Coexpression of recombinant adenovirus carrying GDNF and EDNRB genes in neural stem cells in vitro

Gene therapy and nerve stem cells isolated from the developing human enteric nervous system (ENS) are significant. They may open the route for the cell therapy of Hirschsprung's disease (HD). We have constructed the recombinant adenovirus‐carrying glial cell line‐derived neurotrophic factor (GD...

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Published inCell biology international Vol. 37; no. 5; pp. 458 - 463
Main Authors Sun, Nian-Feng, Zhong, Wen-Yu, Lu, Sheng-Ai, Tian, Yu-Ling, Chen, Jing-Bo, Hu, San-Yuan, Tian, Ai-Ling
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.05.2013
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Summary:Gene therapy and nerve stem cells isolated from the developing human enteric nervous system (ENS) are significant. They may open the route for the cell therapy of Hirschsprung's disease (HD). We have constructed the recombinant adenovirus‐carrying glial cell line‐derived neurotrophic factor (GDNF) and endothelin receptor B (EDNRB) gene, and investigated the exosomatic coexpression in neural stem cells. The recombinant adenovirus Ad‐GE coexpressing GDNF and EDNRB gene was constructed by the AdEasy system and confirmed by the reverse transcription polymerase chain reaction (RT‐PCR) method. Expression of exogenous genes in neural stem cells after transfection was confirmed by the flow cytometry and real‐time fluorescence quantitative PCR. Fragments of pAd Track‐CMV‐GE were consistent with GDNF and EDNRB. The green fluorescence of the positive cells was followed by fluorescence microscopy at 24 h after NSCs had been transfected, reaching a peak at 72 h after transfection. Flow cytometry showed that the efficiency of transfection was 15.0, 23.6, and 25.4% at 24, 48 and 72 h respectively. Real‐time fluorescence quantitative PCR showed the expression levels of mRNA of GDNF and EDNRB in 48 and 72 h groups were obviously higher than that in 24 and 96 h groups. Recombinant adenovirus carrying GDNF and EDNRB genes are coexpressed in neural stem cells, which may offer the possibility of a novel approach to local combination gene therapy for Hirschsprung's disease.
Bibliography:Independent Innovation Foundation of Shandong University - No. 2011JC016
ArticleID:CBIN10060
ark:/67375/WNG-N2BZPG01-M
China Postdoctoral Science - No. 20100481271
Natural Science Foundation of Shandong Province - No. ZR2012HM002
istex:F228CCD305257D0885160FEB6BF04C9E42B9E09C
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1065-6995
1095-8355
DOI:10.1002/cbin.10060