Existence of a potential neurogenic system in the adult human brain

被引:38
|
作者
Nogueira, Adriano Barreto [1 ,2 ]
Sogayar, Mari Cleide [3 ]
Colquhoun, Alison [4 ]
Siqueira, Sheila Aparecida [5 ]
Nogueira, Ariel Barreto [5 ]
Marchiori, Paulo Euripedes [6 ]
Teixeira, Manoel Jacobsen [1 ,2 ]
机构
[1] Univ Sao Paulo, Fac Med, Hosp Clin, Div Neurosurg Clin, BR-05403900 Sao Paulo, Brazil
[2] Univ Sao Paulo, Fac Med, Hosp Clin, Lab Expt Surg Res, BR-05403900 Sao Paulo, Brazil
[3] Univ Sao Paulo, Fac Med, Cell & Mol Therapy Ctr, BR-05403900 Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Biomed Sci, Dept Cellular & Dev Biol, BR-05403900 Sao Paulo, Brazil
[5] Univ Sao Paulo, Fac Med, Hosp Clin, Dept Pathol, BR-05403900 Sao Paulo, Brazil
[6] Univ Sao Paulo, Fac Med, Dept Neurol, BR-05403900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Neurogenic niche; Neurogenesis; Neural stem cell; Adult human brain; Limbic system; Temporal lobe; Hippocampus; Hypothalamus; Nestin; Doublecortin; NEURAL STEM-CELLS; SUBVENTRICULAR ZONE; PROGENITOR CELLS; DENTATE GYRUS; TEMPORAL-LOBE; STEM/PROGENITOR CELLS; CELLULAR COMPOSITION; CEREBROSPINAL-FLUID; NEURONAL PRODUCTION; NESTIN EXPRESSION;
D O I
10.1186/1479-5876-12-75
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Prevailingly, adult mammalian neurogenesis is thought to occur in discrete, separate locations known as neurogenic niches that are best characterized in the subgranular zone (SGZ) of the dentate gyrus and in the subventricular zone (SVZ). The existence of adult human neurogenic niches is controversial. Methods: The existence of neurogenic niches was investigated with neurogenesis marker immunostaining in histologically normal human brains obtained from autopsies. Twenty-eight adult temporal lobes, specimens from limbic structures and the hypothalamus of one newborn and one adult were examined. Results: The neural stem cell marker nestin stained circumventricular organ cells and the immature neuronal marker doublecortin (DCX) stained hypothalamic and limbic structures adjacent to circumventricular organs; both markers stained a continuous structure running from the hypothalamus to the hippocampus. The cell proliferation marker Ki-67 was detected predominately in structures that form the septo-hypothalamic continuum. Nestin-expressing cells were located in the fimbria-fornix at the insertion of the choroid plexus; ependymal cells in this structure expressed the putative neural stem cell marker CD133. From the choroidal fissure in the temporal lobe, a nestin-positive cell layer spread throughout the SVZ and subpial zone. In the subpial zone, a branch of this layer reached the hippocampal sulcus and ended in the SGZ (principally in the newborn) and in the subiculum (principally in the adults). Another branch of the nestin-positive cell layer in the subpial zone returned to the optic chiasm. DCX staining was detected in the periventricular and middle hypothalamus and more densely from the mammillary body to the subiculum through the fimbria-fornix, thus running through the principal neuronal pathway from the hippocampus to the hypothalamus. The column of the fornix forms part of this pathway and appears to coincide with the zone previously identified as the human rostral migratory stream. Partial co-labeling with DCX and the neuronal marker beta III-tubulin was also observed. Conclusions: Collectively, these findings suggest the existence of an adult human neurogenic system that rises from the circumventricular organs and follows, at minimum, the circuitry of the hypothalamus and limbic system.
引用
收藏
页数:33
相关论文
共 50 条
  • [1] Existence of a potential neurogenic system in the adult human brain
    Adriano Barreto Nogueira
    Mari Cleide Sogayar
    Alison Colquhoun
    Sheila Aparecida Siqueira
    Ariel Barreto Nogueira
    Paulo Eurípedes Marchiori
    Manoel Jacobsen Teixeira
    Journal of Translational Medicine, 12
  • [2] Human adult neurogenic astrocytes: towards their recruitment for brain repair
    van Strien, M. E.
    Hol, E. M.
    JOURNAL OF NEUROCHEMISTRY, 2013, 125 : 32 - 32
  • [3] Androgens increase excitatory neurogenic potential in human brain organoids
    Iva Kelava
    Ilaria Chiaradia
    Laura Pellegrini
    Alex T. Kalinka
    Madeline A. Lancaster
    Nature, 2022, 602 : 112 - 116
  • [4] Androgens increase excitatory neurogenic potential in human brain organoids
    Kelava, Iva
    Chiaradia, Ilaria
    Pellegrini, Laura
    Kalinka, Alex T.
    Lancaster, Madeline A.
    NATURE, 2022, 602 (7895) : 112 - +
  • [5] IMMUNOLOGICAL REGULATION OF NEUROGENIC NICHES IN THE ADULT BRAIN
    Gonzalez-Perez, O.
    Gutierrez-Fernandez, F.
    Lopez-Virgen, V.
    Collas-Aguilar, J.
    Quinones-Hinojosa, A.
    Garcia-Verdugo, J. M.
    NEUROSCIENCE, 2012, 226 : 270 - 281
  • [6] Isolation and potential existence of side population cells in adult human kidney
    Inowa, Toshihiko
    Hishikawa, Keiichi
    Takeuchi, Takumi
    Kitamura, Tadaichi
    Fujita, Toshiro
    INTERNATIONAL JOURNAL OF UROLOGY, 2008, 15 (03) : 272 - 274
  • [7] A novel feature of the ancient organ: A possible involvement of the subcommissural organ in neurogenic/gliogenic potential in the adult brain
    Inada, Hitoshi
    Corales, Laarni Grace
    Osumi, Noriko
    FRONTIERS IN NEUROSCIENCE, 2023, 17
  • [8] Valproic acid exposure decreases neurogenic potential of outer radial glia in human brain organoids
    Zang, Zhenle
    Yin, Huachun
    Du, Zhulin
    Xie, Ruxin
    Yang, Ling
    Cai, Yun
    Wang, Liuyongwei
    Zhang, Dandan
    Li, Xin
    Liu, Tianyao
    Gong, Hong
    Gao, Junwei
    Yang, Hui
    Warner, Margaret
    Gustafsson, Jan-Ake
    Xu, Haiwei
    Fan, Xiaotang
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2022, 15
  • [9] Recalibrating the Existence of New Neurons in Adult Brain
    Dey, Jhilik
    Alam, Md Tanjim
    Chandra, Sreyashi
    Gandhi, Sonu
    Tripathi, Prem Prakash
    ACS CHEMICAL NEUROSCIENCE, 2019, 10 (05): : 2091 - 2093
  • [10] Histochemical analysis of two neurogenic regions in the adult ferret brain
    Takamori, Yasuharu
    Wakabayashi, Taketoshi
    Mori, Tetsuji
    Kitaya, Kotaro
    Kosaka, Jun
    Yamada, Hisao
    NEUROSCIENCE RESEARCH, 2009, 65 : S102 - S102