Impaired differentiation of human induced neural stem cells by TOR1A overexpression
Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-241177
- DYT-TOR1A is the most common inherited dystonia caused by a three nucleotide (GAG) deletion (dE) in the TOR1A gene. Death early after birth and cortical anomalies of the full knockout in rodents underscore its developmental importance. We therefore explored the timed effects of TOR1A-wt and TOR1A-dE during differentiation in a human neural in vitro model. We used lentiviral tet-ON expression of TOR1A-wt and -dE in induced neural stem cells derived from healthy donors. Overexpression was induced during proliferation of neural precursors, duringDYT-TOR1A is the most common inherited dystonia caused by a three nucleotide (GAG) deletion (dE) in the TOR1A gene. Death early after birth and cortical anomalies of the full knockout in rodents underscore its developmental importance. We therefore explored the timed effects of TOR1A-wt and TOR1A-dE during differentiation in a human neural in vitro model. We used lentiviral tet-ON expression of TOR1A-wt and -dE in induced neural stem cells derived from healthy donors. Overexpression was induced during proliferation of neural precursors, during differentiation and after differentiation into mature neurons. Overexpression of both wildtype and mutated protein had no effect on the viability and cell number of neural precursors as well as mature neurons when initiated before or after differentiation. However, if induced during differentiation, overexpression of TOR1A-wt and -dE led to a pronounced reduction of mature neurons in a dose dependent manner. Our data underscores the importance of physiological expression levels of TOR1A as crucial for proper neuronal differentiation. We did not find evidence for a specific impact of the mutated TOR1A on neuronal maturation.…
Autor(en): | Felix Stengel, Franca Vulinovic, Britta Meier, Karen Grütz, Christine Klein, Philipp Capetian |
---|---|
URN: | urn:nbn:de:bvb:20-opus-241177 |
Dokumentart: | Artikel / Aufsatz in einer Zeitschrift |
Institute der Universität: | Medizinische Fakultät / Neurologische Klinik und Poliklinik |
Sprache der Veröffentlichung: | Englisch |
Titel des übergeordneten Werkes / der Zeitschrift (Englisch): | Molecular Biology Reports |
Erscheinungsjahr: | 2020 |
Band / Jahrgang: | 47 |
Seitenangabe: | 3993–4001 |
Originalveröffentlichung / Quelle: | Molecular Biology Reports 47, 3993–4001 (2020). https://doi.org/10.1007/s11033-020-05390-x |
URL der Erstveröffentlichung: | https://doi.org/10.1007/s11033-020-05390-x |
DOI: | https://doi.org/10.25972/OPUS-24117 |
Allgemeine fachliche Zuordnung (DDC-Klassifikation): | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
Freie Schlagwort(e): | DYT1; TOR1A; dystonia; inducible expression; neuronal differentiation; neuronal stem cells; torsinA |
Datum der Freischaltung: | 05.07.2021 |
Lizenz (Deutsch): | CC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International |