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21 - Immature neurons in the adult brain. Breaking all the rules

Published online by Cambridge University Press:  05 December 2011

J. Martin Wojtowicz
Affiliation:
University of Toronto
Narinder Kapur
Affiliation:
University College London
Alvaro Pascual-Leone
Affiliation:
Harvard Medical School
Vilayanur Ramachandran
Affiliation:
University of California, San Diego
Jonathan Cole
Affiliation:
University of Bournemouth
Sergio Della Sala
Affiliation:
University of Edinburgh
Tom Manly
Affiliation:
MRC Cognition and Brain Sciences Unit
Andrew Mayes
Affiliation:
University of Manchester
Oliver Sacks
Affiliation:
Columbia University Medical Center
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Summary

Summary

Paradoxes in the field of adult neurogenesis are many. This may be partly due to the fact that this field of research is relatively new and that ideas outpace hard facts. Moreover, evidence originating from different laboratories is often inconsistent due to varied experimental conditions. We will not concern ourselves with such trivial controversies, but instead try to point out the perceived inconsistencies that may represent true exceptions to the rule. Such paradoxes make one pause and wonder about accepted theories, and importantly, may point us in new and creative directions.

The chapter begins with an explanation of neurogenesis in the context of brain anatomy. Description of neuronal ‘assembly line’ is followed by explanation of what new neurons look like and how they function. At the end of this chapter the reader will realize that the very existence of adult neurogenesis is still denied by some, and that most debates are yet to be settled.

Glossary

Apoptosis – a type of cell death resulting from a sequence of chemical reactions within the cell. It can be triggered ‘on purpose’ to eliminate excessive cell numbers during brain growth.

Contextual learning – a type of learning depending strongly on the context in which the learning took place. Often associated with specific brain structures such as the hippocampus.

Entorhinal cortex – part of the cortex immediately adjacent to the hippocampus. It contains neurons that send information to and receive information from the hippocampus.

Hippocampal formation – includes three main brain components constituting neuronal circuitry responsible for learning.

Type
Chapter
Information
The Paradoxical Brain , pp. 365 - 378
Publisher: Cambridge University Press
Print publication year: 2011

