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功能性β细胞的成熟表现为葡萄糖阈值升高和尿皮质素 3 的表达。

Functional beta-cell maturation is marked by an increased glucose threshold and by expression of urocortin 3.

机构信息

Department of Stem Cell and Regenerative Biology, Harvard Stem Cell Institute, Harvard University, Cambridge, Massachusetts, USA.

出版信息

Nat Biotechnol. 2012 Feb 26;30(3):261-4. doi: 10.1038/nbt.2141.

DOI:10.1038/nbt.2141
PMID:22371083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4617627/
Abstract

Insulin-expressing cells that have been differentiated from human pluripotent stem cells in vitro lack the glucose responsiveness characteristic of mature beta cells. Beta-cell maturation in mice was studied to find genetic markers that enable screens for factors that induce bona fide beta cells in vitro. We find that functional beta-cell maturation is marked by an increase in the glucose threshold for insulin secretion and by expression of the gene urocortin 3.

摘要

在体外从人类多能干细胞分化而来的表达胰岛素的细胞缺乏成熟β细胞的葡萄糖反应性特征。为了寻找能够在体外诱导真正的β细胞的因子的筛选遗传标记,研究了小鼠β细胞的成熟。我们发现,功能性β细胞成熟的标志是胰岛素分泌的葡萄糖阈值增加和 Urocortin 3 基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a4/4617627/698bcfe02113/nihms616141f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a4/4617627/118ee39d5193/nihms616141f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a4/4617627/698bcfe02113/nihms616141f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a4/4617627/118ee39d5193/nihms616141f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a4/4617627/698bcfe02113/nihms616141f2.jpg

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Production of functional glucagon-secreting α-cells from human embryonic stem cells.人胚胎干细胞来源的功能性胰高血糖素分泌α细胞的生成。
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MafA and MafB regulate genes critical to beta-cells in a unique temporal manner.MafA 和 MafB 以独特的时间方式调节β细胞中至关重要的基因。
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Epigenetic memory as crucial contributing factor in directing the differentiation of human iPSC into pancreatic β-cells in vitro.表观遗传记忆作为体外引导人诱导多能干细胞分化为胰腺β细胞的关键促成因素。
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