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Updated: May 22, 2025

One Mouse, Two Cultures: Isolation and Culture of Adult Neural Stem Cells from the Two Neurogenic Zones of Individual Mice
Published on: February 25, 2014
Protocol for culturing neurospheres from progenitor cells in the dentate gyrus of aged mouse hippocampus
Olga Vafaeva1, Poommaree Namchaiw2, Karl Murray3
1Center for Neuroscience, University of California, Davis, Davis, CA 95616, USA; Department of Pharmacology, School of Medicine, University of California, Davis, Davis, CA 95616, USA.
Abstract:
The neurosphere assay is the gold standard for assessing the proliferative and differentiation capacities of neural progenitor cells (NPCs). Here, we present a protocol for isolating, propagating, and maintaining hippocampal neurospheres from adult and aged mice and differentiating cultured NPCs into neurons and astrocytes. We describe steps for establishing a heterochronic co-culture of neurosphere-derived cells with primary neurons. Using neurospheres from old animals enables investigation of the effects of aging on the development and differentiation of newborn neurons.

