小鼠神经原素3单克隆抗体的制备:研究胰腺内分泌祖细胞的一种新的免疫细胞化学工具。

Stefan Zahn, Jakob Hecksher-Sørensen, Inger Lund Pedersen, Palle Serup, Ole Madsen
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引用次数: 23

摘要

未分化前体细胞诱导胰腺内分泌分化是一个受多种转录因子表达调控的多步骤过程。在E9.5时,同源结构域蛋白Pdx-1的表达定义了早期胰腺上皮。随后,基本螺旋-环-螺旋因子Neurogenin 3 (Ngn3)的表达标志着胰腺前体细胞内分泌谱系的开始。为了在体外控制胚胎干细胞分泌胰岛素的β细胞的发育,充分了解这些过程是必不可少的。由于ngn3的表达是关键步骤,因此本研究的目的是开发用于免疫组化(IHC)检测ngn3的单克隆抗体。所有用重组GST-mNGN3融合蛋白免疫的小鼠(rbf -株)均产生高抗体效价。在胚胎(E13)小鼠胰腺石蜡切片上进一步通过免疫组化筛选血清,随后从一只小鼠获得的两个杂杂瘤产生了具有突出和特异性Ngn3染色特性的抗体。这些新抗体为共标记研究提供了新的有用的工具,利用大量现有的兔多克隆抗体可针对重要的转录因子,进一步表征胰腺内分泌祖细胞的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generation of monoclonal antibodies against mouse neurogenin 3: a new immunocytochemical tool to study the pancreatic endocrine progenitor cell.

The induction of pancreatic endocrine differentiation from undifferentiated precursor cells is a multi-step process regulated by the expression of several transcription factors. At E9.5 expression of homeodomain protein Pdx-1 defines the early pancreatic epithelium. Later, expression of the basic helix-loop-helix factor, Neurogenin 3 (Ngn3) marks the initiation of the endocrine lineage from the pancreatic precursor cells. A full understanding of these processes is essential in order to control development of insulin secreting beta-cells from embryonic stem cells in vitro. Since the expression of ngn3 is a key step, the aim of this work was to develop monoclonal antibodies for immunohistochemical (IHC) detection of Ngn3. All mice (RBF-strain) immunized with recombinant GST-mNGN3 fusion protein responded with a high antibody titer. The sera were further screened by IHC on paraffin sections of fetal (E13) mouse pancreas, and two hybridomas subsequently derived from one selected mouse produced antibodies with prominent and specific Ngn3 staining properties. These new antibodies provide novel useful tools for co-labeling studies using the large panel of existing rabbit polyclonal antibodies available against important transcription factors to further characterize the development of pancreatic endocrine progenitor cells.

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