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通过对胰腺十二指肠同源异型盒因子 1 启动子的表观遗传调控,从 CD44+/CD105+ 人羊水诱导产生胰腺 β 样细胞。

Induction of pancreatic β-cell-like cells from CD44+/CD105+ human amniotic fluids via epigenetic regulation of the pancreatic and duodenal homeobox factor 1 promoter.

机构信息

Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.

出版信息

DNA Cell Biol. 2011 Sep;30(9):739-48. doi: 10.1089/dna.2010.1144. Epub 2011 May 25.

Abstract

Pancreatic and duodenal homeobox factor 1 (PDX-1) maintains β-cell function and differentiation via direct regulation of multiple islet cell genes. However, the molecular mechanisms involved in this process remain unknown. Here, we show that PDX-1 plays an important role in the induction of CD44+/CD105+ human amniotic fluid cells (HuAFCs) into functional pancreatic β-cell-like cells in vitro. CD44+/CD105+ HuAFCs were transfected with either siRNA targeting PDX-1 (siRNA-PDX-1) or mock plasmid (siRNA-MOCK). Following induction, siRNA-MOCK-transfected cells differentiated into β-cell-like cells that expressed multiple islet cell markers and produced insulin and C-peptide in a glucose-regulated manner. However, siRNA-PDX-1-transfected cells did not fully differentiate into β-cell-like cells. Further, we observed epigenetic changes at the PDX-1 gene locus in induced CD44(+)/CD105(+) HuAFCs. Therefore, CD44+/CD105+ HuAFCs could be a source of human pancreatic β-cell-like cells with potential uses in cell replacement therapy for diabetes.

摘要

胰腺十二指肠同源盒因子 1(PDX-1)通过直接调控多种胰岛细胞基因来维持β细胞的功能和分化。然而,这一过程中涉及的分子机制尚不清楚。在这里,我们证明 PDX-1 在体外诱导 CD44+/CD105+人羊水细胞(HuAFCs)分化为功能性胰腺β细胞样细胞中发挥重要作用。CD44+/CD105+ HuAFCs 转染靶向 PDX-1 的 siRNA(siRNA-PDX-1)或 mock 质粒(siRNA-MOCK)。诱导后,siRNA-MOCK 转染的细胞分化为表达多种胰岛细胞标志物并以葡萄糖调节方式分泌胰岛素和 C 肽的β细胞样细胞。然而,siRNA-PDX-1 转染的细胞不能完全分化为β细胞样细胞。此外,我们观察到诱导的 CD44(+)/CD105(+) HuAFCs 中 PDX-1 基因座的表观遗传变化。因此,CD44+/CD105+ HuAFCs 可能是人类胰腺β细胞样细胞的来源,在糖尿病的细胞替代治疗中有潜在的应用价值。

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