Neuron
ArticleEmbryonic expression of myelin genes: Evidence for a focal source of oligodendrocyte precursors in the ventricular zone of the neural tube
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2018, BiomaterialsCitation Excerpt :Myelin P0 protein was used to examine if myelinating SC contributed to repair in our 12-week study, with nerve roots positive controls (Fig. 5A, D) [92,93]. To additionally assess residual white matter, coronal sections were co-labelled for oligodendrocytes using CNPase antibodies [92,94–96]. We observed substantial P0 staining of 50–100 μm linear segments interspersed with CNPase [97], consistent with segmental SC remyelination of peri-epicenter axons (Fig. 5A and B) as we have previously shown in one chronic human SCI [98] and is commonly observed in multiple sclerosis [99].
Expression profiles of inka2 in the murine nervous system
2015, Gene Expression PatternsCitation Excerpt :The generation of OLPs is regulated along the dorsoventral and rostrocaudal axis of the neural tube during the mid-late embryonic period. Previous studies using OLP markers such as Nkx2.2, Olig2, Sox10, and PDGFRα provided evidence of specialized oligodendrogenic regions in the ventral VZ of the embryonic forebrain, hindbrain, and spinal cord (de Castro et al., 2013; Rowitch, 2004; Tekki-Kessaris et al., 2001; Vallstedt et al., 2005; Xu et al., 2000; Yu et al., 1994; Zhou and Anderson, 2002; Zhou et al., 2001). For example, the pMN domain of the ventral VZ, which flanks the floor plate, is a major source of OLPs in the embryonic spinal cord (Zhou and Anderson, 2002), and begins to generate OLPs around E13 in mice.
Oligodendrocyte morphometry and expression of myelin - Related mRNA in ventral prefrontal white matter in major depressive disorder
2015, Journal of Psychiatric ResearchTemporal oligodendrocyte lineage progression: In vitro models of proliferation, differentiation and myelination
2014, Biochimica et Biophysica Acta - Molecular Cell ResearchCitation Excerpt :During the differentiation process, OPC give rise to preoligodendrocytes that extend multipolar short processes and start to express OPC markers as well as the sulfatide recognized by the O4 antibody [12] and the GPR17 protein [13], which persist until the immature OL stage. Upon loss of A2B5 and NG2 markers, immature OL continue to express O4 and begin to express galactocerebroside C [14]. At this point, OL become post-mitotic cells with long ramified branches and are committed to the oligodendroglial lineage [15,16].