Cell types, lineage, and architecture of the germinal zone in the adult dentate gyrus

By Bettina Seri, Jose Manuel García-Verdugo, Lucía Collado-Morente, Bruce S. McEwen, Arturo Alvarez-Buylla. The Journal of comparative neurology, 2004

701 citations recorded by the source corpus.

Subfields: Cancer Research, Developmental Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/2d4ff95e303108734c00d2290d431915254ce9e7

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Citations in the corpus

The Chemokine Stromal Cell-Derived Factor-1 Regulates GABAergic Inputs to Neural Progenitors in the Postnatal Dentate Gyrus (2008, background): “Rapidly dividing neural progenitors (“transiently amplifying cells”) are derived from these stem cells by a process of asymmetric division (Seri et al., 2004).”
The Glial Nature of Embryonic and Adult Neural Stem Cells (2009, methodology): “Retroviral lineage-tracing experiments using the RCAS-TVA system (Holland & Varmus 1998) specifically to target GFAP- or Nestin-expressing cells in the SGZ indicate that radial astrocytes not only divide but also generate the neurons in the adult dentate gyrus (Seri et al. 2004).”
Sialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration. (2014, result): “As judged by expression of polySia and other markers, the pattern of dentate gyrus neurogenesis in humans (238) is comparable to the situation in rodents (435, 444) and undergoes similar qualitative and quantitative age-related changes.”
Brain tumour stem cells (2006, background): “There is a similar hierarchical neurogenetic system in the subgranular zone of rodent”
Brain micro-ecologies: neural stem cell niches in the adult mammalian brain (2008, background): “At least two populations of astrocytes have been defined in the SGZ: (i) radial astrocytes, which extend a process into the granule cell layer, are nestin-positive and divide and (ii) horizontal astrocytes, which extend basal processes under the granule cell layer, are nestin-negative and S100C (Kro”
Delayed Development of Adult-Generated Granule Cells in Dentate Gyrus (2006, methodology): “In the classification scheme of Alvarez-Buylla and colleagues (Seri et al., 2001, 2004), EGFP-labeled cells likely correspond to late D2 and D3 cells.”
Experience dictates stem cell fate in the adult hippocampus. (2011, positive): “…neurons are thought to differentiate from radial astrocyte-like neural stem cells (NSCs) via an intermediate multipotent neuronal progenitor (IP) and become integrated into existing networks (Carlén et al., 2002; Laplagne et al., 2006; Seri et al., 2004; Toni et al., 2008; van Praag et al., 2002).”
Signaling through BMPR-IA regulates quiescence and long-term activity of neural stem cells in the adult hippocampus. (2010, background): “…rarely divide whereas SOX2 + nonradial cells appear to cycle relatively more often; consequently, it has been suggested that the radial cell population constitutes a stem cell reservoir (Seri et al., 2001, 2004; Filippov et al., 2003; Fukuda et al., 2003; Kronenberg et al., 2003; Suh et al., 2007).”
Type‐2 cells as link between glial and neuronal lineage in adult hippocampal neurogenesis (2006, background): “Type-1 cells might constitute the largely quiescent population of stem cells that can replenish the pool of transiently amplifying progenitor cells (Seri et al., 2001, 2004).”
Anatomical gradients of adult neurogenesis and activity: young neurons in the ventral dentate gyrus are activated by water maze training (2009, positive): “…age but nonetheless results in the deepest portion of the granule cell layer containing a high proportion of granule cells that are young (Crespo et al., 1986; Dayer et al., 2003; Kempermann et al., 2003; Seri et al., 2004) and possess immature electrophysiological properties (Wang et al., 2000).”
Division-Coupled Astrocytic Differentiation and Age-Related Depletion of Neural Stem Cells in the Adult Hippocampus (2011, background): “…(Eckenhoff and Rakic, 1984; Encinas et al., 2006; Kempermann et al., 2004; Kosaka and Hama, 1986; Kronenberg et al., 2003; Mignone et al., 2004; Seri et al., 2004; Seri et al., 2001) have astroglial characteristics under electron and light microscopy and express some markers in common with…”
LIF and BMP signaling generate separate and discrete types of GFAP-expressing cells (2005, background): “Null mutation of the LIF receptor (LIFR) decreases the number of progenitors derived from E14 brain in vitro, and a reduction in the levels of gp130 decreases progenitor cell re-entry into cell cycle in vivo (Hatta et al., 2002; Shimazaki et al., 2001).”
In vivo fate analysis reveals the multipotent and self-renewal capacities of Sox2+ neural stem cells in the adult hippocampus. (2007, methodology): “…for radial glial cells and/or NSCs. Sox2-GFP cells colocalized with radial glial cell markers including NESTIN (Fukuda et al., 2003; Kronenberg et al., 2003; Mignone et al., 2004), GFAP (Seri et al., 2004), and BLBP (Anthony et al., 2004), particularly in their radial processes (Figures 1D–1F).”