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References

Abrous, D. N., & Wojtowicz, J. M. (2008). Neurogenesis and the hippocampal memory system. In: Gage, F. H., Kempermann, G., & Song, H.-J. (Eds.). Adult Neurogenesis. New York, NY: Cold Spring Harbor Laboratory Press, pp. 445–62.Google Scholar
Altman, J., & Bayer, S. A. (1990). Mosaic organization of the hippocampal neuroepithelium and the multiple germinal sources of dentate granule cells. Journal of Comparative Neurology, 301: 325–42.CrossRefGoogle ScholarPubMed
Altman, J., & Das, G. D. (1965). Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats. Journal of Comparative Neurology, 124: 319–36.CrossRefGoogle ScholarPubMed
Amrein, I., Boonstra, R., Lipp, H.-P., & Wojtowicz, J. M. (2008). Adult hippocampal neurogenesis in natural populations of mammals. In: Gage, F. H., Kempermann, G., & Song, H.-J. (Eds.). Adult Neurogenesis. New York, NY: Cold Spring Harbor Laboratory Press, pp. 645–59.Google Scholar
Amrein, I., Dechmann, D. K., Winter, Y., & Lipp, H.-P. (2007). Absent or low rate of adult neurogenesis in the hippocampus of bats (chiroptera). PLoS ONE, 2: e455.CrossRefGoogle Scholar
Atwood, H. L., & Wojtowicz, J. M. (1999). Silent synapse in neural plasticity: current evidence. Learning & Memory, 6: 542–71.CrossRefGoogle ScholarPubMed
Ben-Ari, Y., Khazipov, R., Leinekugel, X., Caillard, O., & Gaiarasa, J.-L. (1997). GABAA, NMDA and AMPA receptors: a developmentally regulated ‘menage a trois’. Trends in Neuroscience, 20: 523–9.CrossRefGoogle Scholar
Cameron, H. A., & McKay, R. D. G. (2001). Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus. Journal of Comparative Neurology, 435: 406–17.CrossRefGoogle ScholarPubMed
Cohen, N. J., & Eichenbaum, H. (1993). Memory, Amnesia and the Hippocampal System, 1st ed. Cambridge, MA: The MIT Press.Google Scholar
Castro, F. (2009). Wiring olfaction: the cellular and molecular mechanisms that guide the development of synaptic connections from the nose to the cortex. Frontiers in Neurogenesis, 1: 4. doi:10.3389/neuro.Google Scholar
Dupret, D., Fabre, A., Dobrossy, M. D., et al. (2007). Spatial learning depends on both the addition and removal of new hippocampal neurons. PLoS biology, 5: 1683–94.CrossRefGoogle ScholarPubMed
Epp, J. R., Barker, J. M., & Galea, L. A. M. (2009). Running wild: neurogenesis in the hippocampus across the lifespan in wild and laboratory-bred norway rats. Hippocampus, 19: 1040–9.CrossRefGoogle ScholarPubMed
Ge, S., Pradhan, D. A., Ming, G.-I., & Song, H. (2007). GABA sets the tempo for activity-dependent adult neurogenesis. Trends in Neuroscience, 30: 1–8.CrossRefGoogle ScholarPubMed
Gould, E., Beylin, A., Tanapat, P., Reeves, A. J., & Shors, T. J. (1999). Learning enhances adult neurogenesis in the hippocampal formation. Nature Neuroscience, 2: 260–5.CrossRefGoogle ScholarPubMed
Gross, C. G. (2000). Neurogenesis in the adult brain: death of a dogma. Nature Reviews, 1: 67–73.CrossRefGoogle ScholarPubMed
Kempermann, G. (2008). The neurogenic reserve hypothesis: what is adult hippocampal neurogenesis good for?Trends in Neuroscience, 31: 163–214.CrossRefGoogle Scholar
Kuhn, H. G. (2008). The balance of trophic support and cell death in adult neurogenesis. In: Gage, F. H., Kempermann, G., & Song, H.-J. (Eds.). Adult Neurogenesis. New York, NY: Cold Spring Harbor Laboratory Press.Google Scholar
McDonald, H. Y., & Wojtowicz, J. M. (2005). Dynamics of neurogenesis in the dentate gyrus of adult rats. Neuroscience Letters, 385: 70–5.CrossRefGoogle ScholarPubMed
Nithianantharajah, J., & Hannan, A. J. (2006). Enriched environments, experience-dependent plasticity and disorders of the nervous system. National Review of Neuroscience, 7: 697–709.CrossRefGoogle ScholarPubMed
Rakic, P. (1985). Limits of neurogenesis in primates. Science, 227: 1054–8.CrossRefGoogle ScholarPubMed
Shors, T. J. (2009). Saving new brain cells. Scientific American, 3: 47–54.Google Scholar
Snyder, J. S., Choe, J.,Clifford, M., et al. (2009). Adult-born hippocampal neurons are more numerous, faster maturing and more involved in behavior in rats than in mice. Journal of Neuroscience, 29: 14,484–95.CrossRefGoogle ScholarPubMed
Snyder, J. S., Hong, N., McDonald, R. J., & Wojtowicz, J. M. (2005). A role for adult hippocampal neurogenesis in spatial long-term memory. Neuroscience, 130: 843–52.CrossRefGoogle ScholarPubMed
Snyder, J. S., Kee, N., & Wojtowicz, J. M. (2001). Effects of adult neurogenesis on synaptic plasticity in the rat dentate gyrus. Journal of Neurophysiology, 85: 2423–31.CrossRefGoogle ScholarPubMed
Snyder, J. S., Radik, R., Wojtowicz, J. M., & Cameron, H. A. (2008). Anatomical gradients of neurogenesis and activity: young neurons in the ventral dentate gyrus are activated by water maze training. Hippocampus, 19: 360–70.CrossRefGoogle Scholar
Squire, L. R. (1992). Memory and the hippocampus: a synthesis from findings with rats, monkeys and humans. Psychology Review, 99: 195–231.CrossRefGoogle ScholarPubMed
Sun, W., Winseck, A., Vinsant, S., Park, O., Kim, H., & Oppenheim, R. W. (2004). Programmed cell death of adult-generated hippocampal neurons is mediated by the preapoptotic gene Bax. Journal of Neuroscience, 24: 11,205–13.CrossRefGoogle Scholar
Valenzuela, M. J., & Sachdev, P. (2006). Brain reserve and dementia: a systematic review. Psychological Medicine, 36: 441–54.CrossRefGoogle ScholarPubMed
Praag, H., Schinder, A. F., Christie, B. R., Toni, N., Palmer, T. D., & Gage, F. H. (2002). Functional neurogenesis in the adult hippocampus. Nature, 415: 1030–4.CrossRefGoogle ScholarPubMed
Wang, J.-W., David, D. J., Monckton, J. E., Battaglia, F., & Hen, R. (2008). Chronic fluoxetine stimulates maturation and synaptic plasticity of adult born hippocampal granule cells. Journal of Neuroscience, 28: 1374–84.CrossRefGoogle ScholarPubMed
Wang, S., Scott, B. W., & Wojtowicz, J. M. (2000). Heterogenous properties of dentate gyrus granule neurons in the adult rat. Journal of Neurobiology, 42: 248–57.3.0.CO;2-J>CrossRefGoogle ScholarPubMed
Wilbrecht, L., Crionas, A., & Nottebohm, F. (2002). Experience affects recrutiment of new neurons but not adult neuron number. Journal of Neuroscience, 22: 825–31.CrossRefGoogle Scholar
Winocur, G., Wojtowicz, J. M., Sekers, M., Snyder, J. S., & Wang, S. (2006). Inhibition of neurogenesis interferes with hippocampal-dependent memory function. Hippocampus, 16: 296–304.CrossRefGoogle Scholar
Wojtowicz, J. M. (2008). Potential consequences of altered neurogenesis on learning and memory in the epileptic brain. Epilepsia, 49(Suppl. 5): 42–9.CrossRefGoogle ScholarPubMed

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