A brain precursor atlas reveals the acquisition of developmental-like states in adult cerebral tumours.
Akram A HamedDaniel J KunzIbrahim El-HamamyQuang M TrinhOmar D SubedarLaura M RichardsWarren FoltzGarrett BullivantMatthaeus WareMaria C VladoiuJiao ZhangAntony M RajTrevor J PughMichael D TaylorSarah A TeichmannLincoln D SteinBenjamin David SimonsPeter B DirksPublished in: Nature communications (2022)
Human cerebral cancers are known to contain cell types resembling the varying stages of neural development. However, the basis of this association remains unclear. Here, we map the development of mouse cerebrum across the developmental time-course, from embryonic day 12.5 to postnatal day 365, performing single-cell transcriptomics on >100,000 cells. By comparing this reference atlas to single-cell data from >100 glial tumours of the adult and paediatric human cerebrum, we find that tumour cells have an expression signature that overlaps with temporally restricted, embryonic radial glial precursors (RGPs) and their immediate sublineages. Further, we demonstrate that prenatal transformation of RGPs in a genetic mouse model gives rise to adult cerebral tumours that show an embryonic/juvenile RGP identity. Together, these findings implicate the acquisition of embryonic-like states in the genesis of adult glioma, providing insight into the origins of human glioma, and identifying specific developmental cell types for therapeutic targeting.
Keyphrases
- single cell
- rna seq
- endothelial cells
- high throughput
- induced apoptosis
- mouse model
- subarachnoid hemorrhage
- induced pluripotent stem cells
- emergency department
- pluripotent stem cells
- childhood cancer
- pregnant women
- preterm infants
- cerebral ischemia
- young adults
- oxidative stress
- neuropathic pain
- mesenchymal stem cells
- machine learning
- cell death
- copy number
- cancer therapy
- spinal cord
- bone marrow
- resting state