Matsumoto Hideko, Nagashima Masabumi
Department of Anatomy, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama-machi, Iruma-gun, Saitama, 350-0495, Japan.
BMC Neurosci. 2017 Oct 17;18(1):74. doi: 10.1186/s12868-017-0392-x.
Netrin-1, a multifunctional axon guidance cue, elicits axon outgrowth via one of its receptors deleted in colorectal cancer (DCC) in several types of neurons, including cerebral cortical neurons of embryonic mice. However, we and others have observed de novo formation of axon branches without axon outgrowth induced by netrin-1 in cortical culture of neonatal hamsters. These previous reports suggested the possibility that netrin-1 function might alter during development, which we here investigated using dissociated culture prepared from cerebral cortices of embryonic mice.
Imaging analysis revealed netrin-1-induced outgrowth in embryonic day (E) 14 axons and netrin-1-induced branching in E16 axons. Netrin-1-evoked filopodial protrusions, which sprouted on the shafts of E16 axons preceding branch formation, were visualized by a novel method called atmospheric scanning electron microscopy. Treatment with an anti-DCC function-blocking antibody affected both axon outgrowth and branching.
Morphological analyses suggested a possibility of a shift in the function of netrin-1 in cortical axons during development, from promotion of outgrowth to promotion of branch formation starting with filopodial protrusion. Function-blocking experiments suggested that DCC may contribute not only to axon outgrowth but branching.
Netrin-1是一种多功能轴突导向因子,可通过其在几种类型的神经元(包括胚胎小鼠的大脑皮质神经元)中一种名为结直肠癌缺失基因(DCC)的受体来引发轴突生长。然而,我们和其他人在新生仓鼠的皮质培养物中观察到,Netrin-1可诱导轴突分支的从头形成,而不会引起轴突生长。这些先前的报告表明,Netrin-1的功能可能在发育过程中发生改变,我们在此使用从胚胎小鼠大脑皮质制备的解离培养物对此进行了研究。
成像分析显示,Netrin-1可诱导胚胎第14天(E14)轴突生长,以及E16轴突分支。通过一种名为常压扫描电子显微镜的新方法,可以观察到在E16轴突形成分支之前,Netrin-1诱发的丝状伪足在轴突干上发芽。用抗DCC功能阻断抗体处理会影响轴突生长和分支。
形态学分析表明,在发育过程中,Netrin-1在皮质轴突中的功能可能发生转变,从促进生长转变为从丝状伪足突起开始促进分支形成。功能阻断实验表明,DCC不仅可能有助于轴突生长,还可能有助于分支形成。