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Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation.
Mora, Cristina; Serzanti, Marialaura; Giacomelli, Alessio; Turco, Valentina; Marchina, Eleonora; Bertini, Valeria; Piovani, Giovanna; Savio, Giulia; Refsgaard, Lena; Olesen, Morten Salling; Cortellini, Venusia; Dell'Era, Patrizia.
Afiliação
  • Mora C; Cellular Fate Reprogramming Unit, Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Serzanti M; Cellular Fate Reprogramming Unit, Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Giacomelli A; Cellular Fate Reprogramming Unit, Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Turco V; Cellular Fate Reprogramming Unit, Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Marchina E; Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Bertini V; Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Piovani G; Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Savio G; Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
  • Refsgaard L; The Heart Centre, Rigshospitalet, Laboratory for Molecular Cardiology, Copenhagen, Denmark.
  • Olesen MS; The Heart Centre, Rigshospitalet, Laboratory for Molecular Cardiology, Copenhagen, Denmark.
  • Cortellini V; Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, Forensic Medicine Unit, University of Brescia, Brescia, Italy.
  • Dell'Era P; Cellular Fate Reprogramming Unit, Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy. Electronic address: patrizia.dellera@unibs.it.
Stem Cell Res ; 24: 29-32, 2017 10.
Article em En | MEDLINE | ID: mdl-29034891
Atrial fibrillation (AF) is the most common sustained arrhythmia associated with several cardiac risk factors, but increasing evidences indicated a genetic component. Indeed, genetic variations of the atrial specific KCNA5 gene have been identified in patients with early-onset lone AF. To investigate the molecular mechanisms underlying AF, we reprogrammed to pluripotency polymorphonucleated leukocytes isolated from the blood of a patient carrying a KCNA5 p.D322H mutation, using a commercially available non-integrating system. The generated iPSCs expressed pluripotency markers and differentiated toward cells belonging to the three embryonic germ layers. Moreover, the cells showed a normal karyotype and retained the p.D322H mutation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article