Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector

Background: Using recombinant adeno-associated virus 2 (rAAV-2), we attempted to establish a HEK293T cell line that is able to site-specifically integrate and stably express glial cell line-derived neurotrophic factor (GDNF). Results:Recombinant vector with enhanced green fluorescent protein (EGFP) and GDNF (pTR-P5-EGFP-IRES-GDNF), as well as that carrying Rep genes and SV40 promoters (pSVAV2) were constructed and packed. HEK293T cells were co-infected with rAAV-2/EGFP-GDNF and rAAV-2/SVAV2 virus separately at 1 x 10(4),1 x 10(5),and 1x10(6) of multiplicity of infection (MOI). The efficiency of transduction was detected using flow cytometry. Additionally, the infected HEK293T cells were separately validated by touchdown polymerase chain reaction (PCR) and Western-blot. After 72 h of transduction, the rate of EGFP positive cell was 22%, 45% and 49% at the MOIs of 1 x 10(4),1 x 10(5) and 1 x 10(6), respectively. On the 3rd, 6th and 9th day of cell passage, there was no significant difference in the cell viability and proliferation rate between transduction and control groups. Importantly, touchdown PCR showed that there was a specific PCR amplified product band in the lane of infected cells. Furthermore, GDNF expression was detected in the infected cells after 15 and 180 d of cultivation. Conclusions: A HEK293T cell line able to site-specifically integrate and stably express GDNF was established.

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Main Authors: Zhang,Jinju, Zhang,Yun, Liu,Xiaomei, Xiang,Jingjing, Zhang,Chun
Format: Digital revista
Language:English
Published: Pontificia Universidad Católica de Valparaíso 2016
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400011
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spelling oai:scielo:S0717-345820160004000112016-09-13Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vectorZhang,JinjuZhang,YunLiu,XiaomeiXiang,JingjingZhang,Chun Glial cell line-derived neurotrophic factor Multiplicity of infection Recombinant adeno-associated virus 2 Site-specific integration Transduction Background: Using recombinant adeno-associated virus 2 (rAAV-2), we attempted to establish a HEK293T cell line that is able to site-specifically integrate and stably express glial cell line-derived neurotrophic factor (GDNF). Results:Recombinant vector with enhanced green fluorescent protein (EGFP) and GDNF (pTR-P5-EGFP-IRES-GDNF), as well as that carrying Rep genes and SV40 promoters (pSVAV2) were constructed and packed. HEK293T cells were co-infected with rAAV-2/EGFP-GDNF and rAAV-2/SVAV2 virus separately at 1 x 10(4),1 x 10(5),and 1x10(6) of multiplicity of infection (MOI). The efficiency of transduction was detected using flow cytometry. Additionally, the infected HEK293T cells were separately validated by touchdown polymerase chain reaction (PCR) and Western-blot. After 72 h of transduction, the rate of EGFP positive cell was 22%, 45% and 49% at the MOIs of 1 x 10(4),1 x 10(5) and 1 x 10(6), respectively. On the 3rd, 6th and 9th day of cell passage, there was no significant difference in the cell viability and proliferation rate between transduction and control groups. Importantly, touchdown PCR showed that there was a specific PCR amplified product band in the lane of infected cells. Furthermore, GDNF expression was detected in the infected cells after 15 and 180 d of cultivation. Conclusions: A HEK293T cell line able to site-specifically integrate and stably express GDNF was established.info:eu-repo/semantics/openAccessPontificia Universidad Católica de ValparaísoElectronic Journal of Biotechnology v.19 n.4 20162016-07-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400011en10.1016/j.ejbt.2016.05.001
institution SCIELO
collection OJS
country Chile
countrycode CL
component Revista
access En linea
databasecode rev-scielo-cl
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region America del Sur
libraryname SciELO
language English
format Digital
author Zhang,Jinju
Zhang,Yun
Liu,Xiaomei
Xiang,Jingjing
Zhang,Chun
spellingShingle Zhang,Jinju
Zhang,Yun
Liu,Xiaomei
Xiang,Jingjing
Zhang,Chun
Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector
author_facet Zhang,Jinju
Zhang,Yun
Liu,Xiaomei
Xiang,Jingjing
Zhang,Chun
author_sort Zhang,Jinju
title Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector
title_short Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector
title_full Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector
title_fullStr Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector
title_full_unstemmed Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector
title_sort establishment of a hek293t cell line able to site-specifically integrate and stably express gdnf by raav-2 vector
description Background: Using recombinant adeno-associated virus 2 (rAAV-2), we attempted to establish a HEK293T cell line that is able to site-specifically integrate and stably express glial cell line-derived neurotrophic factor (GDNF). Results:Recombinant vector with enhanced green fluorescent protein (EGFP) and GDNF (pTR-P5-EGFP-IRES-GDNF), as well as that carrying Rep genes and SV40 promoters (pSVAV2) were constructed and packed. HEK293T cells were co-infected with rAAV-2/EGFP-GDNF and rAAV-2/SVAV2 virus separately at 1 x 10(4),1 x 10(5),and 1x10(6) of multiplicity of infection (MOI). The efficiency of transduction was detected using flow cytometry. Additionally, the infected HEK293T cells were separately validated by touchdown polymerase chain reaction (PCR) and Western-blot. After 72 h of transduction, the rate of EGFP positive cell was 22%, 45% and 49% at the MOIs of 1 x 10(4),1 x 10(5) and 1 x 10(6), respectively. On the 3rd, 6th and 9th day of cell passage, there was no significant difference in the cell viability and proliferation rate between transduction and control groups. Importantly, touchdown PCR showed that there was a specific PCR amplified product band in the lane of infected cells. Furthermore, GDNF expression was detected in the infected cells after 15 and 180 d of cultivation. Conclusions: A HEK293T cell line able to site-specifically integrate and stably express GDNF was established.
publisher Pontificia Universidad Católica de Valparaíso
publishDate 2016
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400011
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