Neurogenesis in the Dentate Gyrus of the Adult Tree Shrew Is Regulated by Psychosocial Stress and NMDA Receptor Activation

These studies were designed to determine whether adult neurogenesis occurs in the dentate gyrus of the tree shrew, an animal phylogenetically between insectivores and primates, and to explore the possibility that this process is regulated by stressful experiences and NMDA receptor activation. We performed immunohistochemistry for cell-specific markers and the thymidine analog bromodeoxyuridine (BrdU), a marker of DNA synthesis that labels proliferating cells and their progeny, on the brains of adult tree shrews subjected to psychosocial stress or NMDA receptor antagonist treatment. Cells that incorporated BrdU in the dentate gyrus of adult tree shrews were primarily located in the subgranular zone, had morphological characteristics of granule neuron precursors, and appeared to divide within 24 hr after BrdU injection. Three weeks after BrdU injection, BrdU-labeled cells had neuronal morphology, expressed the neuronal marker neuron specific enolase, and were incorporated into the granule cell layer. Vimentin-immunoreactive radial glia were observed in the dentate gyrus with cell bodies in the subgranular zone and processes extending into the granule cell layer. Exposure to acute psychosocial stress resulted in a rapid decrease in the number of BrdU-labeled cells in the dentate gyrus. In contrast, blockade of NMDA receptors, with the NMDA receptor antagonist MK-801, resulted in an increase in the number of BrdU-labeled cells in the dentate gyrus. These results indicate that adult neurogenesis occurs in the tree shrew dentate gyrus and is regulated by a stressful experience and NMDA receptor activation. Furthermore, we suggest that these characteristics may be common to most mammalian species.

[1]  B. Cragg,et al.  Some reflexes mediated by the afferent fibers of the abdominal vagus in the rabbit and cat. , 1960, Experimental neurology.

[2]  Angevine Jb Time of neuron origin in the hippocampal region. An autoradiographic study in the mouse. , 1965 .

[3]  J. B. Angevine Time of neuron origin in the hippocampal region. An autoradiographic study in the mouse. , 1965, Experimental neurology. Supplement.

[4]  J. Altman,et al.  Postnatal Neurogenesis in the Guinea-pig , 1967, Nature.

[5]  R. Skalko,et al.  Incorportaiton of thymidine and its analogue, bromodeoxyuridine, into embryos and maternal tissues of the mouse. , 1973, Differentiation; research in biological diversity.

[6]  W. Cowan,et al.  An autoradiographic study of the time of origin and the pattern of granule cell migration in the dentate gyrus of the rat , 1975, The Journal of comparative neurology.

[7]  J. Hinds,et al.  Neurogenesis in the adult rat: electron microscopic analysis of light radioautographs. , 1977, Science.

[8]  P. Rakić,et al.  The time of origin of neurons in the hippocampal region of the rhesus monkey , 1981, The Journal of comparative neurology.

[9]  A. Privat,et al.  Subgranular zone of the dentate gyrus of young rabbits as a secondary matrix. A high-resolution autoradiographic study. , 1982, Developmental neuroscience.

[10]  R. Sutherland,et al.  A behavioural analysis of spatial localization following electrolytic, kainate- or colchicine-induced damage to the hippocampal formation in the rat , 1983, Behavioural Brain Research.

[11]  D. H. Bell,et al.  Mitotic neuroblasts in the 9-day-old and 11-month-old rodent hippocampus , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  B. Sripanidkulchai,et al.  The development of Ammon's horn and the fascia dentata in the cat: a [3H]thymidine analysis. , 1985, Brain research.

[13]  I. Whishaw Hippocampal, granule cell and CA3–4 lesions impair formation of a place learning-set in the rat and induce reflex epilepsy , 1987, Behavioural Brain Research.

[14]  P. Rakić,et al.  Nature and fate of proliferative cells in the hippocampal dentate gyrus during the life span of the rhesus monkey , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  M. Miller,et al.  Bromodeoxyuridine immunohistochemical determination of the lengths of the cell cycle and the DNA-synthetic phase for an anatomically defined population , 1989, Journal of neurocytology.

[16]  J. Altman,et al.  Mosaic organization of the hippocampal neuroepithelium and the multiple germinal sources of dentate granule cells , 1990, The Journal of comparative neurology.

[17]  R. Martin Primate origins and evolution , 1990 .

[18]  J. Altman,et al.  Migration and distribution of two populations of hippocampal granule cell precursors during the perinatal and postnatal periods , 1990, The Journal of comparative neurology.

[19]  M. Schumacher,et al.  Psychosocial stress affects pineal function in the tree shrew (Tupaia belangeri) , 1990, Physiology & Behavior.

[20]  H. Cameron,et al.  Adrenal hormones suppress cell division in the adult rat dentate gyrus , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  Joseph E LeDoux,et al.  Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning. , 1992, Behavioral neuroscience.

[22]  J. Korf,et al.  A single social stress-experience alters glutamate receptor-binding in rat hippocampal CA3 area , 1993, Neuroscience Letters.

[23]  H. Cameron,et al.  Differentiation of newly born neurons and glia in the dentate gyrus of the adult rat , 1993, Neuroscience.

[24]  D. Pfaff,et al.  RB and Cdc2 expression in brain: correlations with 3H-thymidine incorporation and neurogenesis , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  B Kirschenbaum,et al.  In vitro neuronal production and differentiation by precursor cells derived from the adult human forebrain. , 1994, Cerebral cortex.

[26]  H. Cameron,et al.  Adult neurogenesis is regulated by adrenal steroids in the dentate gyrus , 1994, Neuroscience.

[27]  R. Sapolsky,et al.  Glucocortcoids mediate the stress-induced extracellular accumulation of glutamate , 1994, Brain Research.

[28]  C. H. Vanderwolf,et al.  Components of weasel and fox odors elicit fast wave bursts in the dentate gyrus of rats , 1994, Behavioural Brain Research.

[29]  岡野 James洋尚 RB and Cdc2 expression in brain : correlations with [3]H-thymidine incorporation and neurogenesis , 1994 .

[30]  D. Jezova,et al.  Stress-induced changes in messenger RNA levels of N-methyl-d-aspartate and AMPA receptor subunits in selected regions of the rat hippocampus and hypothalamus , 1995, Neuroscience.

[31]  H. Cameron,et al.  Regulation of adult neurogenesis by excitatory input and NMDA receptor activation in the dentate gyrus , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  B. McEwen,et al.  Chronic Psychosocial Stress Causes Apical Dendritic Atrophy of Hippocampal CA3 Pyramidal Neurons in Subordinate Tree Shrews , 1996, The Journal of Neuroscience.

[33]  T. Palmer,et al.  Neurogenesis in the dentate gyrus of the adult rat: age-related decrease of neuronal progenitor proliferation , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  Christoph Hiemke,et al.  Psychosocial stress in tree shrews: Clomipramine counteracts behavioral and endocrine changes , 1996, Pharmacology Biochemistry and Behavior.