Barnett Mark W, Fisher Carolyn E, Perona-Wright Georgia, Davies Jamie A
Edinburgh University Medical School, Teviot Place, Edinburgh EH8 9AG, UK.
J Cell Sci. 2002 Dec 1;115(Pt 23):4495-503. doi: 10.1242/jcs.00114.
Glial cell line-derived neurotrophic factor, GDNF, is vital to the development and maintenance of neural tissues; it promotes survival of sympathetic, parasympathetic and spinal motor neurons during development, protects midbrain dopaminergic neurons from apoptosis well enough to be a promising treatment for Parkinson's disease, and controls renal and testicular development. Understanding how GDNF interacts with its target cells is therefore a priority in several fields. Here we show that GDNF requires glycosaminoglycans as well as the already-known components of its receptor complex, c-Ret and GFRalpha-1. Without glycosaminoglcyans, specifically heparan sulphate, c-Ret phosphorylation fails and GDNF cannot induce axonogenesis in neurons, in PC-12 cells, or scatter of epithelial cells. Furthermore, exogenous heparan sulphate inhibits rather than assists GDNF signalling. The involvement of heparan sulphates in GDNF signalling raises the possibility that modulation of heparan expression may modulate signalling by GDNF in vivo.
胶质细胞系源性神经营养因子(GDNF)对于神经组织的发育和维持至关重要;它在发育过程中促进交感神经、副交感神经和脊髓运动神经元的存活,足以保护中脑多巴胺能神经元免于凋亡,有望成为治疗帕金森病的方法,并且控制肾脏和睾丸的发育。因此,了解GDNF如何与其靶细胞相互作用是多个领域的首要任务。在这里,我们表明GDNF需要糖胺聚糖以及其受体复合物的已知组分c-Ret和GFRalpha-1。没有糖胺聚糖,特别是硫酸乙酰肝素,c-Ret磷酸化失败,并且GDNF不能在神经元、PC-12细胞中诱导轴突形成,也不能诱导上皮细胞分散。此外,外源性硫酸乙酰肝素抑制而非协助GDNF信号传导。硫酸乙酰肝素参与GDNF信号传导增加了在体内调节硫酸乙酰肝素表达可能调节GDNF信号传导的可能性。