Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression

The human embryonic stem cell (hESC) line NERCe003-A-1 was generated by introducing lentiviral-vector–mediated tetracycline-inducible β-catenin expression into a normal hESC line, NERCe003-A. The resulting cell line can overexpress the β-catenin protein, encoded by the CTNNB1 gene, after exposure to...

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Main Authors: Yang Wang, Juan Yu, Lvjun Liu, Wen Li, Xingxiang Duan, Yingying Peng, Sicong Zeng, Qi Ouyang, Guangxiu Lu, Ge Lin, Yi Sun
Format: Article
Language:English
Published: Elsevier 2018-04-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506118300266
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author Yang Wang
Juan Yu
Lvjun Liu
Wen Li
Xingxiang Duan
Yingying Peng
Sicong Zeng
Qi Ouyang
Guangxiu Lu
Ge Lin
Yi Sun
author_facet Yang Wang
Juan Yu
Lvjun Liu
Wen Li
Xingxiang Duan
Yingying Peng
Sicong Zeng
Qi Ouyang
Guangxiu Lu
Ge Lin
Yi Sun
author_sort Yang Wang
collection DOAJ
description The human embryonic stem cell (hESC) line NERCe003-A-1 was generated by introducing lentiviral-vector–mediated tetracycline-inducible β-catenin expression into a normal hESC line, NERCe003-A. The resulting cell line can overexpress the β-catenin protein, encoded by the CTNNB1 gene, after exposure to doxycycline (Dox). CTNNB1 gene expression was confirmed by quantitative PCR (qPCR) and immunofluorescence assays. Further characterization confirmed that the NERCe003-A-1 cell line expresses typical pluripotency markers and has the ability to form the three germ layers both in vitro and in vivo.
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spelling doaj.art-13b1f817c91c43d38dfbeaaf8c67d27f2022-12-21T19:05:18ZengElsevierStem Cell Research1873-50612018-04-01286165Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpressionYang Wang0Juan Yu1Lvjun Liu2Wen Li3Xingxiang Duan4Yingying Peng5Sicong Zeng6Qi Ouyang7Guangxiu Lu8Ge Lin9Yi Sun10Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, ChinaNational Engineering and Research Center of Human Stem Cells, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, China; Key Laboratory of Stem Cells and Reproductive Engineering, Ministry of Health, Changsha, China; Reproductive & Genetic Hospital of CITIC-Xiangya, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, China; National Engineering and Research Center of Human Stem Cells, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, China; National Engineering and Research Center of Human Stem Cells, Changsha, China; Key Laboratory of Stem Cells and Reproductive Engineering, Ministry of Health, Changsha, ChinaNational Engineering and Research Center of Human Stem Cells, Changsha, China; Key Laboratory of Stem Cells and Reproductive Engineering, Ministry of Health, Changsha, China; Reproductive & Genetic Hospital of CITIC-Xiangya, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, China; National Engineering and Research Center of Human Stem Cells, Changsha, China; Key Laboratory of Stem Cells and Reproductive Engineering, Ministry of Health, Changsha, China; Reproductive & Genetic Hospital of CITIC-Xiangya, Changsha, ChinaInstitute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, China; National Engineering and Research Center of Human Stem Cells, Changsha, China; Key Laboratory of Stem Cells and Reproductive Engineering, Ministry of Health, Changsha, China; Corresponding author at: Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha, China.The human embryonic stem cell (hESC) line NERCe003-A-1 was generated by introducing lentiviral-vector–mediated tetracycline-inducible β-catenin expression into a normal hESC line, NERCe003-A. The resulting cell line can overexpress the β-catenin protein, encoded by the CTNNB1 gene, after exposure to doxycycline (Dox). CTNNB1 gene expression was confirmed by quantitative PCR (qPCR) and immunofluorescence assays. Further characterization confirmed that the NERCe003-A-1 cell line expresses typical pluripotency markers and has the ability to form the three germ layers both in vitro and in vivo.http://www.sciencedirect.com/science/article/pii/S1873506118300266
spellingShingle Yang Wang
Juan Yu
Lvjun Liu
Wen Li
Xingxiang Duan
Yingying Peng
Sicong Zeng
Qi Ouyang
Guangxiu Lu
Ge Lin
Yi Sun
Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
Stem Cell Research
title Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
title_full Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
title_fullStr Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
title_full_unstemmed Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
title_short Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
title_sort generation of a human embryonic stem cell line nerce003 a 1 with lentivirus vector mediated inducible ctnnb1 overexpression
url http://www.sciencedirect.com/science/article/pii/S1873506118300266
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