Neurons generated in senescence maintain capacity for functional integration

Diano F. Marrone, Victor Ramirez-Amaya, Carol A Barnes

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Adult-born neurons in the dentate gyrus (DG) can survive for long periods, are capable of integrating into neuronal networks, and are important for hippocampus-dependent learning. Neurogenesis is dramatically reduced during senescence, and it remains unknown whether those few neurons that are produced remain capable of network integration. The expression of Arc, a protein coupled to neuronal activity, was used to measure activity among granule cells that were labeled with BrdU 4 months earlier in young (9 months) and aged (25 months) Fischer344 rats. The results indicate that while fewer cells are generated in the senescent DG, those that survive are (a) more likely to respond to spatial processing by expressing Arc relative to the remainder of the granule cell population and (b) equally responsive to spatial exploration as granule cells of the same age from young animals. These findings provide compelling evidence that newborn granule cells in the aged DG retain the capacity for participation in functional hippocampal networks.

Original languageEnglish (US)
Pages (from-to)1134-1142
Number of pages9
JournalHippocampus
Volume22
Issue number5
DOIs
StatePublished - May 2012

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Dentate Gyrus
Neurons
Neurogenesis
Bromodeoxyuridine
Hippocampus
Learning
Population
Proteins

Keywords

  • Aging
  • Arc
  • Dentate gyrus
  • Neurogenesis

ASJC Scopus subject areas

  • Cognitive Neuroscience

Cite this

Neurons generated in senescence maintain capacity for functional integration. / Marrone, Diano F.; Ramirez-Amaya, Victor; Barnes, Carol A.

In: Hippocampus, Vol. 22, No. 5, 05.2012, p. 1134-1142.

Research output: Contribution to journalArticle

Marrone, Diano F. ; Ramirez-Amaya, Victor ; Barnes, Carol A. / Neurons generated in senescence maintain capacity for functional integration. In: Hippocampus. 2012 ; Vol. 22, No. 5. pp. 1134-1142.
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