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Abstract
show that enhancing integrin beta-1 signalling, by expressing a constitutively active integrin beta-1 (CA*β1) in the embryonic chick mesencephalon, enhances neurogenesis and increases the number of mitotic cells dividing away from the ventricular surface, analogous to sub-apical progenitors in mouse. Only non-integrin-expressing neighbouring cells (lacking CA*β1) contributed to the increased neurogenesis. Transcriptome analysis reveals upregulation of Wnt7a within the CA*β1 cells and upregulation of the ECM protein Decorin in the neighbouring non-expressing cells. Experiments using inhibitors in explant models and genetic knock-downs in vivo reveal an integrin-Wnt7a-Decorin pathway that promotes proliferation and differentiation of neuroepithelial cells, and identify Decorin as a novel neurogenic factor in the central nervous system.
Original language | English |
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Article number | 10354 |
Number of pages | 14 |
Journal | Nature Communications |
Volume | 7 |
DOIs | |
Publication status | Published - 3 Feb 2016 |
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Dive into the research topics of 'Integrin signalling regulates the expansion of neuroepithelial progenitors and neurogenesis via Wnt7a and Decorin'. Together they form a unique fingerprint.Projects
- 2 Finished
Profiles
-
Charles Ffrench-Constant
- Centre for Regenerative Medicine
- Edinburgh Neuroscience
- Deanery of Clinical Sciences - Visitor: Official Visitor
Person: Academic: Research Active , Affiliated Independent Researcher