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

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作者
Villegas, Luisana Duque [1 ]
Chandrasekaran, Abinaya [2 ]
Andersen, Sofie Amalie Flintholm [2 ]
Norremolle, Anne [1 ]
Schmid, Benjamin [3 ]
Pouladi, Mahmoud A. [4 ]
Freude, Kristine [2 ]
机构
[1] Univ Copenhagen, Panum Inst, Fac Hlth & Med Sci, Dept Cellular & Mol Med, 2200N, Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Vet & Anim Sci, DK-1870 Frederiksberg, Denmark
[3] Bioneer AS, Kogle 2, DK-2970 Horsholm, Denmark
[4] Univ British Columbia, British Columbia Childrens Hosp Res Inst, Ctr Mol Med & Therapeut,Dept Med Genet, Djavad Mowafaghian Ctr Brain Hlth, Vancouver, BC, Canada
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D O I
10.1016/j.scr.2024.103408
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
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页数:6
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