and providing a potential tool useful for drug discovery. Daily metabolic activity of the adipose-derived stem cells was analyzed within the medium recirculating throughout the bioreactor system. At experiment termination, tissues were extracted from bioreactors for immunohistological analyses in addition to gene and protein expression. Type II diabetic adipose-derived stem cells did not exhibit significantly different glucose consumption compared to adipose-derived stem cells from patients without type II diabetes (p?>?0.05, N?=?3). Expression of mature adipocyte genes was not significantly different between diabeticon-diabetic groups (p?>?0.05, N?=?3). Protein expression of adipose tissue grown within all bioreactors was verified by Western blotting.The results from this small-scale study reveal adipose-derived stem cells from patients with type II diabetes when removed from diabetic environments behave metabolically similar to the same cells of non-diabetic patients when cultured in a three-dimensional perfusion bioreactor, suggesting that glucose transport across the adipocyte cell membrane, the hindrance of which being characteristic of type II diabetes, is dependent on environment. The presented observation describes a tissue-engineered tool for long-term cell culture and, following future adjustments to the culture environment and increased sample sizes, potentially for anti-diabetic drug testing.
机译:为了解决糖尿病性脂肪干细胞在组织工程应用中的功能,在生物反应器培养系统中培养分离自患有和不患有II型糖尿病患者的脂肪干细胞。脂肪干细胞分化为脂肪细胞并维持为功能性脂肪细胞。生物反应器系统利用基于中空纤维的技术在体外对组织进行三维灌注,从而创建了一种模型,其中脂肪细胞的长期培养是可行的,并为药物发现提供了潜在的工具。在整个生物反应器系统中循环的培养基中分析了脂肪干细胞的每日代谢活性。在实验终止时,除了基因和蛋白质表达外,还从生物反应器中提取组织用于免疫组织学分析。与非II型糖尿病患者的脂肪干细胞相比,II型糖尿病脂肪干细胞的葡萄糖消耗没有显着差异(p≥0.05,N≥3)。在糖尿病/非糖尿病组之间,成熟脂肪细胞基因的表达没有显着差异(p≥0.05,N≥3)。通过蛋白质印迹法验证了所有生物反应器中生长的脂肪组织的蛋白质表达。这项小规模研究的结果表明,从糖尿病环境中取出的II型糖尿病患者的脂肪干细胞在代谢上的行为类似于非糖尿病患者的相同细胞。糖尿病患者在三维灌注生物反应器中培养时,提示葡萄糖穿过脂肪细胞膜的转运取决于环境,而后者是II型糖尿病的特征。提出的观察结果描述了一种组织工程化的工具,用于长期细胞培养,并且在将来对培养环境进行调整并增加了样本量之后,有可能用于抗糖尿病药物测试。

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