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Publication : Ank3-dependent SVZ niche assembly is required for the continued production of new neurons.

First Author  Paez-Gonzalez P Year  2011
Journal  Neuron Volume  71
Issue  1 Pages  61-75
PubMed ID  21745638 Mgi Jnum  J:174694
Mgi Id  MGI:5140637 Doi  10.1016/j.neuron.2011.05.029
Citation  Paez-Gonzalez P, et al. (2011) Ank3-Dependent SVZ Niche Assembly Is Required for the Continued Production of New Neurons. Neuron 71(1):61-75
abstractText  The rodent subventricular/subependymal zone (SVZ/SEZ) houses neural stem cells (NSCs) that generate olfactory bulb interneurons. It is unclear how the SVZ environment sustains neuronal production into adulthood. We discovered that the adapter molecule Ankyrin-3 (Ank3) is specifically upregulated in ventricular progenitors destined to become ependymal cells, but not in NSCs, and is required for SVZ niche assembly through progenitor lateral adhesion. Furthermore, we found that Ank3 expression is controlled by Foxj1, a transcriptional regulator of multicilia formation, and genetic deletion of this pathway led to complete loss of SVZ niche structure. Interestingly, radial glia continued to transition into postnatal NSCs without this niche. However, inducible deletion of Foxj1-Ank3 from mature SVZ ependyma resulted in dramatic depletion of neurogenesis. Targeting a pathway regulating ependymal organization/assembly and showing its requirement for new neuron production, our results have important implications for environmental control of adult neurogenesis and harvesting NSCs for replacement therapy.
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