Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation

PARK2 is the most common autosomal recessive form of Parkinson’s disease and is caused by mutations in parkin that result in early-onset loss of dopaminergic neurons in the substantia nigra. In this study, we established an induced pluripotent stem cell (iPSC) line from a patient harboring a homozyg...

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Main Authors: Kei-ichi Ishikawa, Ayami Okuzumi, Hiroyo Yoshino, Nobutaka Hattori, Wado Akamatsu
Format: Article
Language:English
Published: Elsevier 2024-04-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506124000217
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author Kei-ichi Ishikawa
Ayami Okuzumi
Hiroyo Yoshino
Nobutaka Hattori
Wado Akamatsu
author_facet Kei-ichi Ishikawa
Ayami Okuzumi
Hiroyo Yoshino
Nobutaka Hattori
Wado Akamatsu
author_sort Kei-ichi Ishikawa
collection DOAJ
description PARK2 is the most common autosomal recessive form of Parkinson’s disease and is caused by mutations in parkin that result in early-onset loss of dopaminergic neurons in the substantia nigra. In this study, we established an induced pluripotent stem cell (iPSC) line from a patient harboring a homozygous exon 3 deletion in PARK2. The established iPSCs showed pluripotency, the capacity to differentiate into the three germ layers, and normal karyotypes.
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spelling doaj.art-fd84481b5a3a4c56968962eb29a053922024-02-03T06:35:27ZengElsevierStem Cell Research1873-50612024-04-0176103323Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutationKei-ichi Ishikawa0Ayami Okuzumi1Hiroyo Yoshino2Nobutaka Hattori3Wado Akamatsu4Center for Genomic and Regenerative Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan; Department of Research and Development for Organoids, Juntendo University School of Medicine, Tokyo, Japan; Corresponding author.Department of Neurology, Juntendo University School of Medicine, Tokyo, JapanResearch Institute for Diseases of Old Age, Juntendo University Graduate School of Medicine, Tokyo, JapanCenter for Genomic and Regenerative Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan; Department of Research and Development for Organoids, Juntendo University School of Medicine, Tokyo, Japan; Neurodegenerative Disorders Collaborative Laboratory, RIKEN Center for Brain Science, Saitama, JapanCenter for Genomic and Regenerative Medicine, Juntendo University Graduate School of Medicine, Tokyo, JapanPARK2 is the most common autosomal recessive form of Parkinson’s disease and is caused by mutations in parkin that result in early-onset loss of dopaminergic neurons in the substantia nigra. In this study, we established an induced pluripotent stem cell (iPSC) line from a patient harboring a homozygous exon 3 deletion in PARK2. The established iPSCs showed pluripotency, the capacity to differentiate into the three germ layers, and normal karyotypes.http://www.sciencedirect.com/science/article/pii/S1873506124000217
spellingShingle Kei-ichi Ishikawa
Ayami Okuzumi
Hiroyo Yoshino
Nobutaka Hattori
Wado Akamatsu
Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation
Stem Cell Research
title Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation
title_full Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation
title_fullStr Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation
title_full_unstemmed Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation
title_short Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson’s disease with PARK2 mutation
title_sort generation of hipscs jucgrmi003 a from a patient with parkinson s disease with park2 mutation
url http://www.sciencedirect.com/science/article/pii/S1873506124000217
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