Chromosomal aberrations after induced pluripotent stem cells reprogramming

Detalhes bibliográficos
Autor(a) principal: Vaz,Isadora May
Data de Publicação: 2021
Outros Autores: Borgonovo,Tamara, Kasai-Brunswick,Tais Hanae, Santos,Danúbia Silva dos, Mesquita,Fernanda Cristina Paccola, Vasques,Juliana Ferreira, Gubert,Fernanda, Rebelatto,Carmen Lúcia Kuniyoshi, Senegaglia,Alexandra Cristina, Brofman,Paulo Roberto Slud
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000400103
Resumo: Abstract Induced pluripotent stem cells (iPSCs) are generated from adult cells that have been reprogrammed to pluripotency. However, in vitro cultivation and genetic reprogramming increase genetic instability, which could result in chromosomal abnormalities. Maintenance of genetic stability after reprogramming is required for possible experimental and clinical applications. The aim of this study was to analyze chromosomal alterations by using the G-banding karyotyping method applied to 97 samples from 38 iPSC cell lines generated from peripheral blood or Wharton’s jelly. Samples from patients with long QT syndrome, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis and from normal individuals revealed the following chromosomal alterations: acentric fragments, chromosomal fusions, premature centromere divisions, double minutes, radial figures, ring chromosomes, polyploidies, inversions and trisomies. An analysis of two samples generated from Wharton’s jelly before and after reprogramming showed that abnormal clones can emerge or be selected and generate an altered lineage. IPSC lines may show clonal and nonclonal chromosomal aberrations in several passages (from P6 to P34), but these aberrations are more common in later passages. Many important chromosomal aberrations were detected, showing that G-banding is very useful for evaluating genetic instability with important repercussions for the application of iPSC lines.
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spelling Chromosomal aberrations after induced pluripotent stem cells reprogrammingGenetic instabilitycytogeneticsiPSCchromosomal aberrationAbstract Induced pluripotent stem cells (iPSCs) are generated from adult cells that have been reprogrammed to pluripotency. However, in vitro cultivation and genetic reprogramming increase genetic instability, which could result in chromosomal abnormalities. Maintenance of genetic stability after reprogramming is required for possible experimental and clinical applications. The aim of this study was to analyze chromosomal alterations by using the G-banding karyotyping method applied to 97 samples from 38 iPSC cell lines generated from peripheral blood or Wharton’s jelly. Samples from patients with long QT syndrome, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis and from normal individuals revealed the following chromosomal alterations: acentric fragments, chromosomal fusions, premature centromere divisions, double minutes, radial figures, ring chromosomes, polyploidies, inversions and trisomies. An analysis of two samples generated from Wharton’s jelly before and after reprogramming showed that abnormal clones can emerge or be selected and generate an altered lineage. IPSC lines may show clonal and nonclonal chromosomal aberrations in several passages (from P6 to P34), but these aberrations are more common in later passages. Many important chromosomal aberrations were detected, showing that G-banding is very useful for evaluating genetic instability with important repercussions for the application of iPSC lines.Sociedade Brasileira de Genética2021-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000400103Genetics and Molecular Biology v.44 n.3 2021reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/1678-4685-gmb-2020-0147info:eu-repo/semantics/openAccessVaz,Isadora MayBorgonovo,TamaraKasai-Brunswick,Tais HanaeSantos,Danúbia Silva dosMesquita,Fernanda Cristina PaccolaVasques,Juliana FerreiraGubert,FernandaRebelatto,Carmen Lúcia KuniyoshiSenegaglia,Alexandra CristinaBrofman,Paulo Roberto Sludeng2021-09-01T00:00:00Zoai:scielo:S1415-47572021000400103Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2021-09-01T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.fl_str_mv Chromosomal aberrations after induced pluripotent stem cells reprogramming
title Chromosomal aberrations after induced pluripotent stem cells reprogramming
spellingShingle Chromosomal aberrations after induced pluripotent stem cells reprogramming
Vaz,Isadora May
Genetic instability
cytogenetics
iPSC
chromosomal aberration
title_short Chromosomal aberrations after induced pluripotent stem cells reprogramming
title_full Chromosomal aberrations after induced pluripotent stem cells reprogramming
title_fullStr Chromosomal aberrations after induced pluripotent stem cells reprogramming
title_full_unstemmed Chromosomal aberrations after induced pluripotent stem cells reprogramming
title_sort Chromosomal aberrations after induced pluripotent stem cells reprogramming
author Vaz,Isadora May
author_facet Vaz,Isadora May
Borgonovo,Tamara
Kasai-Brunswick,Tais Hanae
Santos,Danúbia Silva dos
Mesquita,Fernanda Cristina Paccola
Vasques,Juliana Ferreira
Gubert,Fernanda
Rebelatto,Carmen Lúcia Kuniyoshi
Senegaglia,Alexandra Cristina
Brofman,Paulo Roberto Slud
author_role author
author2 Borgonovo,Tamara
Kasai-Brunswick,Tais Hanae
Santos,Danúbia Silva dos
Mesquita,Fernanda Cristina Paccola
Vasques,Juliana Ferreira
Gubert,Fernanda
Rebelatto,Carmen Lúcia Kuniyoshi
Senegaglia,Alexandra Cristina
Brofman,Paulo Roberto Slud
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Vaz,Isadora May
Borgonovo,Tamara
Kasai-Brunswick,Tais Hanae
Santos,Danúbia Silva dos
Mesquita,Fernanda Cristina Paccola
Vasques,Juliana Ferreira
Gubert,Fernanda
Rebelatto,Carmen Lúcia Kuniyoshi
Senegaglia,Alexandra Cristina
Brofman,Paulo Roberto Slud
dc.subject.por.fl_str_mv Genetic instability
cytogenetics
iPSC
chromosomal aberration
topic Genetic instability
cytogenetics
iPSC
chromosomal aberration
description Abstract Induced pluripotent stem cells (iPSCs) are generated from adult cells that have been reprogrammed to pluripotency. However, in vitro cultivation and genetic reprogramming increase genetic instability, which could result in chromosomal abnormalities. Maintenance of genetic stability after reprogramming is required for possible experimental and clinical applications. The aim of this study was to analyze chromosomal alterations by using the G-banding karyotyping method applied to 97 samples from 38 iPSC cell lines generated from peripheral blood or Wharton’s jelly. Samples from patients with long QT syndrome, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis and from normal individuals revealed the following chromosomal alterations: acentric fragments, chromosomal fusions, premature centromere divisions, double minutes, radial figures, ring chromosomes, polyploidies, inversions and trisomies. An analysis of two samples generated from Wharton’s jelly before and after reprogramming showed that abnormal clones can emerge or be selected and generate an altered lineage. IPSC lines may show clonal and nonclonal chromosomal aberrations in several passages (from P6 to P34), but these aberrations are more common in later passages. Many important chromosomal aberrations were detected, showing that G-banding is very useful for evaluating genetic instability with important repercussions for the application of iPSC lines.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000400103
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000400103
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-4685-gmb-2020-0147
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.44 n.3 2021
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
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collection Genetics and Molecular Biology
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