Pischedda Francesca, Piccoli Giovanni
Department of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano Milano, Italy.
Department of Neuroscience, Istituto Di Neuroscienze-Consiglio Nazionale delle Ricerche, San Raffaele Scientific Park Milano, Italy.
Front Mol Neurosci. 2016 Jan 13;8:89. doi: 10.3389/fnmol.2015.00089. eCollection 2015.
IgLON proteins are GPI anchored adhesion molecules that control neurite outgrowth. In particular, Negr1 down-regulation negatively influences neuronal arborization in vitro and in vivo. In the present study, we found that the metalloprotease ADAM10 releases Negr1 from neuronal membrane. Ectodomain shedding influences several neuronal mechanisms, including survival, synaptogenesis, and the formation of neurite trees. By combining morphological analysis and virus-mediated selective protein silencing in primary murine cortical neurons, we found that pharmacologically inhibition of ADAM10 results in an impairment of neurite tree maturation that can be rescued upon treatment with soluble Negr1. Furthermore, we report that released Negr1 influences neurite outgrowth in a P-ERK1/2 and FGFR2 dependent manner. Together our findings suggest a role for Negr1 in regulating neurite outgrowth through the modulation of FGFR2 signaling pathway. Given the physiological and pathological role of ADAM10, Negr1, and FGFR2, the regulation of Negr1 shedding may play a crucial role in sustaining brain function and development.
IgLON蛋白是糖基磷脂酰肌醇(GPI)锚定的粘附分子,可控制神经突生长。特别是,Negr1的下调会对体外和体内的神经元分支产生负面影响。在本研究中,我们发现金属蛋白酶ADAM10可从神经元膜上释放Negr1。胞外域脱落影响多种神经元机制,包括存活、突触形成和神经突树的形成。通过在原代小鼠皮层神经元中结合形态学分析和病毒介导的选择性蛋白沉默,我们发现对ADAM10的药理学抑制会导致神经突树成熟受损,而用可溶性Negr1处理后可得到挽救。此外,我们报告释放的Negr1以依赖P-ERK1/2和FGFR2的方式影响神经突生长。我们的研究结果共同表明Negr1在通过调节FGFR2信号通路来调节神经突生长中发挥作用。鉴于ADAM10、Negr1和FGFR2的生理和病理作用,Negr1脱落调控可能在维持脑功能和发育中起关键作用。