학술논문

Amplification of human interneuron progenitors promotes brain tumors and neurological defects
Document Type
article
Source
Science. 375(6579)
Subject
Cancer
Pediatric
Neurodegenerative
Rare Diseases
Stem Cell Research - Nonembryonic - Human
Tuberous Sclerosis
Epilepsy
Congenital Structural Anomalies
Stem Cell Research
Stem Cell Research - Nonembryonic - Non-Human
Neurosciences
Brain Disorders
Underpinning research
2.1 Biological and endogenous factors
Aetiology
1.1 Normal biological development and functioning
Neurological
Brain
Brain Neoplasms
Carcinogenesis
Cell Lineage
Cell Proliferation
Disease Progression
ErbB Receptors
Gene Expression Profiling
Humans
Induced Pluripotent Stem Cells
Interneurons
Loss of Heterozygosity
Neural Stem Cells
Organoids
RNA-Seq
TOR Serine-Threonine Kinases
Tuberous Sclerosis Complex 1 Protein
Tuberous Sclerosis Complex 2 Protein
General Science & Technology
Language
Abstract
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.