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Semaphorin 5A inhibits synaptogenesis in early postnatal- and adult-born hippocampal dentate granule cells.

Yuntao Duan | Shih-Hsiu Wang | Juan Song | Yevgeniya Mironova | Guo-li Ming | Alex L Kolodkin | Roman J Giger
eLife | 2014

Human SEMAPHORIN 5A (SEMA5A) is an autism susceptibility gene; however, its function in brain development is unknown. In this study, we show that mouse Sema5A negatively regulates synaptogenesis in early, developmentally born, hippocampal dentate granule cells (GCs). Sema5A is strongly expressed by GCs and regulates dendritic spine density in a cell-autonomous manner. In the adult mouse brain, newly born Sema5A-/- GCs show an increase in dendritic spine density and increased AMPA-type synaptic responses. Sema5A signals through PlexinA2 co-expressed by GCs, and the PlexinA2-RasGAP activity is necessary to suppress spinogenesis. Like Sema5A-/- mutants, PlexinA2-/- mice show an increase in GC glutamatergic synapses, and we show that Sema5A and PlexinA2 genetically interact with respect to GC spine phenotypes. Sema5A-/- mice display deficits in social interaction, a hallmark of autism-spectrum-disorders. These experiments identify novel intra-dendritic Sema5A/PlexinA2 interactions that inhibit excitatory synapse formation in developmentally born and adult-born GCs, and they provide support for SEMA5A contributions to autism-spectrum-disorders.

Pubmed ID: 25313870

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R01 HD069184
  • Agency: Howard Hughes Medical Institute, United States
  • Agency: NINDS NIH HHS, United States
    Id: NS048271
  • Agency: NIMH NIH HHS, United States
    Id: MH59199
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH059199
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS048271
  • Agency: NICHD NIH HHS, United States
    Id: HD069184
  • Agency: NINDS NIH HHS, United States
    Id: NS081281
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH105128
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS081281
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007315

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