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脊索对内胚层音猬因子的抑制作用可促进胰腺发育。

Notochord repression of endodermal Sonic hedgehog permits pancreas development.

作者信息

Hebrok M, Kim S K, Melton D A

机构信息

Department of Molecular and Cellular Biology and Howard Hughes Medical Institute, Harvard University, Cambridge, Massachusetts 02138 USA.

出版信息

Genes Dev. 1998 Jun 1;12(11):1705-13. doi: 10.1101/gad.12.11.1705.

Abstract

Notochord signals to the endoderm are required for development of the chick dorsal pancreas. Sonic hedgehog (SHH) is normally absent from pancreatic endoderm, and we provide evidence that notochord, in contrast to its effects on adjacent neuroectoderm where SHH expression is induced, represses SHH expression in adjacent nascent pancreatic endoderm. We identify activin-betaB and FGF2 as notochord factors that can repress endodermal SHH and thereby permit expression of pancreas genes including Pdx1 and insulin. Endoderm treatment with antibodies that block hedgehog activity also results in pancreatic gene expression. Prevention of SHH expression in prepancreatic dorsal endoderm by intercellular signals, like activin and FGF, may be critical for permitting early steps of chick pancreatic development.

摘要

脊索向内胚层发出的信号是鸡背侧胰腺发育所必需的。胰腺内胚层通常不存在音猬因子(SHH),并且我们提供的证据表明,与它对诱导SHH表达的相邻神经外胚层的作用相反,脊索抑制相邻新生胰腺内胚层中的SHH表达。我们确定激活素-βB和FGF2为脊索因子,它们可抑制内胚层SHH,从而使包括Pdx1和胰岛素在内的胰腺基因得以表达。用阻断刺猬蛋白活性的抗体处理内胚层也会导致胰腺基因表达。通过细胞间信号(如激活素和FGF)防止胰腺前背侧内胚层中的SHH表达,对于鸡胰腺发育的早期步骤可能至关重要。

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