Interneuronal DISC1 regulates NRG1-ErbB4 signalling and excitatory-inhibitory synapse formation in the mature cortex.

نویسندگان

  • Saurav Seshadri
  • Travis Faust
  • Koko Ishizuka
  • Kristen Delevich
  • Youjin Chung
  • Sun-Hong Kim
  • Martis Cowles
  • Minae Niwa
  • Hanna Jaaro-Peled
  • Toshifumi Tomoda
  • Cary Lai
  • E S Anton
  • Bo Li
  • Akira Sawa
چکیده

Neuregulin-1 (NRG1) and its receptor ErbB4 influence several processes of neurodevelopment, but the mechanisms regulating this signalling in the mature brain are not well known. DISC1 is a multifunctional scaffold protein that mediates many cellular processes. Here we present a functional relationship between DISC1 and NRG1-ErbB4 signalling in mature cortical interneurons. By cell type-specific gene modulation in vitro and in vivo including in a mutant DISC1 mouse model, we demonstrate that DISC1 inhibits NRG1-induced ErbB4 activation and signalling. This effect is likely mediated by competitive inhibition of binding of ErbB4 to PSD95. Finally, we show that interneuronal DISC1 affects NRG1-ErbB4-mediated phenotypes in the fast spiking interneuron-pyramidal neuron circuit. Post-mortem brain analyses and some genetic studies have reported interneuronal deficits and involvement of the DISC1, NRG1 and ErbB4 genes in schizophrenia, respectively. Our results suggest a mechanism by which cross-talk between DISC1 and NRG1-ErbB4 signalling may contribute to these deficits.

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عنوان ژورنال:
  • Nature communications

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2015