Rhiner Christa, Gysi Stephan, Fröhli Erika, Hengartner Michael O, Hajnal Alex
Institute of Molecular Biology, University of Zurich, 8057, Switzerland.
Development. 2005 Oct;132(20):4621-33. doi: 10.1242/dev.02042. Epub 2005 Sep 21.
During nervous system development, axons that grow out simultaneously in the same extracellular environment are often sorted to different target destinations. As there is only a restricted set of guidance cues known, regulatory mechanisms are likely to play a crucial role in controlling cell migration and axonal pathfinding. Heparan sulfate proteoglycans (HSPGs) carry long chains of differentially modified sugar residues that have been proposed to encode specific information for nervous system development. Here, we show that the cell surface proteoglycan syndecan SDN-1 functions autonomously in neurons to control the neural migration and guidance choices of outgrowing axons. Epistasis analysis suggests that heparan sulfate (HS) attached to SDN-1 can regulate guidance signaling by the Slit/Robo pathway. Furthermore, SDN-1 acts in parallel with other HSPG core proteins whose HS side chains are modified by the C5-epimerase HSE-5, and/or the 2O-sulfotransferase HST-2, depending on the cellular context. Taken together, our experiments show that distinct HS modification patterns on SDN-1 are involved in regulating axon guidance and cell migration in C. elegans.
在神经系统发育过程中,在相同细胞外环境中同时长出的轴突通常会被导向不同的目标位置。由于已知的导向线索种类有限,调控机制可能在控制细胞迁移和轴突寻路中起关键作用。硫酸乙酰肝素蛋白聚糖(HSPG)带有长链的差异修饰糖残基,有人提出这些糖残基可为神经系统发育编码特定信息。在此,我们表明细胞表面蛋白聚糖syndecan SDN-1在神经元中自主发挥作用,以控制轴突生长过程中的神经迁移和导向选择。上位性分析表明,与SDN-1相连的硫酸乙酰肝素(HS)可通过Slit/Robo途径调节导向信号。此外,根据细胞环境,SDN-1与其他HSPG核心蛋白并行发挥作用,这些核心蛋白的HS侧链由C5-表异构酶HSE-5和/或2-O-磺基转移酶HST-2修饰。综上所述,我们的实验表明,SDN-1上不同的HS修饰模式参与调控秀丽隐杆线虫的轴突导向和细胞迁移。