{"title":"19神经递质对成人神经发生的调控","authors":"M. Jang, Hongjun Song, G. Ming","doi":"10.1101/087969784.52.397","DOIUrl":null,"url":null,"abstract":"Active adult neurogenesis occurs from neuronal progenitor cells (NPCs) in discrete regions of the adult mammalian central nervous system (CNS) (Abrous et al. 2005; Ming and Song 2005; Lledo et al. 2006). The generation of nascent neurons from NPCs in the intact adult CNS is restricted to the subventricular zone (SVZ) of the lateral ventricle and the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG) (Alvarez-Buylla and Lim 2004). Outside of these two regions, proliferating NPCs normally generate only glia cells, but they appear to be able to give rise to neurons after insults (Emsley et al. 2005). Accumulative evidence suggests that continuous neuronal production in the adult brain under physiological conditions is involved in specific brain functions, such as olfaction, learning, and memory (Kempermann et al. 2004a). On the other hand, neural production of NPCs under pathological conditions may contribute to brain repair (Emsley et al. 2005). Functional integration of nascent neurons is achieved by progression through sequential developmental steps that resemble embryonic and fetal neurogenesis, from proliferation and fate specification of NPCs, to differentiation, migration, axonal/dendritic development, and synaptic integration of newborn neurons (Ming and Song 2005). In contrast to developing neurogenesis, adult neurogenesis arises from a significantly different environment and proceeds with concurrent activities of mature neurons within the existing circuit. Adult neurogenesis, a striking form of structural plasticity in the intact adult CNS, is dynamically regulated by many physiological and pathological stimuli (Abrous et al. 2005; Ming and Song 2005). For example, environmental enrichment (Kempermann...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"26 1","pages":"397-423"},"PeriodicalIF":0.0000,"publicationDate":"2008-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":"{\"title\":\"19 Regulation of Adult Neurogenesis by Neurotransmitters\",\"authors\":\"M. Jang, Hongjun Song, G. Ming\",\"doi\":\"10.1101/087969784.52.397\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Active adult neurogenesis occurs from neuronal progenitor cells (NPCs) in discrete regions of the adult mammalian central nervous system (CNS) (Abrous et al. 2005; Ming and Song 2005; Lledo et al. 2006). The generation of nascent neurons from NPCs in the intact adult CNS is restricted to the subventricular zone (SVZ) of the lateral ventricle and the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG) (Alvarez-Buylla and Lim 2004). Outside of these two regions, proliferating NPCs normally generate only glia cells, but they appear to be able to give rise to neurons after insults (Emsley et al. 2005). Accumulative evidence suggests that continuous neuronal production in the adult brain under physiological conditions is involved in specific brain functions, such as olfaction, learning, and memory (Kempermann et al. 2004a). On the other hand, neural production of NPCs under pathological conditions may contribute to brain repair (Emsley et al. 2005). Functional integration of nascent neurons is achieved by progression through sequential developmental steps that resemble embryonic and fetal neurogenesis, from proliferation and fate specification of NPCs, to differentiation, migration, axonal/dendritic development, and synaptic integration of newborn neurons (Ming and Song 2005). In contrast to developing neurogenesis, adult neurogenesis arises from a significantly different environment and proceeds with concurrent activities of mature neurons within the existing circuit. Adult neurogenesis, a striking form of structural plasticity in the intact adult CNS, is dynamically regulated by many physiological and pathological stimuli (Abrous et al. 2005; Ming and Song 2005). 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引用次数: 15
摘要
成年哺乳动物中枢神经系统(CNS)离散区域的神经元祖细胞(npc)发生活跃的成年神经发生(Abrous et al. 2005;明宋2005;Lledo et al. 2006)。完整成人中枢神经系统中npc新生神经元的生成局限于侧脑室的室下区(SVZ)和海马齿状回(DG)的颗粒下区(SGZ) (Alvarez-Buylla and Lim 2004)。在这两个区域之外,增殖的npc通常只产生神经胶质细胞,但它们似乎能够在受到损伤后产生神经元(Emsley et al. 2005)。越来越多的证据表明,在生理条件下,成人大脑中连续的神经元产生与特定的大脑功能有关,如嗅觉、学习和记忆(Kempermann et al. 2004a)。另一方面,病理状态下NPCs的神经生成可能有助于大脑修复(Emsley et al. 2005)。新生神经元的功能整合是通过类似于胚胎和胎儿神经发生的顺序发育步骤来实现的,从npc的增殖和命运规范,到新生神经元的分化、迁移、轴突/树突发育和突触整合(Ming and Song 2005)。与发育中的神经发生相反,成人神经发生发生在一个明显不同的环境中,并且在现有回路中成熟神经元的同步活动中进行。成人神经发生是完整成人中枢神经系统结构可塑性的一种显著形式,受许多生理和病理刺激的动态调节(Abrous et al. 2005;Ming and Song 2005)。例如,环境富集(Kempermann…
19 Regulation of Adult Neurogenesis by Neurotransmitters
Active adult neurogenesis occurs from neuronal progenitor cells (NPCs) in discrete regions of the adult mammalian central nervous system (CNS) (Abrous et al. 2005; Ming and Song 2005; Lledo et al. 2006). The generation of nascent neurons from NPCs in the intact adult CNS is restricted to the subventricular zone (SVZ) of the lateral ventricle and the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG) (Alvarez-Buylla and Lim 2004). Outside of these two regions, proliferating NPCs normally generate only glia cells, but they appear to be able to give rise to neurons after insults (Emsley et al. 2005). Accumulative evidence suggests that continuous neuronal production in the adult brain under physiological conditions is involved in specific brain functions, such as olfaction, learning, and memory (Kempermann et al. 2004a). On the other hand, neural production of NPCs under pathological conditions may contribute to brain repair (Emsley et al. 2005). Functional integration of nascent neurons is achieved by progression through sequential developmental steps that resemble embryonic and fetal neurogenesis, from proliferation and fate specification of NPCs, to differentiation, migration, axonal/dendritic development, and synaptic integration of newborn neurons (Ming and Song 2005). In contrast to developing neurogenesis, adult neurogenesis arises from a significantly different environment and proceeds with concurrent activities of mature neurons within the existing circuit. Adult neurogenesis, a striking form of structural plasticity in the intact adult CNS, is dynamically regulated by many physiological and pathological stimuli (Abrous et al. 2005; Ming and Song 2005). For example, environmental enrichment (Kempermann...