Comparing Adult Hippocampal Neurogenesis Across Species: Translating Time to Predict the Tempo in Humans

被引:53
|
作者
Charvet, Christine J. [1 ,2 ]
Finlay, Barbara L. [2 ]
机构
[1] Delaware State Univ, Dept Psychol, Dover, DE USA
[2] Cornell Univ, Dept Psychol, Lab Behav & Evolutionary Neurosci, Ithaca, NY 14853 USA
来源
FRONTIERS IN NEUROSCIENCE | 2018年 / 12卷
关键词
hippocampus; neurogenesis; adult; human; rodent; monkey; Ki67; allometry; DENTATE GYRUS; CONSERVED PATTERN; BRAIN-DEVELOPMENT; NEURON NUMBER; RNA-SEQ; EVOLUTION; MOUSE; ALLOMETRY; MAMMALS; CORTEX;
D O I
10.3389/fnins.2018.00706
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Comparison of neurodevelopmental sequences between species whose initial period of brain organization may vary from 100 days to 1,000 days, and whose progress is intrinsically non-linear presents large challenges in normalization. Comparing adult timelines when lifespans stretch from 1 year to 75 years, when underlying cellular mechanisms under scrutiny do not scale similarly, presents challenges to simple detection and comparison. The question of adult hippocampal neurogenesis has generated numerous controversies regarding its simple presence or absence in humans versus rodents, whether it is best described as the tail of a distribution centered on early neural development, or is several distinct processes. In addition, adult neurogenesis may have substantially changed in evolutionary time in different taxonomic groups. Here, we extend and adapt a model of the cross-species transformation of early neurodevelopmental events which presently reaches up to the equivalent of the third human postnatal year for 18 mammalian species (www. translatingtime. net) to address questions relevant to hippocampal neurogenesis, which permit extending the database to adolescence or perhaps to the whole lifespan. We acquired quantitative data delimiting the envelope of hippocampal neurogenesis from cell cycle markers (i. e., Ki67 and DCX) and RNA sequencing data for two primates (macaque and humans) and two rodents (rat and mouse). To improve species coverage in primates, we gathered the same data from marmosets (Callithrix jacchus), but additionally gathered data on a number of developmental milestones to find equivalent developmental time points between marmosets and other species. When all species are so modeled, and represented in a common time frame, the envelopes of hippocampal neurogenesis are essentially superimposable. Early developmental events involving the olfactory and limbic system start and conclude possibly slightly early in primates than rodents, and we find a comparable early conclusion of primate hippocampal neurogenesis (as assessed by the relative number of Ki67 cells) suggesting a plateau to low levels at approximately 2 years of age in humans. Marmosets show equivalent patterns within neurodevelopment, but unlike macaque and humans may have wholesale delay in the initiation of neurodevelopment processes previously observed in some precocial mammals such as the guinea pig and multiple large ungulates.
引用
收藏
页数:18
相关论文
共 35 条
  • [1] Methods to study adult hippocampal neurogenesis in humans and across the phylogeny
    Terreros-Roncal, Julia
    Flor-Garcia, Miguel
    Moreno-Jimenez, Elena P.
    Rodriguez-Moreno, Carla B.
    Marquez-Valadez, Berenice
    Gallardo-Caballero, Marta
    Rabano, Alberto
    Llorens-Martin, Maria
    HIPPOCAMPUS, 2023, 33 (04) : 271 - 306
  • [2] Evidences for Adult Hippocampal Neurogenesis in Humans
    Moreno-Jimenez, Elena P.
    Terreros-Roncal, Julia
    Flor-Garcia, Miguel
    Rabano, Alberto
    Llorens-Martin, Maria
    JOURNAL OF NEUROSCIENCE, 2021, 41 (12): : 2541 - 2553
  • [3] Dynamics of Hippocampal Neurogenesis in Adult Humans
    Spalding, Kirsty L.
    Bergmann, Olaf
    Alkass, Kanar
    Bernard, Samuel
    Salehpour, Mehran
    Huttner, Hagen B.
    Bostrom, Emil
    Westerlund, Isabelle
    Vial, Celine
    Buchholz, Bruce A.
    Possnert, Goran
    Mash, Deborah C.
    Druid, Henrik
    Frisen, Jonas
    CELL, 2013, 153 (06) : 1219 - 1227
  • [4] Trophic Factors Involved In Developmental and Adult Hippocampal Neurogenesis In Humans
    Adle-Biassette, Homa
    Cipriani, Sara
    Ferrer, Isidre
    Nardelli, Jeannette
    Kovacs, Gabor
    Aronica, Eleonora
    Guimiot, Fabien
    Verney, Catherine
    Gressens, Pierre
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2017, 76 (06): : 522 - 522
  • [5] Modeling hippocampal neurogenesis across the lifespan in seven species
    Lazic, Stanley E.
    NEUROBIOLOGY OF AGING, 2012, 33 (08) : 1664 - 1671
  • [6] Trophic Factors Involved In Developmental and Adult Hippocampal Neurogenesis In Humans
    Adle-Biassette, Homa
    Cipriani, Sara
    Ferrer, Isidre
    Kovacs, Gabor
    Aronica, Eleonora
    Manivet, Philippe
    Gressens, Pierre
    BRAIN PATHOLOGY, 2019, 29 : 106 - 106
  • [7] A Role for Adult Hippocampal Neurogenesis at Multiple Time Scales: A Study of Recent and Remote Memory in Humans
    Dery, Nicolas
    Goldstein, Aaron
    Becker, Suzanna
    BEHAVIORAL NEUROSCIENCE, 2015, 129 (04) : 435 - 449
  • [8] Comparing adult hippocampal neurogenesis in mammalian species and orders: influence of chronological age and life history stage
    Amrein, Irmgard
    Isler, Karin
    Lipp, Hans-Peter
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2011, 34 (06) : 978 - 987
  • [9] Transcriptome dynamics of hippocampal neurogenesis in macaques across the lifespan and aged humans
    Wei Wang
    Mengdi Wang
    Meng Yang
    Bo Zeng
    Wenying Qiu
    Qiang Ma
    Xiaoxi Jing
    Qianqian Zhang
    Bosong Wang
    Chonghai Yin
    Jiyao Zhang
    Yuxin Ge
    Yufeng Lu
    Weizhi Ji
    Qian Wu
    Chao Ma
    Xiaoqun Wang
    Cell Research, 2022, 32 : 729 - 743
  • [10] Transcriptome dynamics of hippocampal neurogenesis in macaques across the lifespan and aged humans
    Wang, Wei
    Wang, Mengdi
    Yang, Meng
    Zeng, Bo
    Qiu, Wenying
    Ma, Qiang
    Jing, Xiaoxi
    Zhang, Qianqian
    Wang, Bosong
    Yin, Chonghai
    Zhang, Jiyao
    Ge, Yuxin
    Lu, Yufeng
    Ji, Weizhi
    Wu, Qian
    Ma, Chao
    Wang, Xiaoqun
    CELL RESEARCH, 2022, 32 (08) : 729 - 743