{"title":"14 The Balance of Trophic Support and Cell Death in Adult Neurogenesis","authors":"H. Kuhn","doi":"10.1101/087969784.52.283","DOIUrl":null,"url":null,"abstract":"The fact that continuous proliferation of stem cells and progenitors, as well as the production of neurons, occurs in the adult CNS raises several basic questions concerning the number of neurons required in a particular system: Can we observe a continued growth of brain regions that sustain neurogenesis? Or does an elimination mechanism exist that keeps the number of cells constant? If so, are the old ones replaced or are the new neurons competing for limited network access? What signals would support their survival and integration and what factors are responsible for their elimination? This chapter addresses these and other questions regarding regulatory mechanisms affecting adult neurogenesis by controlling cell survival. ARE NEUROGENIC BRAIN REGIONS EXPANDING DESPITE SPACE LIMITATIONS? This question was initially addressed several decades ago, following the first evidence that adult mammalian neurogenesis exists. Total neuronal cell counts of the olfactory bulb (OB) and dentate gyrus (DG) at different ages revealed that in both regions, a continued growth of the granule cell layer occurs throughout adult life. From 1 month of age, when the developmental production of granule cells can be considered complete, until 1 year of age, the number of DG granule cells doubles in the rat (Bayer 1982; Bayer et al. 1982). A rise in total volume and increased cell density due to reduced cell diameter both contribute to this phenomenon. In the rat OB, a linear growth of the granule cell layer was observed with age (Kaplan et al. 1985), with the number of olfactory...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"649 1","pages":"283-298"},"PeriodicalIF":0.0000,"publicationDate":"2008-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor Monograph Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/087969784.52.283","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
The fact that continuous proliferation of stem cells and progenitors, as well as the production of neurons, occurs in the adult CNS raises several basic questions concerning the number of neurons required in a particular system: Can we observe a continued growth of brain regions that sustain neurogenesis? Or does an elimination mechanism exist that keeps the number of cells constant? If so, are the old ones replaced or are the new neurons competing for limited network access? What signals would support their survival and integration and what factors are responsible for their elimination? This chapter addresses these and other questions regarding regulatory mechanisms affecting adult neurogenesis by controlling cell survival. ARE NEUROGENIC BRAIN REGIONS EXPANDING DESPITE SPACE LIMITATIONS? This question was initially addressed several decades ago, following the first evidence that adult mammalian neurogenesis exists. Total neuronal cell counts of the olfactory bulb (OB) and dentate gyrus (DG) at different ages revealed that in both regions, a continued growth of the granule cell layer occurs throughout adult life. From 1 month of age, when the developmental production of granule cells can be considered complete, until 1 year of age, the number of DG granule cells doubles in the rat (Bayer 1982; Bayer et al. 1982). A rise in total volume and increased cell density due to reduced cell diameter both contribute to this phenomenon. In the rat OB, a linear growth of the granule cell layer was observed with age (Kaplan et al. 1985), with the number of olfactory...
干细胞和祖细胞的持续增殖,以及神经元的产生,发生在成人中枢神经系统中,这一事实提出了几个关于特定系统所需神经元数量的基本问题:我们能否观察到维持神经发生的大脑区域的持续增长?还是存在一种使细胞数量保持不变的消除机制?如果是这样,是旧的神经元被取代了,还是新的神经元在争夺有限的网络接入?什么信号会支持它们的生存和整合,什么因素会导致它们的消失?本章讨论了通过控制细胞存活来影响成人神经发生的调节机制的这些和其他问题。尽管空间有限,神经源性脑区是否仍在扩张?这个问题最初是在几十年前提出的,当时有第一个证据表明成年哺乳动物存在神经发生。嗅球(OB)和齿状回(DG)在不同年龄的总神经元细胞计数显示,在这两个区域,颗粒细胞层的持续生长发生在整个成年期。从1月龄开始,当颗粒细胞的发育产生可以被认为是完全的时候,直到1岁,大鼠的DG颗粒细胞数量增加一倍(Bayer 1982;Bayer et al. 1982)。总体积的增加和由于细胞直径减小而增加的细胞密度都有助于这种现象。在大鼠OB中,随着年龄的增长,颗粒细胞层呈线性增长(Kaplan et al. 1985),嗅觉细胞的数量增加。