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Differentiation of Human-Induced Pluripotent Stem Cells Into Insulin-Producing Clusters by MicroRNA-7

机译:MicroRNA-7将人诱导的多能干细胞分化为胰岛素产生簇。

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Objectives: Diabetes results from inadequate insulin production from pancreatic β-cells. Islet cell replacement is an effective approach for diabetes treatment; however, it is not sufficient for all diabetic patients. Thus, finding a new source with effective maturation of β-cells is the major goal of many studies. MicroRNAs are a class of small noncoding ribonucleic acid that regulate gene expression through posttranscriptional mechanisms. MicroRNA-7 has high expression level during pancreatic islet development in humans, thereby playing a critical role in pancreatic β-cell function. We study aimed to develop a protocol to differentiate human-induced pluripotent stem cells efficiently into isletlike cell clusters in vitro by using microRNA-7. Materials and Methods: Human-induced pluripotent stem cell colonies were transfected with hsa-microRNA-7 by using siPORT NeoFX transfection agent. Total ribonucleic acid was extracted 24 and 48 hours after transfection. The expression of transcription factors which were important during pancreases development was also performed. On the third day, the potency of the clusters was assessed in response to high glucose levels. Diphenylthiocarbazone was used to identify the existence of the β-cells. The presence of insulin and Neurogenin-3 proteins was investigated by immunocytochemistry. Results: Morphologic changes were observed on the first day after chemical transfection, and cell clusters were formed on the third day. The expression of pancreatic specific transcription factors was increased on the first day and significantly increased on the second day. The isletlike cell clusters were positive for insulin and Neurogenin-3 proteins in immuno-cytochemistry. The clusters were stained with Diphenylthiocarbazone and secreted insulin in a glucose challenge test. Conclusions: MicroRNA-7 transcription factor net-work is important in pancreatic endocrine differe-ntiation. Chemical transfection with microRNA-7 can differentiate human induced pluripotent stem cells into functional isletlike cell clusters in a short time.
机译:目的:糖尿病是由胰腺β细胞产生的胰岛素不足引起的。胰岛细胞替代是治疗糖尿病的有效方法。但是,对于所有糖尿病患者而言,这还不够。因此,寻找有效成熟β细胞的新来源是许多研究的主要目标。 MicroRNA是一类小的非编码核糖核酸,可通过转录后机制调节基因表达。 MicroRNA-7在人类胰岛发育过程中具有高表达水平,因此在胰腺β细胞功能中起着至关重要的作用。我们研究旨在开发一种协议,通过使用microRNA-7在体外将人诱导的多能干细胞有效地分化为胰岛样细胞簇。材料和方法:使用siPORT NeoFX转染剂,用hsa-microRNA-7转染人诱导的多能干细胞集落。转染后24和48小时提取总核糖核酸。还进行了在胰腺发育过程中重要的转录因子的表达。在第三天,评估簇的效力以响应高葡萄糖水平。二苯硫卡巴zone被用来鉴定β细胞的存在。通过免疫细胞化学研究了胰岛素和Neurogenin-3蛋白的存在。结果:化学转染后第一天观察到形态变化,第三天形成细胞团。胰腺特异性转录因子的表达在第一天增加,第二天显着增加。胰岛样细胞簇在免疫细胞化学中对胰岛素和Neurogenin-3蛋白呈阳性。用二苯基硫代卡巴s对簇染色,并在葡萄糖激发试验中分泌胰岛素。结论:MicroRNA-7转录因子网络在胰腺内分泌分化中起重要作用。用microRNA-7进行化学转染可以在短时间内将人诱导的多能干细胞分化为功能性胰岛样细胞簇。

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