Neurogenesis and neuronal migration in the postnatal ventricular-subventricular zone: Similarities and dissimilarities between rodents and primates

被引:20
作者
Akter, Mariya [1 ,2 ]
Kaneko, Naoko [1 ,3 ]
Sawamoto, Kazunobu [1 ,3 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Inst Brain Sci, Dept Dev & Regenerat Neurobiol,Mizuho Ku, 1 Kawasumi,Mizuho Cho, Nagoya, Aichi 4678601, Japan
[2] Noakhali Sci & Technol Univ, Dept Pharm, Noakhali 3814, Bangladesh
[3] Natl Inst Nat Sci, Natl Inst Physiol Sci, Div Neural Dev & Regenerat, 5-1 Higashiyama, Okazaki, Aichi 4448787, Japan
基金
日本学术振兴会;
关键词
Neuroblasts; Neural stem cells; Neurogenesis; Neuronal migration; Rodent; Primate; Ventricular-subventricular zone; NEURAL STEM-CELLS; ADULT NEUROGENESIS; CELLULAR COMPOSITION; FUNCTIONAL RECOVERY; GENERATION; BRAIN; ORGANIZATION; INTERNEURONS; NEUROBLASTS; MECHANISMS;
D O I
10.1016/j.neures.2020.06.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ventricular-subventricular zone (V-SVZ) is located in the walls of the lateral ventricles and pro-duces new neurons in the postnatal brain of mammals, including humans. Immature new neurons called "neuroblasts" generated by neural stem cells in the V-SVZ migrate toward their final destinations and contribute to brain development and plasticity. In this review, we describe recent progress in under-standing the similarities and dissimilarities in postnatal neurogenesis and neuronal migration between rodents and primates. In rodents, most new V-SVZ-derived neurons migrate along the rostral migratory stream towards the olfactory bulb, where they differentiate into interneurons. In contrast, in humans, the extensive migration of new neurons towards the neocortex continues for several months after birth and might be involved in the development of the expanded neocortex. The mode of migration and the fate of neuroblasts seem to change depending on their environment, destination, and roles in the brain. A better understanding of these similarities and differences between rodents and primates will help translate important findings from animal models and may contribute to the development of clinical strategies for brain repair. (c) 2020 Elsevier B.V. and Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:64 / 69
页数:6
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