Neuron
ArticleCerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro
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Glial Cells
2018, Comprehensive Toxicology: Third EditionCell division mode change mediates the regulation of cerebellar granule neurogenesis controlled by the sonic hedgehog signaling
2015, Stem Cell ReportsCitation Excerpt :During the first 2–3 postnatal weeks, GNPs differentiate, exit the cell cycle, and migrate inward to form the internal granule layer, with EGL disappearing in parallel gradually. The spatiotemporal steps of proliferation and differentiation of GNPs have been described in our previous work (Gao et al., 1991; Gao and Hatten, 1993). Recent studies have demonstrated that sonic hedgehog (SHH) secreted by Purkinje cells can regulate the proliferation of GNPs (Wechsler-Reya and Scott, 1999).
Time-lapse analysis of tangential migration in Sema6A and PlexinA2 knockouts
2014, Molecular and Cellular NeuroscienceCitation Excerpt :Many in vitro assays have been previously used to study the migration of granule cells. Isolated GCs purified from postnatal brain, migrate tangentially when plated on a substrate of extracellular matrix proteins or cultured in Boyden chambers (Borghesani et al., 2002; Gao et al., 1991; Lu et al., 2001). This is also the case with EGL explants from postnatal cerebellum plated on various substrates (Kerjan et al., 2005; Nagata and Nakatsuji, 1990; Renaud et al., 2008).
PCSK9 reduces the protein levels of the LDL receptor in mouse brain during development and after ischemic stroke
2011, Journal of Lipid ResearchCitation Excerpt :Nissl staining revealed a normal cerebellum organization in Pcsk9−/− mice, with no gross modification of the EGL, molecular layer (ML), or internal granular cell layer (IGL) (Fig. 2D). This was confirmed by the staining of Purkinje cells with calbindin (supplemental Fig. IA), and of granular cells with anti-Pax-6 and anti-TAG-1, which label the granular cell bodies (24) and axons (25), respectively (supplemental Fig. IB). Although PCSK9 induces ex vivo the recruitment of undifferentiated neural progenitor cells into the neuronal lineage (1), we demonstrated that in vivo the protein levels of markers of cell proliferation (PCNA, Cyclin E), cell differentiation (Calbindin), and synapse (synaptophysin, GAP43) remain unchanged in Pcsk9−/− mice (supplemental Fig. II).
Glial Cells
2010, Comprehensive Toxicology, Second Edition