Research Article
Flow cytometric analysis of neural stem cells in the developing and adult mouse brain
Article first published online: 27 AUG 2002
DOI: 10.1002/jnr.10339
Copyright © 2002 Wiley-Liss, Inc.
Issue
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Journal of Neuroscience Research
Special Issue: Stem Cells
Volume 69, Issue 6, pages 837–847, 15 September 2002
Additional Information
How to Cite
Murayama, A., Matsuzaki, Y., Kawaguchi, A., Shimazaki, T. and Okano, H. (2002), Flow cytometric analysis of neural stem cells in the developing and adult mouse brain. J. Neurosci. Res., 69: 837–847. doi: 10.1002/jnr.10339
Publication History
- Issue published online: 27 AUG 2002
- Article first published online: 27 AUG 2002
- Manuscript Revised: 8 MAY 2002
- Manuscript Accepted: 8 MAY 2002
- Manuscript Received: 2 APR 2002
Funded by
- Japan Science and Technology Corporation
- Ministry of Education, Science, Sports, Culture and Technology
- Ministry of Health, Labour and Welfare
- Abstract
- Article
- References
- Cited By
Keywords:
- neural stem cells;
- neurosphere;
- fluorescent activated cell sorting;
- forward scatter;
- side scatter;
- nestin-EGFP transgenic mice;
- side population;
- Notch1;
- CD24;
- peanut agglutinin
Abstract
Despite recent progress in the neural stem cell biology, their cellular characteristics have not been described well. We investigated various characteristics of neural stem cells (NSCs) in vivo during CNS development, using FACS to identify the NSCs. We first examined stage-dependent changes in the physical parameters, using forward scatter (FSC) and side scatter (SSC) profiles, of NSCs from the developing striatum, where they appear to be active throughout the life of mammals. NSCs were divided into several fractions according to their FSC/SSC profile. With development, their number decreased in the FSChigh fractions but increased in the FSClow/SSChigh fraction, whereas NSCs were significantly concentrated in the fraction containing the largest cells (about 20 μm in diameter) at any stage, which were mostly the cells with the highest nestin-enhancer activity. Furthermore, we demonstrated that, at all stages examined, the “side population” (SP), defined as the Hoechst 33342 low/negative fraction, which is known to be a stem cell-enriched population in bone marrow, was also enriched for Notch1-positive immature neural cells (about 60%) from the developing striatum. However, these immature SP cells were not detected in the large-cell fraction, however, but were concentrated instead in the FSClow/mid fractions. FACS analysis showed that SP cells from adults were included to some extent in the CD24low/PNAlow fraction, where NSCs were greatly concentrated. Collectively, the characteristics of NSCs were not uniform and changed developmentally. © 2002 Wiley-Liss, Inc.

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