A newly discovered neural stem cell population is generated by the optic lobe neuroepithelium during embryogenesis in Drosophila melanogaster.
Anna E HakesLeo OtsukiAndrea H BrandPublished in: Development (Cambridge, England) (2018)
Neural stem cells must balance symmetric and asymmetric cell divisions to generate a functioning brain of the correct size. In both the developing Drosophila visual system and mammalian cerebral cortex, symmetrically dividing neuroepithelial cells transform gradually into asymmetrically dividing progenitors that generate neurons and glia. As a result, it has been widely accepted that stem cells in these tissues switch from a symmetric, expansive phase of cell divisions to a later neurogenic phase of cell divisions. In the Drosophila optic lobe, this switch is thought to occur during larval development. However, we have found that neuroepithelial cells start to produce neuroblasts during embryonic development, demonstrating a much earlier role for neuroblasts in the developing visual system. These neuroblasts undergo neurogenic divisions, enter quiescence and are retained post-embryonically, together with neuroepithelial cells. Later in development, neuroepithelial cells undergo further cell divisions before transforming into larval neuroblasts. Our results demonstrate that the optic lobe neuroepithelium gives rise to neurons and glia over 60 h earlier than was thought previously.
Keyphrases
- stem cells
- induced apoptosis
- cell cycle arrest
- single cell
- cell therapy
- drosophila melanogaster
- spinal cord injury
- cell death
- spinal cord
- optical coherence tomography
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- subarachnoid hemorrhage
- functional connectivity
- bone marrow
- zika virus
- optic nerve
- cerebral ischemia
- resting state
- blood brain barrier