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

机译:通过NRG1 / erbB4介导的kalirin-7抑制作用控制神经元间树突的生长。

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摘要

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.
机译:神经调节蛋白1(NRG1)是一种分泌的营养因子,可激活突触后的erbB4受体酪氨酸激酶。 NRG1和erbB4均已反复与精神分裂症相关,但其下游靶标尚不明确。 ErbB4在中间神经元中高度丰富,并且已显示NRG1介导的erbB4激活可调节中间神经元功能,但人们对NRG1-erbB4信号在调节中间神经元树突生长中的作用尚不甚了解。在这里,我们显示NRG1 / erbB4通过主要的树突状Rac1-GEF卡里林促进成熟中间神经元中树突的生长。最近的研究表明,KALRN基因与精神分裂症有关。我们的数据表明,在卡利林7的C末端,磷酸化是这些作用的关键部位。随着精神分裂症中神经元树突长度的减少,了解NRG1-erbB4信号如何调节神经元树突形态发生可能会揭示与疾病相关的皮质回路改变。

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