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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Format: | Article |
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Elsevier
2024-12-01
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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. |
format | Article |
id | doaj-art-f15cd7cb53b64c50afe05c17fc33c3ae |
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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