We report the generation of three isogenic iPSC clones (UNIBSi007-A, UNIBSi007-B, and UNIBSi007-C) obtained from fibroblasts of a patient with Aicardi Goutières Syndrome (AGS) carrying a homozygous mutation in RNaseH2B. Cells were transduced using a Sendai virus based system, delivering the human OCT4, SOX2, c-MYC and KLF4 transcription factors. The resulting transgene-free iPSC lines retained the disease-causing DNA mutation, showed normal karyotype, expressed pluripotent markers and could differentiate in vitro toward cells of the three embryonic germ layers.

Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B

Lanzi G.;Cereda C.;Orcesi S.;Fazzi E.;Giliani S.
2019-01-01

Abstract

We report the generation of three isogenic iPSC clones (UNIBSi007-A, UNIBSi007-B, and UNIBSi007-C) obtained from fibroblasts of a patient with Aicardi Goutières Syndrome (AGS) carrying a homozygous mutation in RNaseH2B. Cells were transduced using a Sendai virus based system, delivering the human OCT4, SOX2, c-MYC and KLF4 transcription factors. The resulting transgene-free iPSC lines retained the disease-causing DNA mutation, showed normal karyotype, expressed pluripotent markers and could differentiate in vitro toward cells of the three embryonic germ layers.
2019
Esperti anonimi
Inglese
Internazionale
STAMPA
Autoimmune Diseases of the Nervous System; Base Sequence; Cell Culture Techniques; Cell Line; Child; Female; Fibroblasts; Humans; Induced Pluripotent Stem Cells; Mutation; Nervous System Malformations; Reproducibility of Results; Ribonuclease H
https://www.sciencedirect.com/science/article/pii/S1873506119302508?via=ihub
no
13
info:eu-repo/semantics/article
262
Ferraro, R. M.; Masneri, S.; Lanzi, G.; Barisani, C.; Piovani, G.; Savio, G.; Cattalini, M.; Galli, J.; Cereda, C.; Muzi-Falconi, M.; Orcesi, S.; Fazz...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1361055
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