N-cadherin mediates interaction between precursor cells in the subventricular zone and regulates further differentiation
Neurogenesis and cell differentiation in the brain continues throughout life. In the subventricular zone and rostral migratory stream, precursor cells contact each other. Cell–cell interactions mediated via adhesion molecules are no doubt involved in establishing and maintaining the neurogenic abili...
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Published in | Journal of neuroscience research Vol. 87; no. 15; pp. 3331 - 3342 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
15.11.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Neurogenesis and cell differentiation in the brain continues throughout life. In the subventricular zone and rostral migratory stream, precursor cells contact each other. Cell–cell interactions mediated via adhesion molecules are no doubt involved in establishing and maintaining the neurogenic ability of these cells. Here, we demonstrate that N‐cadherin plays important roles in forming cell clusters and in regulating cell differentiation. N‐cadherin is abundantly expressed in chain migrating cells in the subventricular zone and rostral migratory stream but is down‐regulated after cells exit these regions. We also show that neurosphere formation is inhibited via suppression of N‐cadherin function and that N‐cadherin expression is decreased after induction of neurosphere differentiation. Furthermore, we demonstrate that functional blockade of N‐cadherin can enhance glial cell differentiation in explant cultures of precursors from the subventricular zone. © 2009 Wiley‐Liss, Inc. |
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Bibliography: | istex:C52E9175F02EBE5BB62F668A011341D10E1F9E04 ark:/67375/WNG-C382ZM26-6 New York State Spinal Cord Injury Trust - No. C020935 NIH - No. NS20147 New York State Spinal Cord Injury Trust - No. C016883 Japan Heart Foundation CIHR ArticleID:JNR22044 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0360-4012 1097-4547 1097-4547 |
DOI: | 10.1002/jnr.22044 |