| Autor: |
Eichmüller OL; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria.; University of Heidelberg, Heidelberg, Germany., Corsini NS; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria., Vértesy Á; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria., Morassut I; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria., Scholl T; Department of Pediatric and Adolescent Medicine, Medical University of Vienna, Vienna, Austria., Gruber VE; Department of Pediatric and Adolescent Medicine, Medical University of Vienna, Vienna, Austria., Peer AM; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria., Chu J; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA., Novatchkova M; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria., Hainfellner JA; Department of Neurology, Medical University of Vienna, Vienna, Austria., Paredes MF; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA., Feucht M; Department of Pediatric and Adolescent Medicine, Medical University of Vienna, Vienna, Austria., Knoblich JA; Institute of Molecular Biotechnology (IMBA), Austrian Academy of Sciences, Vienna Biocenter (VBC), Vienna, Austria.; Department of Neurology, Medical University of Vienna, Vienna, Austria. |
| Abstrakt: |
Evolutionary development of the human brain is characterized by the expansion of various brain regions. Here, we show that developmental processes specific to humans are responsible for malformations of cortical development (MCDs), which result in developmental delay and epilepsy in children. We generated a human cerebral organoid model for tuberous sclerosis complex (TSC) and identified a specific neural stem cell type, caudal late interneuron progenitor (CLIP) cells. In TSC, CLIP cells over-proliferate, generating excessive interneurons, brain tumors, and cortical malformations. Epidermal growth factor receptor inhibition reduces tumor burden, identifying potential treatment options for TSC and related disorders. The identification of CLIP cells reveals the extended interneuron generation in the human brain as a vulnerability for disease. In addition, this work demonstrates that analyzing MCDs can reveal fundamental insights into human-specific aspects of brain development. |
