Spatiotemporal changes to the subventricular zone stem cell pool through aging

119Citations
Citations of this article
159Readers
Mendeley users who have this article in their library.

Abstract

Through adulthood, the rodent subventricular zone (SVZ) stem cell niche generates new olfactory bulb interneurons.Wehad previously reported that the number of new neurons produced in the SVZ declines through aging; however, age-related changes attributable specifically to the SVZ neural stem cell (NSC) population have not been fully characterized. Here, we conducted a spatiotemporal evaluation of adult SVZ NSCs. We assessed ventricle-contacting NSCs, which together with ependymal cells form regenerative units (pinwheels) along the lateral wall of the lateral ventricle. Based on their apical GFAP-expressing process, individual NSCs were identified across the ventricle surface using serial reconstruction ofthe SVZ.We observed an 86% declinein total NSCs/mm 2 of intact ependyma in 2-year old versus 3-month-old mice, with fewer NSC processes within each aged pinwheel. This resulted in an associated 78% decline in total pinwheel units/mm 2. Regional analysis along the lateral ventricle surface revealed that the age-dependent decline of NSCs and pinwheels is spatially uniform and ultimately maintains the conserved ratio of olfactory bulb interneuron subtypes generated in young mice. However, the overall neurogenic output of the aged SVZ is reduced. Surprisingly, we found no significant change in the number of actively proliferating NSCsper mm 2ofventriclesurface.Instead, ourdata reveal that, although the total NSC number,pinwheel unitsand NSCs per pinwheel decline with age, the percentage of actively, mitotic NSCs increases, indicating that age-related declines in SVZ-mediated olfactory bulb neurogenesis occur downstream of NSC proliferation. © 2012 the authors.

Cite

CITATION STYLE

APA

Shook, B. A., Manz, D. H., Peters, J. J., Kang, S., & Conover, J. C. (2012). Spatiotemporal changes to the subventricular zone stem cell pool through aging. Journal of Neuroscience, 32(20), 6947–6956. https://doi.org/10.1523/JNEUROSCI.5987-11.2012

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free