The modern concept of neurogenesis in the adult brain is predicated on the premise that multipotent glial cells give rise to new neurons throughout life. Although extensive evidence exists indicating that this is the case, the transition from glial to neuronal phenotype remains poorly understood. A unique monolayer cellculture system was developed to induce, expose, and recapitulate the entire developmental series of events of subventricular zone (SVZ) neurogenesis. We show here, using immunophentoypic, ultrastructural, electrophysiological, and time-lapse analyses, that SVZ-derived glial fibrillary acidic protein low ͞A2B5 ؉ ͞nestin ؉ candidate founder cells undergo metamorphosis to eventually generate large numbers of fully differentiated interneuron phenotypes. A model of postnatal neurogenesis is considered in light of known embryonic events and reveals a limited developmental potential of SVZ stem͞progenitor cells, whereby ancestral cells in both embryonic and postnatal͞adult settings give rise to glia and GABAergic interneurons.adult stem cells ͉ electrophysiology ͉ in vitro ͉ neurogenesis ͉ subventricular zone A ttempts to trace the cellular source of neurogenesis in the adult CNS have recently led to the surprising conclusion that dedicated glial cells give rise to new neurons throughout life (1-5). Even though neurons and glia are both derived from the embryonic neuroepithelium, sharing common signaling pathways and downstream transcription factors during development (6), it is difficult to imagine how one major cell class in the adult brain can transpose into the other. Postnatal neurogenesis in the subventricular zone (SVZ) of rodents proceeds as a characteristic series of events, where multipotent glial cells (referred to as type-B cells) can divide to form colonies of neuroblasts (type-A cells) through a transit-amplifying cell population (type-C cells) (7). Newborn neuroblasts migrate from the SVZ through the rostral migratory stream and mature to GABAergic granule cells and periglomerular cells, which, 3-4 weeks after generation, integrate as inhibitory interneurons into the olfactory bulb of rodents (8-10). Certain features, such as nestinand glial-fibrillary acidic protein (GFAP) expression, are ascribed to the founder cells of postnatal neurogenesis (3,(11)(12)(13)(14), but their distinctive antigenic and functional profiles remain elusive. Traditional approaches for the isolation and characterization of persistent neurogenesis have relied on the in vitro neurosphere (NS) assay (15, 16) or on post hoc identification, depending on the incorporation of BrdUrd and͞or retroviral constructs to label precursors during cell division. However, neither of these methods affords the recognition of the dynamic processes involved in the maturation of individual cells en route from stem cells to fully differentiated neural phenotypes.Here, we present an alternative culture model that closely recapitulates in vivo postnatal͞adult SVZ neurogenesis, allowing us to monitor the entire sequence of hierarchical eve...