: Dilated cardiomyopathy (DCM) is a common heart disorder caused by genetic and non-genetic etiologies, characterized by left ventricular dilatation and contractile dysfunction. Here, we created a human induced pluripotent stem cell line from peripheral blood mononuclear cells using non-integrating vectors from a patient carrying a heterozygous LMNA variant (c.481G > A, p.Glu161Lys, NM_170707.4). The obtained EURACi015-A line, showed the typical morphology of pluripotent cells, normal karyotype and exhibited pluripotency markers and a trilineage differentiation potential. This cell line can be successfully differentiated into cardiomyocytes and endothelial cells. This line represents a human in vitro model to study the genetic basis of DCM.
Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation / Cattelan, Giada; Sophie Frommelt, Laura; Volani, Chiara; Colliva, Andrea; Ciucci, Giulio; Paldino, Alessia; Dal Ferro, Matteo; Di Segni, Marina; Silipigni, Rosamaria; Pramstaller, Peter P; De Bortoli, Marzia; Zacchigna, Serena; Rossini, Alessandra. - In: STEM CELL RESEARCH. - ISSN 1876-7753. - 71/2023:(2023), pp. 103172."-"-103172."-". [10.1016/j.scr.2023.103172]
Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation
Sophie Frommelt, Laura;Colliva, Andrea;Paldino, Alessia;Dal Ferro, Matteo;Zacchigna, Serena;
2023-01-01
Abstract
: Dilated cardiomyopathy (DCM) is a common heart disorder caused by genetic and non-genetic etiologies, characterized by left ventricular dilatation and contractile dysfunction. Here, we created a human induced pluripotent stem cell line from peripheral blood mononuclear cells using non-integrating vectors from a patient carrying a heterozygous LMNA variant (c.481G > A, p.Glu161Lys, NM_170707.4). The obtained EURACi015-A line, showed the typical morphology of pluripotent cells, normal karyotype and exhibited pluripotency markers and a trilineage differentiation potential. This cell line can be successfully differentiated into cardiomyocytes and endothelial cells. This line represents a human in vitro model to study the genetic basis of DCM.| File | Dimensione | Formato | |
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