Generation of four induced pluripotent stem cell lines from Korean patients with Huntington’s disease (IPBi001-A, IPBi002-A, IPBi003-A, IPBi004-A)

Human induced pluripotent stem cell (iPSC) lines were generated from peripheral blood mononuclear cells (PBMCs) of four Korean patients with Huntington's disease using a non-integrating Sendai virus-based reprogramming method. The iPSC lines expressed pluripotency markers, as confirmed by immunocytochemistry (OCT4, NANOG, SSEA-4) and flow cytometry (TRA-1-60, TRA-1-81, SSEA-4), and showed trilineage differentiation potential in vitro. All lines retained normal karyotypes and short tandem repeat (STR) profiles identical to parental PBMCs, with complete clearance of Sendai virus. These patient-derived iPSCs provide a valuable resource for Huntington's disease modeling, drug discovery, and efficacy evaluation.

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Publication Details

Journal
Stem Cell Research
Published
2026-03-11
DOI
https://doi.org/10.1016/j.scr.2026.103963
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Generation of four induced pluripotent stem cell lines from Korean patients with Huntington’s disease (IPBi001-A, IPBi002-A, IPBi003-A, IPBi004-A)

Mahito Nakanishi, E. Lee, Miju Lee, Hyun Sook Kim et al.
Stem Cell Research
Pluripotent Stem Cells Research
article

Generation of four induced pluripotent stem cell lines from Korean patients with Huntington’s disease (IPBi001-A, IPBi002-A, IPBi003-A, IPBi004-A)

Mahito Nakanishi, E. Lee, Miju Lee, Hyun Sook Kim, Jihwan Song, Beom-Soo Kim, Yoon-Eun Kim, Wonjue Choi, Min Ji Lee
article en

Abstract

Human induced pluripotent stem cell (iPSC) lines were generated from peripheral blood mononuclear cells (PBMCs) of four Korean patients with Huntington's disease using a non-integrating Sendai virus-based reprogramming method. The iPSC lines expressed pluripotency markers, as confirmed by immunocytochemistry (OCT4, NANOG, SSEA-4) and flow cytometry (TRA-1-60, TRA-1-81, SSEA-4), and showed trilineage differentiation potential in vitro. All lines retained normal karyotypes and short tandem repeat (STR) profiles identical to parental PBMCs, with complete clearance of Sendai virus. These patient-derived iPSCs provide a valuable resource for Huntington's disease modeling, drug discovery, and efficacy evaluation.

Stem Cell ResearchVol. 93
Institut Pasteur Korea (KR), University of Tsukuba (JP), CHA University Bundang Medical Center (KR), CHA University (KR), NC bit (South Korea) (KR)
Openalex Percentile: Top 24%
Pluripotent Stem Cells Research
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