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Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C

The phospholamban (PLN) R14del mutation is associated with arrhythmogenic right ventricular dysplasia (ARVD/C). ARVD/C is a cardiac disease characterized by arrhythmias and structural abnormalities in the right ventricle. Because PLN is a regulator of calcium release, this mutation can have deleteri...

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Autores principales: Vera, Carlos D., Manhas, Amit, Shenoy, Sushma P., Wheeler, Matthew T., Sallam, Karim, Wu, Joseph C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9476586/
https://www.ncbi.nlm.nih.gov/pubmed/35700631
http://dx.doi.org/10.1016/j.scr.2022.102834
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author Vera, Carlos D.
Manhas, Amit
Shenoy, Sushma P.
Wheeler, Matthew T.
Sallam, Karim
Wu, Joseph C.
author_facet Vera, Carlos D.
Manhas, Amit
Shenoy, Sushma P.
Wheeler, Matthew T.
Sallam, Karim
Wu, Joseph C.
author_sort Vera, Carlos D.
collection PubMed
description The phospholamban (PLN) R14del mutation is associated with arrhythmogenic right ventricular dysplasia (ARVD/C). ARVD/C is a cardiac disease characterized by arrhythmias and structural abnormalities in the right ventricle. Because PLN is a regulator of calcium release, this mutation can have deleterious effects on tissue integrity and contraction. This mutation is a trinucleotide (AGA) deletion that leads to an arginine deletion at position 14 of the PLN structure. Here we show two lines carrying this mutation with typical iPSC morphology, pluripotency, karyotype, ability to differentiate into the three germ layers in vitro, and readily availability for studying pathological mechanisms or ARVD/C.
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spelling pubmed-94765862022-09-15 Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C Vera, Carlos D. Manhas, Amit Shenoy, Sushma P. Wheeler, Matthew T. Sallam, Karim Wu, Joseph C. Stem Cell Res Article The phospholamban (PLN) R14del mutation is associated with arrhythmogenic right ventricular dysplasia (ARVD/C). ARVD/C is a cardiac disease characterized by arrhythmias and structural abnormalities in the right ventricle. Because PLN is a regulator of calcium release, this mutation can have deleterious effects on tissue integrity and contraction. This mutation is a trinucleotide (AGA) deletion that leads to an arginine deletion at position 14 of the PLN structure. Here we show two lines carrying this mutation with typical iPSC morphology, pluripotency, karyotype, ability to differentiate into the three germ layers in vitro, and readily availability for studying pathological mechanisms or ARVD/C. 2022-08 2022-06-06 /pmc/articles/PMC9476586/ /pubmed/35700631 http://dx.doi.org/10.1016/j.scr.2022.102834 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Vera, Carlos D.
Manhas, Amit
Shenoy, Sushma P.
Wheeler, Matthew T.
Sallam, Karim
Wu, Joseph C.
Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
title Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
title_full Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
title_fullStr Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
title_full_unstemmed Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
title_short Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
title_sort generation of two induced pluripotent stem cell lines carrying the phospholamban r14del mutation for modeling arvd/c
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9476586/
https://www.ncbi.nlm.nih.gov/pubmed/35700631
http://dx.doi.org/10.1016/j.scr.2022.102834
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