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Tissue-Specific Stem Cells
Adenomatous Polyposis Coli Is Essential for Both Neuronal Differentiation and Maintenance of Adult Neural Stem Cells in Subventricular Zone and Hippocampus†‡§
Article first published online: 18 NOV 2010
DOI: 10.1002/stem.524
Copyright © 2010 AlphaMed Press
Additional Information
How to Cite
Imura, T., Wang, X., Noda, T., Sofroniew, M. V. and Fushiki, S. (2010), Adenomatous Polyposis Coli Is Essential for Both Neuronal Differentiation and Maintenance of Adult Neural Stem Cells in Subventricular Zone and Hippocampus. STEM CELLS, 28: 2053–2064. doi: 10.1002/stem.524
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Author contributions: T.I.: conception and design, financial support, collection and/or assembly of data, data analysis and interpretation, manuscript writing, final approval of manuscript; X.W.: collection and/or assembly of data, data analysis and interpretation, final approval of manuscript; T.N.: provision of study material or patients, final approval of manuscript; M.V.S.: provision of study material or patients, data analysis and interpretation, manuscript writing, final approval of manuscript; S.F.: financial support, administrative support, data analysis and interpretation, manuscript writing, final approval of manuscript. T.I. and X.W. contributed equally to this article.
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First published online in STEM CELLS EXPRESS September 15, 2010.
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Disclosure of potential conflicts of interest is found at the end of this article.
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Telephone: 81-75-251-5849; Fax: 81-75-251-5849
Publication History
- Issue published online: 18 NOV 2010
- Article first published online: 18 NOV 2010
- Accepted manuscript online: 15 SEP 2010 01:49PM EST
- Manuscript Accepted: 2 SEP 2010
- Manuscript Received: 17 JUN 2010
Funded by
- Ministry of Education, Culture, Sports, Science and Technology of Japan. Grant Number: 18500245
- Rotary Yoneyama Memorial Foundation
- National Institutes of Health, USA, NINDS. Grant Number: NS057624
- Abstract
- Article
- References
- Supporting Information
- Cited By
Additional Supporting Information may be found in the online version of this article.
| Filename | Format | Size | Description |
|---|---|---|---|
| STEM_524_sm_suppinfoFig.eps | 13187K | Figure 1. Non-CNS phenotypes of APC-CKO mice. A. Region-specific Cre-dependent deletion of the APC gene. The PCR analysis shows that only the undeleted alleles (314 bp) were amplified from the genomic DNA of APC580S/580S brain, CKO tail, and CKO liver, whereas both the undeleted and deleted alleles (258 bp) were amplified from that of CKO brain. B. Kaplan-Meier cumulative survival rate of CKO mice (n=37) and their control littermates (n=58). The mortality rate of CKO mice was significantly higher than that of littermate controls (Ctrl) (p<0.001, Mantel-Cox log-rank test). C. Postnatal growth retardation in CKO mice. A representative picture shows a littermate control mouse, a CKO mouse with mild growth retardation (CKO1), and that with severe growth retardation (CKO2). Body weights of CKO mice were significantly smaller than those of controls (*p<0.01 and **p<0.001 versus controls, t test). D. CKO mice with juvenile lethality exhibit hemorrhagic enteritis. Note hemorrhage in the jejunoileal segment (arrowhead). HE stained section shows erosion and inflammatory cell infiltration. E. Impaired lens development in CKO mice. A representative picture demonstrates a small eye phenotype in CKO mice. HE stained sections show that lens is small and disorganized whereas retinal layers are well preserved. Scale bars: D, E, 100 ?m. HE, hematoxylin | |
| STEM_524_sm_suppinfo.doc | 34K | Supporting Information |
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