Journal of Southern Medical University ›› 2006, Vol. 26 ›› Issue (06): 750-753.

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

SUN Bing1, SUN Xiao-yan2, AN Jing1 1Department of Histology and Embryology, Southern Medical University, Guangzhou 510515, China; 2Institute of Basic Medical Sciences, General Hospital of PLA, Beijing 100853, China   

  1. 南方医科大学组织胚胎学教研室; 解放军总医院基础医学研究所; 南方医科大学组织胚胎学教研室 广东广州510515; 北京100853; 广东广州510515;
  • Online:2006-06-20 Published:2006-06-20

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 tranfection 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. 

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