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Optical controlling reveals time-dependent roles for adult-born dentate granule cells

Optical controlling reveals time-dependent roles for adult-born dentate granule cells. Yan Gu, Maithe Arruda-Carvalho, Jia Wang, Stephen R Janoschka , Sheena A Josselyn , Paul W Frankland & Shaoyu Ge. Background. The adult hippocampus continues to give rise to several

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Optical controlling reveals time-dependent roles for adult-born dentate granule cells

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  1. Optical controlling reveals time-dependent roles for adult-born dentate granule cells Yan Gu, Maithe Arruda-Carvalho, Jia Wang, Stephen R Janoschka, Sheena A Josselyn, Paul W Frankland & Shaoyu Ge

  2. Background The adult hippocampus continues to give rise to several thousand new dentate granule cells everyday. Studies using global perturbation or ablation of adult hippocampal neurogenesis has revealed deficits in some forms of hippocampal memory. .

  3. Background As the morphological and physiological phenotypes of adult-born cells change markedly as they mature, they may have distinct roles at different stages following integration into hippocampal circuits. Adult-born dentate granule cells (DGCs) extend dendritesreceive functional input from the existing neural circuits as early as 2 weeks after birth. Input (dendritic) synapses of adult-born neurons show enhanced plasticity between 4–6 weeks after birth compared with other stages.

  4. Questions What is the precise timing for these adult-born functional output synapse formation andmaturation? Whether do output synapses, if formed and functional, also exhibit heightened plasticity around the same time? What is its functional role?

  5. Retroviral birth-dating + Gene delivery (EGFP+ Light gated ion channels) Optogenetic stimulation Electrophysiological experiments Behavioral experiments Synaptic transmission efficiency, Capability of LTP Water maze Classical fear conditioning Methods

  6. Results Birth-dating and labeling newborn DGCs Labeling specificity of newborn DGCs with high-titer retrovirus No mature DGC-like cells at 1 and 2 wpi Experimental timeline

  7. Results Adult-born neurons form functional synapses on CA3 pyramidal neurons Adult-born DGCs fully integrate into the hippocampal trisynaptic circuits by ~4 wpi

  8. Results Heightened synaptic plasticity of young adult-born neurons

  9. Results Output synapses of mature newborn DGCs remain plastic, but have a higher induction threshold Young newborn neurons exhibit heightened plasticity that peaks at ~4 wpi

  10. Conclusion 1 • Adult-born DGCs fully incorporate into the hippocampal trisynaptic neural circuit around 4 wpi and DGCs at this age have more excitable membranes and enhanced input/output synaptic plasticity.

  11. Results Optical silencing of newborn DGCs does not influence acquisition of spatialmemory

  12. Results Silencing young newborn neurons affects spatialmemory retrieval labeled ~4-week-old adult-born DGCs regulate spatial memory retrieval.

  13. Results Silencing young newborn neurons impairs retrival of contextural fear memory

  14. Results The behavioral role for newborn DGCs relies on their age

  15. Results Heightened plasticity in young newborn neurons may be important for memory retrieval

  16. Results Silencing newborn neurons at 4 wpi, but not 8 wpi, disrupted memory retrieval in both tasks

  17. Conclusion 2 • Adult-born neurons may be transiently critical for memory retrieval, but the effect, at least in spatial and contextual memory retrieval, may decline as these adult-born neurons continue to mature.

  18. Thank you

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