Generation of a heterozygous Calsequestrin 2 F189L iPSC line (UMGi158-B) by CRISPR/Cas9 genome editing to investigate the cardiac pathophysiology of Takotsubo Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Takotsubo Syndrome (TTS) is a potentially life-threatening disease characterized by a transient left ventricular apical akinesia in response to β-adrenergic overstimulation. Since a genetic predisposition is assumed, we generated an iPSC-line carrying a p.F189L mutation in the calcium buffering protein Calsequestrin 2 (CasQ2). This missense mutation was previously discovered in a TTS patient and further described in a family with Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT). The established cell line is used to investigate the main mechanisms leading to TTS and CPVT using a patient-specific stem cell approach.

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Publication Details

Journal
Stem Cell Research
Published
2024-08-23
DOI
https://doi.org/10.1016/j.scr.2024.103538
Primary Topic
Takotsubo Cardiomyopathy and Associated Phenomena
Type
article
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article

Generation of a heterozygous Calsequestrin 2 F189L iPSC line (UMGi158-B) by CRISPR/Cas9 genome editing to investigate the cardiac pathophysiology of Takotsubo Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Daniela Hübscher, Sabine Rebs, Wiebke Maurer, Lukas Cyganek et al.
Stem Cell Research
Takotsubo Cardiomyopathy and Associated Phenomena
article

Generation of a heterozygous Calsequestrin 2 F189L iPSC line (UMGi158-B) by CRISPR/Cas9 genome editing to investigate the cardiac pathophysiology of Takotsubo Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Daniela Hübscher, Sabine Rebs, Wiebke Maurer, Lukas Cyganek, Alexandra Viktoria Busley, Katrin Streckfuß‐Bömeke, Gideon Syed Ali, Hanna Eberl, C. Zinke
article en

Abstract

Takotsubo Syndrome (TTS) is a potentially life-threatening disease characterized by a transient left ventricular apical akinesia in response to β-adrenergic overstimulation. Since a genetic predisposition is assumed, we generated an iPSC-line carrying a p.F189L mutation in the calcium buffering protein Calsequestrin 2 (CasQ2). This missense mutation was previously discovered in a TTS patient and further described in a family with Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT). The established cell line is used to investigate the main mechanisms leading to TTS and CPVT using a patient-specific stem cell approach.

Stem Cell ResearchVol. 81
University of Würzburg (DE), German Centre for Cardiovascular Research (DE), University of Göttingen (DE)
Good health and well-being
Openalex Percentile: Top 75%
Takotsubo Cardiomyopathy and Associated Phenomena
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