A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortex.
Laure CoquandClarisse Brunet AvalosAnne-Sophie MacéSarah FarcyAmandine Di CiccoMarusa LampicRyszard WimmerBetina BessièresTania Attie-BitachVincent FraisierPierre SensFabien GuimiotJean-Baptiste BraultAlexandre D BaffetPublished in: Nature cell biology (2024)
The human neocortex has undergone strong evolutionary expansion, largely due to an increased progenitor population, the basal radial glial cells. These cells are responsible for the production of a diversity of cell types, but the successive cell fate decisions taken by individual progenitors remain unknown. Here we developed a semi-automated live/fixed correlative imaging method to map basal radial glial cell division modes in early fetal tissue and cerebral organoids. Through the live analysis of hundreds of dividing progenitors, we show that basal radial glial cells undergo abundant symmetric amplifying divisions, and frequent self-consuming direct neurogenic divisions, bypassing intermediate progenitors. These direct neurogenic divisions are more abundant in the upper part of the subventricular zone. We furthermore demonstrate asymmetric Notch activation in the self-renewing daughter cells, independently of basal fibre inheritance. Our results reveal a remarkable conservation of fate decisions in cerebral organoids, supporting their value as models of early human neurogenesis.
Keyphrases
- induced apoptosis
- cell fate
- endothelial cells
- cell cycle arrest
- induced pluripotent stem cells
- single cell
- spinal cord injury
- endoplasmic reticulum stress
- oxidative stress
- gene expression
- subarachnoid hemorrhage
- neuropathic pain
- stem cells
- cell proliferation
- genome wide
- ultrasound guided
- cell therapy
- signaling pathway
- mesenchymal stem cells
- cerebral ischemia
- pluripotent stem cells