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PMID: 15879324 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Enriched environment increases neural stem/progenitor cell proliferation and neurogenesis in the subventricular zone of stroke-lesioned adult rats.

Stroke ·Vol. 36 ·No. 6 ·2005-06-00 ·Pages 1278-82

Komitova M, Mattsson B, Johansson BB, Eriksson PS

Abstract

The subventricular zone in the adult brain is identified as an endogenous resource of neuronal precursors that can be recruited to adjacent lesioned areas. The hypothesis was tested that postischemic environmental enrichment might enhance subventricular zone cell genesis. A cortical infarct was induced in adult spontaneously hypertensive rats by ligating the middle cerebral artery distal to the striatal branches, after which animals were housed in either standard or enriched environment and allowed to survive for 5 weeks. The thymidine analogue bromodeoxyuridine was administered during the first postischemic week. The generation of neural stem/progenitor cells and neuronal precursors in the subventricular zone were studied with cell specific markers such as Ki67 and phosphorylated histone H3 (cell proliferation), Sox-2 (neural stem/progenitor cells), bromodeoxyuridine (slowly cycling, nonmigratory putative neural stem cells), and doublecortin (newborn immature neurons). Proliferating cells in the subventricular zone were identified as chiefly neural progenitors but also putative neural stem cells and neuronal precursors. Five weeks after stroke, proliferation in the subventricular zone was lower in stroke-lesioned rats housed in standard environment compared with nonlesioned rats. Postischemic environmental enrichment normalized cell proliferation levels, increased the numbers of putative neural stem cells as assessed with bromodeoxyuridine, and increased doublecortin-positive neuroblasts, which extended in migratory chains toward the infarct. Enriched environment increased the neural stem/progenitor cell pool and neurogenesis in the adult subventricular zone 5 weeks after a cortical stroke. This might be of potential importance for tissue regeneration.

MeSH Terms
Animals Behavior, Animal Biomarkers Brain/metabolism,pathology Brain Ischemia/metabolism,pathology Bromodeoxyuridine/pharmacology Cell Proliferation DNA-Binding Proteins/metabolism Doublecortin Domain Proteins Doublecortin Protein HMGB Proteins/metabolism Histones/metabolism Immunohistochemistry Ki-67 Antigen/biosynthesis Male Microtubule-Associated Proteins/metabolism Middle Cerebral Artery/pathology Nervous System/pathology Neurons/metabolism,pathology Neuropeptides/metabolism Phenotype Rats Rats, Inbred SHR Regeneration SOXB1 Transcription Factors Stem Cells/cytology,metabolism Stroke/pathology Thymidine/chemistry Time Factors Transcription Factors/metabolism
Chemicals
Biomarkers DNA-Binding Proteins Dcx protein, rat Doublecortin Domain Proteins Doublecortin Protein HMGB Proteins Histones Ki-67 Antigen Microtubule-Associated Proteins Neuropeptides SOXB1 Transcription Factors Sox2 protein, rat Transcription Factors Bromodeoxyuridine Thymidine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Komitova Mila
Arvid Carlsson Institute, Institute of Clinical Neuroscience, Göteborg University, Göteborg, Sweden. mila.komitova@neuro.gu.se
Mattsson Bengt
Johansson Barbro B
Eriksson Peter S
Article Info
Journal
Stroke
Abbr.
Stroke
ISSN
1524-4628
Published
2005-06-00
Epub
2005-00-05
Pages
1278-82
Language
English
Region
United States
NLM ID
0235266
Subset
IM
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