4.8 Article

Control of interneuron dendritic growth through NRG1/erbB4-mediated kalirin-7 disinhibition

Journal

MOLECULAR PSYCHIATRY
Volume 17, Issue 1, Pages 99-107

Publisher

SPRINGERNATURE
DOI: 10.1038/mp.2011.35

Keywords

PSD-95; fyn; src

Funding

  1. NIH-NIMH [R01MH071316]
  2. National Alliance for Research on Schizophrenia and Depression (NARSAD)
  3. NIH [MH078833]
  4. Ruth L Kirschstein National Research Service [1F31AG031621-01A2, 1F31MH085362]
  5. Christopher Reeve Foundation

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Neuregulin 1 (NRG1) is a secreted trophic factor that activates the postsynaptic erbB4 receptor tyrosine kinase. Both NRG1 and erbB4 have been repeatedly associated with schizophrenia, but their downstream targets are not well characterized. ErbB4 is highly abundant in interneurons, and NRG1-mediated erbB4 activation has been shown to modulate interneuron function, but the role for NRG1-erbB4 signaling in regulating interneuron dendritic growth is not well understood. Here we show that NRG1/erbB4 promote the growth of dendrites in mature interneurons through kalirin, a major dendritic Rac1-GEF. Recent studies have shown associations of the KALRN gene with schizophrenia. Our data point to an essential role of phosphorylation in kalirin-7's C terminus as the critical site for these effects. As reduced interneuron dendrite length occurs in schizophrenia, understanding how NRG1-erbB4 signaling modulates interneuron dendritic morphogenesis might shed light on disease-related alterations in cortical circuits. Molecular Psychiatry (2012) 17, 99-107; doi:10.1038/mp.2011.35; published online 12 April 2011

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