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      Single-Cell Analysis of Regional Differences in Adult V-SVZ Neural Stem Cell Lineages

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          SUMMARY

          The ventricular-subventricular zone (V-SVZ) harbors adult neural stem cells. V-SVZ neural stem cells exhibit features of astrocytes, have a regional identity, and depending on their location in the lateral or septal wall of the lateral ventricle, generate different types of neuronal and glial progeny. We performed large-scale single-cell RNA sequencing to provide a molecular atlas of cells from the lateral and septal adult V-SVZ of male and female mice. This revealed regional and sex differences among adult V-SVZ cells. We uncovered lineage potency bias at the single-cell level among lateral and septal wall astrocytes toward neurogenesis and oligodendrogenesis, respectively. Finally, we identified transcription factor co-expression modules marking key temporal steps in neurogenic and oligodendrocyte lineage progression. Our data suggest functionally important spatial diversity in neurogenesis and oligodendrogenesis in the adult brain and reveal molecular correlates of adult NSC dormancy and lineage specialization.

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          In Brief

          Mizrak et al. performed large-scale, single-cell RNA sequencing of the adult ventricular-subventricular zone neural stem cell niche. They identify regional differences between the lateral wall and septal wall, as well as sex differences in cell types and signaling pathways.

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          Most cited references43

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          Subventricular zone astrocytes are neural stem cells in the adult mammalian brain.

          Neural stem cells reside in the subventricular zone (SVZ) of the adult mammalian brain. This germinal region, which continually generates new neurons destined for the olfactory bulb, is composed of four cell types: migrating neuroblasts, immature precursors, astrocytes, and ependymal cells. Here we show that SVZ astrocytes, and not ependymal cells, remain labeled with proliferation markers after long survivals in adult mice. After elimination of immature precursors and neuroblasts by an antimitotic treatment, SVZ astrocytes divide to generate immature precursors and neuroblasts. Furthermore, in untreated mice, SVZ astrocytes specifically infected with a retrovirus give rise to new neurons in the olfactory bulb. Finally, we show that SVZ astrocytes give rise to cells that grow into multipotent neurospheres in vitro. We conclude that SVZ astrocytes act as neural stem cells in both the normal and regenerating brain.
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            Temporal Tracking of Microglia Activation in Neurodegeneration at Single-Cell Resolution

            SUMMARY Microglia, the tissue-resident macrophages in the brain, are damage sensors that react to nearly any perturbation, including neurodegenerative diseases such as Alzheimer’s disease (AD). Here, using single-cell RNA sequencing, we determined the transcriptome of more than 1,600 individual microglia cells isolated from the hippocampus of a mouse model of severe neurodegeneration with AD-like phenotypes and of control mice at multiple time points during progression of neurodegeneration. In this neurodegeneration model, we discovered two molecularly distinct reactive microglia phenotypes that are typified by modules of co-regulated type I and type II interferon response genes, respectively. Furthermore, our work identified previously unobserved heterogeneity in the response of microglia to neurodegeneration, discovered disease stage-specific microglia cell states, revealed the trajectory of cellular reprogramming of microglia in response to neurodegeneration, and uncovered the underlying transcriptional programs.
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              Neural stem cells confer unique pinwheel architecture to the ventricular surface in neurogenic regions of the adult brain.

              Neural stem cells (NSCs, B1 cells) are retained in the walls of the adult lateral ventricles but, unlike embryonic NSCs, are displaced from the ventricular zone (VZ) into the subventricular zone (SVZ) by ependymal cells. Apical and basal compartments, which in embryonic NSCs play essential roles in self-renewal and differentiation, are not evident in adult NSCs. Here we show that SVZ B1 cells in adult mice extend a minute apical ending to directly contact the ventricle and a long basal process ending on blood vessels. A closer look at the ventricular surface reveals a striking pinwheel organization specific to regions of adult neurogenesis. The pinwheel's core contains the apical endings of B1 cells and in its periphery two types of ependymal cells: multiciliated (E1) and a type (E2) characterized by only two cilia and extraordinarily complex basal bodies. These results reveal that adult NSCs retain fundamental epithelial properties, including apical and basal compartmentalization, significantly reshaping our understanding of this adult neurogenic niche.
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                Author and article information

                Journal
                101573691
                39703
                Cell Rep
                Cell Rep
                Cell reports
                2211-1247
                9 January 2019
                08 January 2019
                09 February 2019
                : 26
                : 2
                : 394-406.e5
                Affiliations
                [1 ]Department of Systems Biology, Columbia University Medical Center, New York, NY 10032, USA
                [2 ]Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA
                [3 ]Biozentrum, University of Basel, 4056 Basel, Switzerland
                [4 ]Sulzberger Columbia Genome Center, Columbia University Medical Center, New York, NY 10032, USA
                [5 ]Department of Biochemistry & Molecular Biophysics, Columbia University Medical Center, New York, NY 10032, USA
                [6 ]Lead Contact
                Author notes

                AUTHOR CONTRIBUTIONS

                D.M., P.A.S., and F.D. designed the study. D.M. and J.Y. performed the single-cell experiments. V.C., A.C.D., Z.C., and V.S.-V. performed RNAscope validations and immunostainings. H.M.L., P.A.S., and D.M. analyzed the data. D.M., H.M.L., V.S.-V., P.A.S., and F.D. wrote the manuscript.

                Article
                NIHMS1518264
                10.1016/j.celrep.2018.12.044
                6368857
                30625322
                69766423-9bb6-4d5c-b93a-2dfd6a909d22

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Cell biology
                Cell biology

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