School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, Korea.
College of Life Science & Bioengineering, Korea Advanced Institute of Science & Technology (KAIST), Daejeon, Korea.
EMBO Rep. 2018 Nov;19(11). doi: 10.15252/embr.201846250. Epub 2018 Sep 17.
Coordinated expression of guidance molecules and their signal transduction are critical for correct brain wiring. Previous studies have shown that phospholipase C gamma1 (PLCγ1), a signal transducer of receptor tyrosine kinases, plays a specific role in the regulation of neuronal cell morphology and motility However, several questions remain regarding the extracellular stimulus that triggers PLCγ1 signaling and the exact role PLCγ1 plays in nervous system development. Here, we demonstrate that PLCγ1 mediates axonal guidance through a netrin-1/deleted in colorectal cancer (DCC) complex. Netrin-1/DCC activates PLCγ1 through Src kinase to induce actin cytoskeleton rearrangement. Neuronal progenitor-specific knockout of in mice causes axon guidance defects in the dorsal part of the mesencephalon during embryogenesis. Adult -deficient mice exhibit structural alterations in the corpus callosum, substantia innominata, and olfactory tubercle. These results suggest that PLCγ1 plays an important role in the correct development of white matter structure by mediating netrin-1/DCC signaling.
指导分子的协调表达及其信号转导对于大脑布线的正确形成至关重要。先前的研究表明,磷脂酶 C 伽马 1(PLCγ1)是受体酪氨酸激酶的信号转导物,在调节神经元细胞形态和运动方面发挥着特定的作用。然而,关于触发 PLCγ1 信号的细胞外刺激以及 PLCγ1 在神经系统发育中的确切作用,仍有几个问题需要解决。在这里,我们证明 PLCγ1 通过神经导向因子-1/结直肠癌缺失蛋白(DCC)复合物来介导轴突导向。神经导向因子-1/DCC 通过Src 激酶激活 PLCγ1,从而诱导肌动蛋白细胞骨架重排。在小鼠中神经元前体细胞特异性敲除 PLCγ1 会导致胚胎发育过程中中脑背侧的轴突导向缺陷。成年 PLCγ1 缺陷小鼠的胼胝体、无名质和嗅结节表现出结构改变。这些结果表明,PLCγ1 通过介导神经导向因子-1/DCC 信号在正确发育白质结构中发挥重要作用。