AI Article Synopsis

  • Neural cell diversity is crucial for the different functions of brain regions, influenced by specific gene expression in progenitors during development.
  • Researchers have discovered that both neurons and astrocytes in the neocortex and thalamus share unique transcriptional and epigenetic signatures, highlighting a commonality in their molecular programs.
  • This shared signature not only distinguishes these cells across different brain regions but also remains present even after astrocytes are reprogrammed into neurons, which could aid in developing future brain repair techniques.

Article Abstract

Neural cell diversity is essential to endow distinct brain regions with specific functions. During development, progenitors within these regions are characterized by specific gene expression programs, contributing to the generation of diversity in postmitotic neurons and astrocytes. While the region-specific molecular diversity of neurons and astrocytes is increasingly understood, whether these cells share region-specific programs remains unknown. Here, we show that in the neocortex and thalamus, neurons and astrocytes express shared region-specific transcriptional and epigenetic signatures. These signatures not only distinguish cells across these two brain regions but are also detected across substructures within regions, such as distinct thalamic nuclei, where clonal analysis reveals the existence of common nucleus-specific progenitors for neurons and astrocytes. Consistent with their shared molecular signature, regional specificity is maintained following astrocyte-to-neuron reprogramming. A detailed understanding of these regional-specific signatures may thus inform strategies for future cell-based brain repair.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026135PMC
http://dx.doi.org/10.1126/sciadv.abe8978DOI Listing

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