Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism

ALDH2 gene is coded for the aldehyde dehydrogenase (ALDH), which is an enzyme involved in alcohol metabolism. Compared to normal aldehyde dehydrogenases, a homozygous point mutation on exon 12 from G to A significantly reduces its efficiency. In this study, we have reported the generation of IBMS-iP...

Full description

Bibliographic Details
Main Authors: Ming-Heng Tsai, Yueh-Ting Chiu, Darien Zhing-Herr Chan, Cheng-Hao Wen, Shih-Han Syu, Huai-En Lu, Chi-Ying F. Huang, Yenn-Jiang Lin, Shih-Lin Chang, Li-Wei Lo, Ching-Ying Huang, Yu-Feng Hu, Patrick C.H. Hsieh, Shih-Ann Chen
Format: Article
Language:English
Published: Elsevier 2021-07-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506121002622
id doaj-ec7d1e9f770348e6925e2b7e39624faa
record_format Article
spelling doaj-ec7d1e9f770348e6925e2b7e39624faa2021-07-09T04:42:39ZengElsevierStem Cell Research1873-50612021-07-0154102416Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphismMing-Heng Tsai0Yueh-Ting Chiu1Darien Zhing-Herr Chan2Cheng-Hao Wen3Shih-Han Syu4Huai-En Lu5Chi-Ying F. Huang6Yenn-Jiang Lin7Shih-Lin Chang8Li-Wei Lo9Ching-Ying Huang10Yu-Feng Hu11Patrick C.H. Hsieh12Shih-Ann Chen13Institute of Biomedical Sciences, Academia Sinica, Taipei, TaiwanInstitute of Biomedical Sciences, Academia Sinica, Taipei, TaiwanInstitute of Biomedical Sciences, Academia Sinica, Taipei, TaiwanFood Industry Research and Development Institute, Hsinchu, TaiwanFood Industry Research and Development Institute, Hsinchu, TaiwanFood Industry Research and Development Institute, Hsinchu, TaiwanInstitute of Biopharmaceutical Sciences, National Yang Ming University, Taipei, TaiwanFaculty of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Heart Rhythm Center, Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, TaiwanFaculty of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Heart Rhythm Center, Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, TaiwanFaculty of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Heart Rhythm Center, Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, TaiwanInstitute of Biomedical Sciences, Academia Sinica, Taipei, TaiwanInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan; Faculty of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Heart Rhythm Center, Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan; Corresponding authors.Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan; Corresponding authors.Faculty of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Heart Rhythm Center, Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, TaiwanALDH2 gene is coded for the aldehyde dehydrogenase (ALDH), which is an enzyme involved in alcohol metabolism. Compared to normal aldehyde dehydrogenases, a homozygous point mutation on exon 12 from G to A significantly reduces its efficiency. In this study, we have reported the generation of IBMS-iPSC-021-04, IBMS-iPSC-022-01, and IBMS-iPSC-023-03 as induced pluripotent stem cell (iPSC) lines carrying the homozygous form of ALDH2 with the rs671 genetic polymorphism (E487K mutation). These cell lines were characterized in terms of pluripotency and differentiation potential. They serve as useful platforms to study alcohol metabolism and other chronic diseases associated with alcohol consumption.http://www.sciencedirect.com/science/article/pii/S1873506121002622
collection DOAJ
language English
format Article
sources DOAJ
author Ming-Heng Tsai
Yueh-Ting Chiu
Darien Zhing-Herr Chan
Cheng-Hao Wen
Shih-Han Syu
Huai-En Lu
Chi-Ying F. Huang
Yenn-Jiang Lin
Shih-Lin Chang
Li-Wei Lo
Ching-Ying Huang
Yu-Feng Hu
Patrick C.H. Hsieh
Shih-Ann Chen
spellingShingle Ming-Heng Tsai
Yueh-Ting Chiu
Darien Zhing-Herr Chan
Cheng-Hao Wen
Shih-Han Syu
Huai-En Lu
Chi-Ying F. Huang
Yenn-Jiang Lin
Shih-Lin Chang
Li-Wei Lo
Ching-Ying Huang
Yu-Feng Hu
Patrick C.H. Hsieh
Shih-Ann Chen
Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
Stem Cell Research
author_facet Ming-Heng Tsai
Yueh-Ting Chiu
Darien Zhing-Herr Chan
Cheng-Hao Wen
Shih-Han Syu
Huai-En Lu
Chi-Ying F. Huang
Yenn-Jiang Lin
Shih-Lin Chang
Li-Wei Lo
Ching-Ying Huang
Yu-Feng Hu
Patrick C.H. Hsieh
Shih-Ann Chen
author_sort Ming-Heng Tsai
title Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
title_short Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
title_full Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
title_fullStr Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
title_full_unstemmed Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
title_sort generation of ibms-ipsc-021, -022, -023 human induced pluripotent stem cells (ibmsi016-a, ibmsi017-a, and ibmsi018-a) derived from patients with the aldh2 rs671 polymorphism
publisher Elsevier
series Stem Cell Research
issn 1873-5061
publishDate 2021-07-01
description ALDH2 gene is coded for the aldehyde dehydrogenase (ALDH), which is an enzyme involved in alcohol metabolism. Compared to normal aldehyde dehydrogenases, a homozygous point mutation on exon 12 from G to A significantly reduces its efficiency. In this study, we have reported the generation of IBMS-iPSC-021-04, IBMS-iPSC-022-01, and IBMS-iPSC-023-03 as induced pluripotent stem cell (iPSC) lines carrying the homozygous form of ALDH2 with the rs671 genetic polymorphism (E487K mutation). These cell lines were characterized in terms of pluripotency and differentiation potential. They serve as useful platforms to study alcohol metabolism and other chronic diseases associated with alcohol consumption.
url http://www.sciencedirect.com/science/article/pii/S1873506121002622
work_keys_str_mv AT minghengtsai generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT yuehtingchiu generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT darienzhingherrchan generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT chenghaowen generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT shihhansyu generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT huaienlu generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT chiyingfhuang generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT yennjianglin generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT shihlinchang generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT liweilo generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT chingyinghuang generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT yufenghu generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT patrickchhsieh generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
AT shihannchen generationofibmsipsc021022023humaninducedpluripotentstemcellsibmsi016aibmsi017aandibmsi018aderivedfrompatientswiththealdh2rs671polymorphism
_version_ 1721312221446799360