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. 2020 Sep 16;27(5):506–528. doi: 10.1177/1073858420954826

Figure 4.

Figure 4.

Meningeal neural progenitors generate parenchymal neurons and oligodendrocytes in physiological condition. (A) Schematic representation showing that immature neural progenitor cells and neuroblasts in meninges generate meningeal-derived neurons or rare oligodendrocytes in the brain parenchyma. In (B) meningeal-derived neurons (YFP+/CFP+, green and tdTomato, red) in the brain cortex of a postnatal day 30 (P30) PDGFRβ-Cre mouse (upper panel) expressing the neuronal markers NeuN and Satb2 (lower panel, arrowhead) are shown. Meningeal cells were labelled by injecting PDGFRβ-Cre P0 mice with a lentiviral vector expressing the Brainbow 1.0(L) reporter in the meninges allowing to trace the Cre expressing PDGFRβ meningeal cells (YFP+/CFP+ cells, green). tdTomato cells (red) are meningeal derived cells that do not express PDGFRβ. The upper panel shows that the meningeal cells migrated into cortical layers II to IV were mostly PDGFRβ-Cre-derived YFP+/CFP+ cells (green). In the lower panel, YFP/CFP meningeal-derived cells (green), NeuN (red), and Satb2 (blue), showing that the PDGFRβ-Cre-derived YFP+/CFP+ cells were NeuN+/Satb2+ neurons (arrows). Modified from Bifari and others (2017).