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肝细胞核因子6(Hnf6)和转录因子2(Tcf2,即青少年发病的成年型糖尿病5型,MODY5)在胚胎胰腺前体细胞区域运作的基因网络中相互关联。

Hnf6 and Tcf2 (MODY5) are linked in a gene network operating in a precursor cell domain of the embryonic pancreas.

作者信息

Maestro Miguel A, Boj Sylvia F, Luco Reini F, Pierreux Christophe E, Cabedo Judit, Servitja Joan M, German Michael S, Rousseau Guy G, Lemaigre Frederic P, Ferrer Jorge

机构信息

Endocrinology, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

出版信息

Hum Mol Genet. 2003 Dec 15;12(24):3307-14. doi: 10.1093/hmg/ddg355. Epub 2003 Oct 21.

Abstract

During pancreatic organogenesis endocrine cells arise from non self-renewing progenitors that express Ngn3. The precursors that give rise to Ngn3+ cells are presumably located within duct-like structures. However, the nature of such precursors is poorly understood. We show that, at E13-E18, the embryonic stage during which the major burst of beta-cell neogenesis takes place, pancreatic duct cells express Hnf1beta, the product of the maturity-onset diabetes of the young type 5 (MODY5) gene. Ngn3+ cells at this stage invariably cluster with mitotically competent Hnf1beta+ cells, and are often intercalated with these cells in the epithelium that lines the lumen of primitive ducts. We present several observations that collectively indicate that Hnf1beta+ cells are the immediate precursors of Ngn3+ cells. We furthermore show that Hnf1beta expression is markedly reduced in early pancreatic epithelial cells of Hnf6-deficient mice, in which formation of Ngn3+ cells is defective. These findings define a precursor cellular stage of the embryonic pancreas and place Hnf1beta in a genetic hierarchy that regulates the generation of pancreatic endocrine cells.

摘要

在胰腺器官发生过程中,内分泌细胞起源于表达Ngn3的非自我更新祖细胞。产生Ngn3+细胞的前体细胞大概位于导管样结构内。然而,此类前体细胞的本质却知之甚少。我们发现,在E13 - E18(即β细胞新生主要爆发的胚胎阶段),胰腺导管细胞表达Hnf1β,它是年轻型5型成年发病型糖尿病(MODY5)基因的产物。此阶段的Ngn3+细胞总是与有丝分裂活性的Hnf1β+细胞聚集在一起,并且常常在原始导管管腔内衬的上皮中与这些细胞相互嵌插。我们提供了多项观察结果,共同表明Hnf1β+细胞是Ngn3+细胞的直接前体细胞。我们还进一步表明,在Ngn3+细胞形成存在缺陷的Hnf6缺陷小鼠的早期胰腺上皮细胞中,Hnf1β的表达明显降低。这些发现定义了胚胎胰腺的一个前体细胞阶段,并将Hnf1β置于调控胰腺内分泌细胞生成的遗传层级中。

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