Dynamic Changes in the Neurogenic Potential in the Ventricular–Subventricular Zone of Common Marmoset during Postnatal Brain Development

• Published in: Cerebral cortex (New York, N.Y. 1991) N.Y. 1991), 2020-06, Vol.30 (7), p.4092-4109
• Main Authors: Akter, Mariyam, Kaneko, Naoko, Herranz-Pérez, Vicente, Nakamura, Sayuri, Oishi, Hisashi, García-Verdugo, Jose Manuel, Sawamoto, Kazunobu
• Format: Article
• Language: English
• Subjects: Animals; Brain - cytology; Brain - growth & development; Callithrix; Cell Movement; Cell Proliferation; Cerebral Ventricles - cytology; Cerebral Ventricles - growth & development; Hippocampus - cytology; Hippocampus - growth & development; Lateral Ventricles - cytology; Lateral Ventricles - growth & development; Neocortex - cytology; Neocortex - growth & development; Neural Stem Cells - cytology; Neurogenesis; Olfactory Bulb - cytology; Olfactory Bulb - growth & development; Spatio-Temporal Analysis
• ISSN: 1047-3211; 1460-2199
• DOI: 10.1093/cercor/bhaa031

Abstract Even after birth, neuronal production continues in the ventricular–subventricular zone (V–SVZ) and hippocampus in many mammals. The immature new neurons (“neuroblasts”) migrate and then mature at their final destination. In humans, neuroblast production and migration toward the neocortex and the olfactory bulb (OB) occur actively only for a few months after birth and then sharply decline with age. However, the precise spatiotemporal profiles and fates of postnatally born neurons remain unclear due to methodological limitations. We previously found that common marmosets, small nonhuman primates, share many features of V–SVZ organization with humans. Here, using marmosets injected with thymidine analogue(s) during various postnatal periods, we demonstrated spatiotemporal changes in neurogenesis during development. V–SVZ progenitor proliferation and neuroblast migration toward the OB and neocortex sharply decreased by 4 months, most strikingly in a V–SVZ subregion from which neuroblasts migrated toward the neocortex. Postnatally born neurons matured within a few months in the OB and hippocampus but remained immature until 6 months in the neocortex. While neurogenic activity was sustained for a month after birth, the distribution and/or differentiation diversity was more restricted in 1-month-born cells than in the neonatal-born population. These findings shed light on distinctive features of postnatal neurogenesis in primates.