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Generation and Characterization of Ptf1a Antiserum and Localization of Ptf1a in Relation to Nkx6.1 and Pdx1 During the Earliest Stages of Mouse Pancreas Development

机译:Ptf1a抗血清的生成和表征以及与小鼠胰腺发育早期有关的Nkx6.1和Pdx1的Ptf1a定位

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摘要

Ptf1a and Pdx1 are critical transcription factors of early pancreatic development, as shown by loss of function studies where lack of each gene alone causes almost complete pancreas agenesis. Ptf1a is particularly interesting because it is linked to a recently reported signature gene expression profile associated with the multipotent condition. Few useful antibody reagents have been available for consistent and reliable immunohistochemical visualization of Ptf1a protein expression in the early developing pancreas in which the level of production of this critical regulator seems to be very low. We describe a novel rabbit antibody raised against the c-terminal portion of the mouse Ptf1a protein and report immunodetection, for the first time, as early as embryonic day (e) 8.5–e8.75 in the dorsal and ventral buds of the mouse pancreas as well as in the neural tube at e10.0. Detailed confocal analysis identifies an abundant triple-positive (Ptf1a+/Nkx6.1+/Pdx1+) putative early multipotent pancreatic progenitor cell that marks the e9.5 dorsal pancreas and e10.5 ventral pancreas. Furthermore, expression patterns of Nkx6.1 vs Ptf1a subsequently segregate during branching morphogenesis (trunk vs tip), ending up marking two distinct cell populations of progenitors at e12.5. From e15.5 (mouse) and in adult pancreas (mouse, rat, and human), the Ptf1a antibody marks only acinar cell nuclei, as expected for its subsequent role in committing/maintaining cells in this differentiated state. In summary, this antibody is a novel tool to further characterize important early steps of pancreas differentiation. This manuscript contains online supplemental material at http://www.jhc.org. Please visit this article online to view these materials. (J Histochem Cytochem 56:587–595, 2008)
机译:Ptf1a和Pdx1是早期胰腺发育的关键转录因子,功能丧失研究表明,其中每个基因的缺乏单独导致几乎完全的胰腺发育不全。 Ptf1a特别有趣,因为它与最近报道的与多能性疾病相关的签名基因表达谱相关。很少有有用的抗体试剂可用于早期发育的胰腺中Ptf1a蛋白表达的一致和可靠的免疫组化可视化,在该胰腺中该关键调节因子的产生水平似乎很低。我们描述了一种新型的针对兔Ptf1a蛋白c端部分的兔抗体,并首次报告了免疫检测,最早是在小鼠胰腺的背侧和腹侧胚芽(e)8.5–e8.75以及在e10.0的神经管中。详细的共聚焦分析确定了丰富的三阳性(Ptf1a + / Nkx6.1 + / Pdx1 +)假定的早期多能胰腺祖细胞,该细胞标记了e9.5背胰腺和e10.5腹胰腺。此外,Nkx6.1与Ptf1a的表达模式随后在分支形态发生过程中分离(树干与末端),最终在e12.5处标记了两个不同的祖细胞群。从e15.5(小鼠)到成年胰腺(小鼠,大鼠和人),Ptf1a抗体仅标记腺泡细胞核,正如其在此分化状态下定型/维持细胞的后续作用所期望的那样。总之,该抗体是进一步表征胰腺分化重要早期步骤的新型工具。该手稿包含在线补充材料,网址为http://www.jhc.org。请在线访问本文以查看这些材料。 (J Histochem Cytochem 56:587–595,2008)

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