Construction of fusion expression vector EGFP-PDX-1 and its transfection into rat fetal hepatic stem cells by electroporation.
- Author:
Bing SUN
1
;
Xiao-yan SUN
;
Jing AN
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Electroporation; Female; Fetal Stem Cells; cytology; metabolism; Gene Expression; Genetic Vectors; genetics; Green Fluorescent Proteins; biosynthesis; genetics; Hepatocytes; cytology; metabolism; Homeodomain Proteins; biosynthesis; genetics; Pregnancy; Rats; Rats, Sprague-Dawley; Recombinant Fusion Proteins; biosynthesis; genetics; Reverse Transcriptase Polymerase Chain Reaction; Trans-Activators; biosynthesis; genetics; Transfection; methods
- From: Journal of Southern Medical University 2006;26(6):750-753
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo 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.
METHODSPDX-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.
RESULTSIdentification 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.
CONCLUSIONThe 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.