Lake-front property: a unique germinal niche by the lateral ventricles of the adult brain - PubMed (original) (raw)

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Lake-front property: a unique germinal niche by the lateral ventricles of the adult brain

Rebecca A Ihrie et al. Neuron. 2011.

Abstract

New neurons and glial cells are generated in an extensive germinal niche adjacent to the walls of the lateral ventricles in the adult brain. The primary progenitors (B1 cells) have astroglial characteristics but retain important neuroepithelial properties. Recent work shows how B1 cells contact all major compartments of this niche. They share the "shoreline" on the ventricles with ependymal cells, forming a unique adult ventricular zone (VZ). In the subventricular zone (SVZ), B1 cells contact transit amplifying (type C) cells, chains of young neurons (A cells), and blood vessels. How signals from these compartments influence the behavior of B1 or C cells remains largely unknown, but recent work highlights growth factors, neurotransmitters, morphogens, and the extracellular matrix as key regulators of this niche. The integration of emerging molecular and anatomical clues forecasts an exciting new understanding of how the germ of youth is actively maintained in the adult brain.

Copyright © 2011 Elsevier Inc. All rights reserved.

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Figures

Figure 1

Figure 1. The Periventricular Adult Stem Cell Niche

This illustration summarizes recent advances on our understanding of the adult VZ-SVZ niche. The apical ventricular zone is shown at top. Ependymal cells (E, in gray) are multiciliated, and the basal bodies of these cilia are oriented in the direction of cerebrospinal fluid (CSF) flow. Ependymal cells form pinwheel-like structures around the apical processes of type B1 cells (shown in blue). Type B1 cells extend a short, non-motile primary cilium into the ventricle. These cells maintain contact with the ventricle, but disassemble the primary cilium, while dividing. Type B1 cells also frequently extend a basal process with an endfoot that contacts blood vessels (Bv). Type B2 cells, in contrast, have astrocytic characteristics but do not contact the ventricle. Transit-amplifying type C cells (in green) are found close to type B cells. Dividing C cells are also often found in close proximity to blood vessels (shown at left). Type B1 cells also contact their more differentiated progeny, the chains of migrating type A neuroblasts (shown in red). Type A cells migrate tangentially in chains (shown towards right of figure) that ultimately coalesce to form the rostral migratory stream taking these young neurons to the olfactory bulb for terminal differentiation. The VZ-SVZ also includes extracellular matrix (shaded) that contacts all the cell types in this region, including blood vessels and microglia (in purple).

Figure 2

Figure 2. The Adult VZ-SVZ Niche is Patterned and Heterogeneous

A coronal section of the mouse olfactory bulb is shown at top. Neuroblasts derived from the VZ-SVZ enter at the core of the olfactory bulb (at bottom of image), then migrate radially to populate the granular layer (GRL) and glomerular layer (GCL) of the olfactory bulb. Color gradients in the mouse brain depicted at bottom indicate the sites of origin of the differently colored olfactory neurons. The ventral VZ-SVZ principally generates deep granule cells (purple) and calbindin-positive periglomerular cells (magenta). Deep granule cells typically have cell bodies close to the core of the olfactory bulb and dendritic projections that contact the inner half of the external plexiform layer (EPL), close to the mitral cell layer (ML). The dorsal SVZ, by contrast, produces superficial granule cells (green) and tyrosine hydroxylase-positive periglomerular cells (teal). Finally, the medial face of the VZ-SVZ generates calretinin-positive superficial granule cells (yellow) and periglomerular cells (orange). Note that periglomerular cells tend to be produced in more anterior regions of the VZ-SVZ, as indicated by the gradients shown in the lower image.

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