Campenot R B, Soin J, Blacker M, Lund K, Eng H, MacInnis B L
Department of Cell Biology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada T6G 2H7.
Neuropharmacology. 2003 Jun;44(8):1107-17. doi: 10.1016/s0028-3908(03)00042-x.
Disruption of the Golgi by brefeldin A (BFA) has been reported to block fast axonal transport and axonal growth. We used compartmented cultures of rat sympathetic neurons to investigate its effects on slow axonal transport. BFA (1 micro g/ml) applied to cell bodies/proximal axons for 6-20 h disrupted the Golgi, reversibly blocked axonal growth, and reversibly blocked anterograde transport of all proteins, including tubulin. The retrograde transport of nerve growth factor (NGF) was also blocked. The phosphorylation of Erk1 and Erk2 in response to NGF was unaffected after 6 h of treatment with BFA, suggesting that the block of axonal transport was specific and direct. Consistent with its principal site of action at the Golgi, no effects were observed when BFA was applied only to the distal axons. Block of fast anterograde and retrograde axonal transport is consistent with the role of the Golgi in supplying transport vesicles. Block of slow axonal transport was surprising, and further results indicated that transport of tubulin en route along the axon was arrested by application of BFA to the cell bodies, suggesting that a continuous supply of anterograde transport vesicles from the Golgi is required to maintain slow axonal transport of cytoskeletal proteins.
据报道,布雷菲德菌素A(BFA)破坏高尔基体可阻断快速轴突运输和轴突生长。我们使用大鼠交感神经元的分隔培养物来研究其对慢速轴突运输的影响。将BFA(1微克/毫升)施加于细胞体/近端轴突6至20小时,会破坏高尔基体,可逆地阻断轴突生长,并可逆地阻断包括微管蛋白在内的所有蛋白质的顺向运输。神经生长因子(NGF)的逆向运输也被阻断。用BFA处理6小时后,对NGF作出反应的Erk1和Erk2的磷酸化不受影响,这表明轴突运输的阻断是特异性和直接的。与其在高尔基体的主要作用位点一致,仅将BFA施加于远端轴突时未观察到任何影响。快速顺向和逆向轴突运输的阻断与高尔基体在提供运输小泡中的作用一致。慢速轴突运输的阻断令人惊讶,进一步的结果表明,通过将BFA施加于细胞体,沿轴突途中的微管蛋白运输会被阻止,这表明需要从高尔基体持续供应顺向运输小泡来维持细胞骨架蛋白的慢速轴突运输。