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Related Concept Videos

Neurulation01:30

Neurulation

41.6K
Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the...
41.6K

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Updated: Jun 3, 2025

Electroporation of Sliced Human Cortical Organoids for Studies of Gene Function
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Molecular and cellular dynamics of the developing human neocortex.

Li Wang1,2, Cheng Wang3,4, Juan A Moriano3,4,5

  • 1The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, CA, USA. Li.Wang@ucsf.edu.

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Summary
This summary is machine-generated.

This study maps human neocortex development, revealing gene regulatory networks and a tripotential progenitor cell type. Findings link these cells to glioblastoma and autism spectrum disorder risk.

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Genomics

Background:

  • Human neocortex development involves complex gene regulation and cellular dynamics.
  • Understanding these processes is crucial for deciphering neural differentiation and associated disorders.

Purpose of the Study:

  • To create a comprehensive atlas of gene regulatory networks in the developing human neocortex.
  • To identify progenitor cell types and their lineage relationships during neurogenesis and gliogenesis.
  • To investigate the link between developmental processes and neurological diseases like glioblastoma and autism spectrum disorder.

Main Methods:

  • Paired single-nucleus chromatin accessibility and transcriptome sequencing from 38 human neocortical samples (first trimester to adolescence).
  • Spatial transcriptomic analysis for cellular organization and communication.
  • Progenitor purification and lineage-tracing experiments.
  • Integration with genome-wide association study data.

Main Results:

  • Catalogued cell-type, age, and area-specific gene regulatory networks.
  • Identified tripotential intermediate progenitor cells (Tri-IPCs) responsible for producing neurons, oligodendrocytes, and astrocytes.
  • Observed transcriptomic similarity between glioblastoma cells and Tri-IPCs.
  • Generated a disease-risk map linking autism spectrum disorder risk to second-trimester neurons.

Conclusions:

  • The developed atlas provides insights into the molecular and cellular dynamics of human neocortex development.
  • Tripotential intermediate progenitor cells play a key role in neural and glial cell production and may be hijacked in glioblastoma.
  • Specific developmental trajectories in the neocortex are associated with neurological disease risk, such as autism spectrum disorder.