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Adult-born neurons modify excitatory synaptic transmission to existing neurons.
Adlaf, Elena W; Vaden, Ryan J; Niver, Anastasia J; Manuel, Allison F; Onyilo, Vincent C; Araujo, Matheus T; Dieni, Cristina V; Vo, Hai T; King, Gwendalyn D; Wadiche, Jacques I; Overstreet-Wadiche, Linda.
Affiliation
  • Adlaf EW; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Vaden RJ; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Niver AJ; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Manuel AF; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Onyilo VC; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Araujo MT; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Dieni CV; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Vo HT; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • King GD; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Wadiche JI; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
  • Overstreet-Wadiche L; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United States.
Elife ; 62017 01 30.
Article in En | MEDLINE | ID: mdl-28135190
Neurogenesis, the creation of new brain cells called neurons, occurs primarily before birth. However, a region of the brain called the dentate gyrus, which is involved in memory, continues to produce new neurons throughout life. Recent studies suggest that adding neurons to the dentate gyrus helps the brain to distinguish between similar sights, sounds and smells. This in turn makes it easier to encode similar experiences as distinct memories. The brain's outer layer, called the cortex, processes information from our senses and sends it, along with information about our location in space, to the dentate gyrus. By combining this sensory and spatial information, the dentate gyrus is able to generate a unique memory of an experience. But how does neurogenesis affect this process? As the dentate gyrus accumulates more neurons, the number of neurons in the cortex remains unchanged. Do some cortical neurons transfer their connections ­ called synapses ­ to the new neurons? Or does the brain generate additional synapses to accommodate the newborn cells? Adlaf et al. set out to answer this question by genetically modifying mice to alter the number of new neurons that could form in the dentate gyrus. Increasing the number of newborn neurons reduced the number of synapses between the cortex and the mature neurons in the dentate gyrus. Conversely, killing off newborn neurons had the opposite effect, increasing the strength of the synaptic connections to older cells. This suggests that new synapses are not formed to accommodate new neurons, but rather that there is a redistribution of synapses between old and new neurons in the dentate gyrus. Further work is required to determine how this redistribution of synapses contributes to how the dentate gyrus works. Does redistributing synapses disrupt existing memories? And how do these findings relate to the effects of exercise ­ does this natural way of increasing neurogenesis increase the overall number of synapses in the system, potentially creating enough connections for both new and old neurons?
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Synaptic Transmission / Dentate Gyrus / Excitatory Postsynaptic Potentials / Neurogenesis / Nerve Net / Neurons Limits: Animals Language: En Journal: Elife Year: 2017 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Synaptic Transmission / Dentate Gyrus / Excitatory Postsynaptic Potentials / Neurogenesis / Nerve Net / Neurons Limits: Animals Language: En Journal: Elife Year: 2017 Type: Article Affiliation country: United States