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从神经基因 3/EGFP 转基因小鼠发育中的胰腺中纯化和鉴定一群表达 EGFP 的细胞。

Purification and Characterization of a Population of EGFP-Expressing Cells from the Developing Pancreas of a Neurogenin3/EGFP Transgenic Mouse.

机构信息

School of Medical Sciences; University of Aberdeen; Institute of Medical Sciences; Foresterhill, Aberdeen UK.

出版信息

Organogenesis. 2005 Jan;2(1):22-7. doi: 10.4161/org.2.1.1727.

Abstract

Neurogenin 3 (ngn3) is a basic helix loop helix transcription factor that is transiently expressed in the developing mouse pancreas with peak expression around E15. In mice lacking the ngn3 gene the endocrine cells of the pancreas fail to develop suggesting that the ngn3-positive cell may represent a progenitor cell for the endocrine pancreas. In order to purify and characterize this cell in detail we have generated a transgenic mouse, in which the ngn3 promoter drives expression of enhanced green fluorescent protein (EGFP). In the E15.5 embryo EGFP was expressed in the dorsal and ventral pancreas, the duodenum, and lower intestine as well as in the brain. This pattern of expression was in keeping with the known expression profile of the endogenous ngn3 gene. Within the pancreas EGFP was localized in close proximity to cells that stained positive for ngn3, insulin, and glucagon, but was absent from regions of the pancreas that stained positive for amylase. EGFP was also present in the pancreas at E18.5, although there was no detectable expression of ngn3. At this stage EGFP did not colocalize with any of the hormones or exocrine markers. EGFP(+) cells were FACS purified (96%) from the E15 pancreas yielding approximately 10,000 cells or 1.6% of the total pancreatic cells from one litter. RT/PCR analysis confirmed that the purified cells expressed EGFP, ngn3, insulin, glucagon, somatostatin and pancreatic polypeptide. The ability to purify ngn3(+) cells provides an invaluable source of material for charactering in detail their properties.

摘要

神经基因 3(ngn3)是一种基本螺旋环螺旋转录因子,在发育中的小鼠胰腺中短暂表达,在 E15 左右表达达到峰值。在缺乏 ngn3 基因的小鼠中,胰腺内分泌细胞未能发育,这表明 ngn3 阳性细胞可能代表内分泌胰腺的祖细胞。为了详细地纯化和表征这种细胞,我们生成了一种转基因小鼠,其中 ngn3 启动子驱动增强型绿色荧光蛋白(EGFP)的表达。在 E15.5 胚胎中,EGFP 在背侧和腹侧胰腺、十二指肠和下肠以及大脑中表达。这种表达模式与内源性 ngn3 基因的已知表达谱一致。在胰腺中,EGFP 与 ngn3、胰岛素和胰高血糖素染色阳性的细胞紧密相邻,但不存在于胰腺中淀粉酶染色阳性的区域。在 E18.5,EGFP 也存在于胰腺中,尽管没有检测到 ngn3 的表达。在这个阶段,EGFP 与任何激素或外分泌标志物都没有共定位。EGFP(+)细胞从 E15 胰腺中通过 FACS 纯化(96%),大约获得 10,000 个细胞或一个窝仔中总胰腺细胞的 1.6%。RT/PCR 分析证实纯化的细胞表达 EGFP、ngn3、胰岛素、胰高血糖素、生长抑素和胰多肽。纯化 ngn3(+)细胞的能力为详细表征其特性提供了宝贵的材料来源。

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