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Generation of three isogenic gene-edited Huntington's disease human embryonic stem cell lines with DOX-inducible NGN2 expression cassette in the AAVS1 safe locus.
Villegas, Luisana Duque; Chandrasekaran, Abinaya; Andersen, Sofie Amalie Flintholm; Nørremølle, Anne; Schmid, Benjamin; Pouladi, Mahmoud A; Freude, Kristine.
Affiliation
  • Villegas LD; Dept. of Cellular and Molecular Medicine, The Panum Institute, The Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200N, Denmark.
  • Chandrasekaran A; Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg, Denmark.
  • Andersen SAF; Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg, Denmark.
  • Nørremølle A; Dept. of Cellular and Molecular Medicine, The Panum Institute, The Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen 2200N, Denmark.
  • Schmid B; Bioneer A/S, Kogle Alle 2, 2970 Hørsholm, Denmark.
  • Pouladi MA; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.
  • Freude K; Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, 1870 Frederiksberg, Denmark. Electronic address: kkf@sund.ku.dk.
Stem Cell Res ; 77: 103408, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38569398
ABSTRACT
Neurogenin 2 (NGN2), a neuronal transcription factor, can expedite differentiation of stem cells into mature glutamatergic neurons. We have utilized an allelic series of previously published and characterized isogenic Huntington's disease (IsoHD) human embryonic stem cell lines (Ooi et al., 2019), carrying different CAG repeat lengths in the first exon of the huntingtin gene. These IsoHDs were modified using CRISPR/Cas9 to insert NGN2 under the TET-ON doxycycline inducible promoter. The resulting IsoHD-NGN2 cell lines retained pluripotency in the absence of doxycycline (DOX), and via addition of DOX to the culturing media differentiation to neurons was achieved within 14 days.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Huntington Disease / Doxycycline / Basic Helix-Loop-Helix Transcription Factors / Human Embryonic Stem Cells / Gene Editing / Nerve Tissue Proteins Limits: Humans Language: En Journal: Stem Cell Res Year: 2024 Document type: Article Affiliation country: Dinamarca

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Huntington Disease / Doxycycline / Basic Helix-Loop-Helix Transcription Factors / Human Embryonic Stem Cells / Gene Editing / Nerve Tissue Proteins Limits: Humans Language: En Journal: Stem Cell Res Year: 2024 Document type: Article Affiliation country: Dinamarca