Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4

Two isogenic hiPSC lines, ZIPi013-B-1 and ZIPi013-B-2, were generated by CRISPR/Cas9-mediated indels in the TRPM4 gene of the previously published ZIPi013-B. TRPM4 belongs to the evolutionarily conserved family of transient receptor potential (TRP) channels. It is expressed ubiquitously and its acti...

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Main Authors: Undine Haferkamp, Narasimha Telugu, Kim Krieg, Wiebe Schaefer, Dennis Lam, Lars Binkle-Ladisch, Manuel A. Friese, Sebastian Diecke, Ole Pless
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506124003076
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author Undine Haferkamp
Narasimha Telugu
Kim Krieg
Wiebe Schaefer
Dennis Lam
Lars Binkle-Ladisch
Manuel A. Friese
Sebastian Diecke
Ole Pless
author_facet Undine Haferkamp
Narasimha Telugu
Kim Krieg
Wiebe Schaefer
Dennis Lam
Lars Binkle-Ladisch
Manuel A. Friese
Sebastian Diecke
Ole Pless
author_sort Undine Haferkamp
collection DOAJ
description Two isogenic hiPSC lines, ZIPi013-B-1 and ZIPi013-B-2, were generated by CRISPR/Cas9-mediated indels in the TRPM4 gene of the previously published ZIPi013-B. TRPM4 belongs to the evolutionarily conserved family of transient receptor potential (TRP) channels. It is expressed ubiquitously and its activity is regulated by intracellular calcium binding, changes in membrane potential, phosphoinositide lipids in the plasma membrane and the local concentration of cytoplasmic ATP and ADP. TRPM4 has been implicated in various diseases, including neurological and immune system disorders, cardiac diseases and cancer. Both new cell lines offer the opportunity to model human diseases and test therapeutic modalities addressing these.
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institution Kabale University
issn 1873-5061
language English
publishDate 2024-12-01
publisher Elsevier
record_format Article
series Stem Cell Research
spelling doaj-art-f15cd7cb53b64c50afe05c17fc33c3ae2024-12-13T10:57:00ZengElsevierStem Cell Research1873-50612024-12-0181103609Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4Undine Haferkamp0Narasimha Telugu1Kim Krieg2Wiebe Schaefer3Dennis Lam4Lars Binkle-Ladisch5Manuel A. Friese6Sebastian Diecke7Ole Pless8Fraunhofer Institute for Translational Medicine and Pharmacology ITPM, Discovery Research ScreeningPort, Hamburg, GermanyMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), Technology Platform Pluripotent Stem Cells, Berlin, GermanyFraunhofer Institute for Translational Medicine and Pharmacology ITPM, Discovery Research ScreeningPort, Hamburg, GermanyFraunhofer Institute for Translational Medicine and Pharmacology ITPM, Discovery Research ScreeningPort, Hamburg, GermanyFraunhofer Institute for Translational Medicine and Pharmacology ITPM, Discovery Research ScreeningPort, Hamburg, GermanyUniversity Medical Center Hamburg-Eppendorf, Institute of Neuroimmunology and Multiple Sclerosis, Hamburg, GermanyUniversity Medical Center Hamburg-Eppendorf, Institute of Neuroimmunology and Multiple Sclerosis, Hamburg, GermanyMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), Technology Platform Pluripotent Stem Cells, Berlin, GermanyFraunhofer Institute for Translational Medicine and Pharmacology ITPM, Discovery Research ScreeningPort, Hamburg, Germany; Corresponding author.Two isogenic hiPSC lines, ZIPi013-B-1 and ZIPi013-B-2, were generated by CRISPR/Cas9-mediated indels in the TRPM4 gene of the previously published ZIPi013-B. TRPM4 belongs to the evolutionarily conserved family of transient receptor potential (TRP) channels. It is expressed ubiquitously and its activity is regulated by intracellular calcium binding, changes in membrane potential, phosphoinositide lipids in the plasma membrane and the local concentration of cytoplasmic ATP and ADP. TRPM4 has been implicated in various diseases, including neurological and immune system disorders, cardiac diseases and cancer. Both new cell lines offer the opportunity to model human diseases and test therapeutic modalities addressing these.http://www.sciencedirect.com/science/article/pii/S1873506124003076
spellingShingle Undine Haferkamp
Narasimha Telugu
Kim Krieg
Wiebe Schaefer
Dennis Lam
Lars Binkle-Ladisch
Manuel A. Friese
Sebastian Diecke
Ole Pless
Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
Stem Cell Research
title Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
title_full Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
title_fullStr Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
title_full_unstemmed Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
title_short Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
title_sort generation of two isogenic human ipsc lines zipi013 b 1 zipi013 b 2 carrying a crispr cas9 mediated deletion of trpm4
url http://www.sciencedirect.com/science/article/pii/S1873506124003076
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