Tao Yanmei, Dai Penggao, Liu Yu, Marchetto Sylvie, Xiong Wen-Cheng, Borg Jean-Paul, Mei Lin
Department of Neurology, Institute of Molecular Medicine and Genetics, Medical College of Georgia, Augusta, GA 30912, USA.
Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9477-82. doi: 10.1073/pnas.0901844106. Epub 2009 May 20.
Neuregulin 1 (NRG1) plays a critical role in myelination. However, little is known about regulatory mechanisms of NRG1 signaling. We show here that Erbin, a protein that contains leucine-rich repeats (LRR) and a PSD95-Dlg-Zol (PDZ) domain and that interacts specifically with ErbB2, is necessary for NRG1 signaling and myelination of peripheral nervous system (PNS). In Erbin null mice, myelinated axons were hypomyelinated with reduced expression of P0, a marker of mature myelinating Schwann cells (SCs), whereas unmyelinated axons were aberrantly ensheathed in Remak bundles, with increased numbers of axons in the bundles and in pockets. The morphological deficits were associated with decreased nerve conduction velocity and increased sensory threshold to mechanistic stimulation. These phenotypes were duplicated in erbin(DeltaC/DeltaC) mice, in which Erbin lost the PDZ domain to interact with ErbB2. Moreover, ErbB2 was reduced at protein levels in both Erbin mutant sciatic nerves, and ErbB2 became unstable and NRG1 signaling compromised when Erbin expression was suppressed. These observations indicate a critical role of Erbin in myelination and identify a regulatory mechanism of NRG1 signaling. Our results suggest that Erbin, via the PDZ domain, binds to and stabilizes ErbB2, which is necessary for NRG1 signaling that has been implicated in tumorigenesis, heart development, and neural function.
神经调节蛋白1(NRG1)在髓鞘形成中起关键作用。然而,关于NRG1信号传导的调节机制知之甚少。我们在此表明,Erbin是一种含有富含亮氨酸重复序列(LRR)和PSD95-Dlg-Zol(PDZ)结构域且能与ErbB2特异性相互作用的蛋白质,它对于NRG1信号传导和外周神经系统(PNS)的髓鞘形成是必需的。在Erbin基因敲除小鼠中,有髓轴突髓鞘形成减少,成熟髓鞘形成雪旺细胞(SCs)的标志物P0表达降低,而无髓轴突在Remak束中被异常包裹,束内和小凹中的轴突数量增加。这些形态学缺陷与神经传导速度降低和对机械刺激的感觉阈值升高有关。这些表型在erbin(DeltaC/DeltaC)小鼠中也有出现,在该小鼠中Erbin失去了与ErbB2相互作用的PDZ结构域。此外,在两种Erbin突变的坐骨神经中,ErbB2的蛋白水平均降低,当Erbin表达被抑制时,ErbB2变得不稳定,NRG1信号传导受损。这些观察结果表明Erbin在髓鞘形成中起关键作用,并确定了NRG1信号传导的一种调节机制。我们的结果表明,Erbin通过PDZ结构域与ErbB2结合并使其稳定,这对于与肿瘤发生、心脏发育和神经功能有关的NRG1信号传导是必需的。