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融合表达载体EGFP-PDX-1的构建及其通过电穿孔法转染大鼠胎肝干细胞

[Construction of fusion expression vector EGFP-PDX-1 and its transfection into rat fetal hepatic stem cells by electroporation].

作者信息

Sun Bing, Sun Xiao-yan, An Jing

机构信息

Department of Histology and Embryology, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2006 Jun;26(6):750-3.

Abstract

OBJECTIVE

To construct the fusion expression vector of pancreatic-duodenal homeobox gene 1 (PDX-1) fused to green fluorescent protein (GFP) capable of stable expression in fetal rat hepatic stem cells after transfection by electroporation.

METHODS

PDX-1 cDNA was amplified from SK900/BLSCRIPT plasmid and cloned into the multiple cloning site of pEGFP-C1 to obtain the recombined plasmid pEGFP-C1-PDX-1. Rat fetal hepatic stem cells were isolated, cultured, identified and transfected with the recombinant vector by electroporation, followed by observation of these cells with fluorescent microscope. The result of transfection was analyzed by RT-PCR and cell growth curve.

RESULTS

Identification by enzyme digestion confirmed successful construction of the recombinant vector. Fetal hepatic stem cells can stably express GFP and PDX-1 for a period of time, and their growth and proliferation was not obviously affected after transfection.

CONCLUSION

The fusion expression vector of EGFP-PDX-1 is successfully constructed and stably expressed in rat fetal hepatic stem cells, which may facilitate the study of the role of PDX-1 in stem cell differentiation into insulin-producing cells.

摘要

目的

构建胰腺十二指肠同源盒基因1(PDX-1)与绿色荧光蛋白(GFP)融合的表达载体,经电穿孔转染后能在胎鼠肝干细胞中稳定表达。

方法

从SK900/BLSCRIPT质粒中扩增PDX-1 cDNA,并克隆到pEGFP-C1的多克隆位点,获得重组质粒pEGFP-C1-PDX-1。分离、培养、鉴定胎鼠肝干细胞,用电穿孔法将重组载体转染至细胞,随后用荧光显微镜观察这些细胞。通过RT-PCR和细胞生长曲线分析转染结果。

结果

酶切鉴定证实重组载体构建成功。胎肝干细胞可在一段时间内稳定表达GFP和PDX-1,转染后其生长和增殖未受到明显影响。

结论

成功构建了EGFP-PDX-1融合表达载体并在胎鼠肝干细胞中稳定表达,这可能有助于研究PDX-1在干细胞分化为胰岛素分泌细胞中的作用。

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