Abstract

During embryonic development, progenitor cells are progressively restricted in their potential to generate different neural cells. A specific progenitor cell type, the radial glial cells, divides symmetrically and then asymmetrically to produce neurons, astrocytes, oligodendrocytes, and NG2-glia in the cerebral cortex. However, the potential of individual progenitors to form glial lineages remains poorly understood. To further investigate the cell progeny of single pallial GFAP-expressing progenitors, we used the in vivo genetic lineage-tracing method, the UbC-(GFAP-PB)-StarTrack. After targeting those progenitors in embryonic mice brains, we tracked their adult glial progeny in lower cortical layers. Clonal analyses revealed the presence of clones containing sibling cells of either a glial cell type (uniform clones) or two different glial cell types (mixed clones). Further, the clonal size and rostro-caudal cell dispersion of sibling cells differed depending on the cell type. We concluded that pallial E14 neural progenitors are a heterogeneous cell population with respect to which glial cell type they produce, as well as the clonal size of their cell progeny.

Highlights

  • ObjectivesConsidering that our aim is to analyze the complete cell progeny from GFAP+

  • We demonstrate the existence of adult glial clones containing sibling cells of either one glial cell type or from two different glial cell types, many of them just produce a single glial subtype

  • Most NG2-glia clones were restricted to the lower layers, while some astroglial and oligodendroglial clones spread into the upper layers and corpus callosum (CC), respectively

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Summary

Objectives

Considering that our aim is to analyze the complete cell progeny from GFAP+

Methods
Results
Conclusion
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