Journal Article DZNE-2020-05393

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p27kip1 Is Required for Functionally Relevant Adult Hippocampal Neurogenesis in Mice.

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2017
Wiley-Blackwell Hoboken, NJ

Stem cells 35(3), 787-799 () [10.1002/stem.2536]

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Abstract: We asked whether cell-cycle associated protein p27kip1 might be involved in the transition of precursor cells to postmitotic maturation in adult hippocampal neurogenesis. p27kip1 was expressed throughout the dentate gyrus with a strong nuclear expression in early postmitotic, calretinin-positive neurons and neuronally determined progenitor cells (type-3 and some type-2b), lower or absent expression in radial glia-like precursor cells (type-1) and type-2a cells and essentially no expression in granule cells. This suggested a transitory role in late proliferative and early postmitotic phases of neurogenesis. Inconsistent with a role limited to cell cycle arrest the acute stimuli, voluntary wheel running (RUN), environmental enrichment (ENR) and kainate-induced seizures increased p27kip1 expressing cells. Sequential short-term combination of RUN and ENR yielded more p27kip1 cells than either stimulus alone, indicating an additive effect. In vitro, p27kip1 was lowly expressed by proliferating precursor cells but increased upon differentiation. In p27kip1-/- mice neurogenesis was reduced in vivo, whereas the number of proliferating cells was increased. Accordingly, the microdissected dentate gyrus of p27kip1-/- mice generated more colonies in the neurosphere assay and an increased number of larger spheres with the differentiation potential unchanged. In p27kip1-/- monolayer cultures, proliferation was increased and cell cycle genes were upregulated. In the Morris water maze p27kip1-/- mice learned the task but were specifically impaired in the reversal phase explainable by the decrease in adult neurogenesis. We conclude that p27kip1 is involved in the decisive step around cell-cycle exit and plays an important role in activity-regulated and functionally relevant adult hippocampal neurogenesis. Stem Cells 2017;35:787-799.

Keyword(s): Aging: physiology (MeSH) ; Animals (MeSH) ; Behavior, Animal (MeSH) ; Biomarkers: metabolism (MeSH) ; Cell Differentiation (MeSH) ; Cell Proliferation (MeSH) ; Cyclin-Dependent Kinase Inhibitor p27: metabolism (MeSH) ; Female (MeSH) ; Hippocampus: metabolism (MeSH) ; Maze Learning (MeSH) ; Mice, Inbred C57BL (MeSH) ; Mice, Knockout (MeSH) ; Mitosis (MeSH) ; Neurogenesis (MeSH) ; Neurons: cytology (MeSH) ; Neurons: metabolism (MeSH) ; Phenotype (MeSH) ; Spatial Learning (MeSH) ; Biomarkers ; Cyclin-Dependent Kinase Inhibitor p27

Classification:

Contributing Institute(s):
  1. Technology Platform Neurobiology of Behaviour (AG Garthe)
  2. Adult Neurogenesis (AG Kempermann)
Research Program(s):
  1. 342 - Disease Mechanisms and Model Systems (POF3-342) (POF3-342)

Appears in the scientific report 2017
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Medline ; Creative Commons Attribution-NonCommercial-NoDerivs CC BY-NC-ND 4.0 ; OpenAccess ; BIOSIS Previews ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; IF >= 5 ; JCR ; SCOPUS ; Web of Science Core Collection
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Document types > Articles > Journal Article
Institute Collections > DD DZNE > DD DZNE-AG Kempermann
Institute Collections > DD DZNE > DD DZNE-AG Garthe
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http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Journal Article  ;  ;  ;
Isolation, Culture and Differentiation of Adult Hippocampal Precursor Cells.
Bio-protocol 7(21), e2603 () [10.21769/BioProtoc.2603] pmc  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS


 Record created 2020-02-18, last modified 2024-07-22


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