Kim C H, Lisman J E
Department of Neuroscience and Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, USA.
J Neurosci. 1999 Jun 1;19(11):4314-24. doi: 10.1523/JNEUROSCI.19-11-04314.1999.
The role of actin filaments in synaptic function has been studied in the CA1 region of the rat hippocampal slice. Bath application (2 hr) of the actin polymerization inhibitor latrunculin B did not substantially affect the shape of dendrites or spines. However, this and other drugs that affect actin did affect synaptic function. Bath-applied latrunculin B reduced the synaptic response. Several lines of evidence indicate that a component of this effect is presynaptic. To specifically test for a postsynaptic role for actin, latrunculin B or phalloidin, an actin filament stabilizer, was perfused into the postsynaptic neuron. The magnitude of long-term potentiation (LTP) was decreased at times when baseline transmission was not yet affected. Longer applications produced a decrease in baseline AMPA receptor (AMPAR)-mediated transmission. The magnitude of the NMDA receptor-mediated transmission was unaffected, indicating a specific effect on the AMPAR. These results suggest that postsynaptic actin filaments are involved in a dynamic process required to maintain AMPAR-mediated transmission and to enhance it during LTP.
肌动蛋白丝在突触功能中的作用已在大鼠海马切片的CA1区进行了研究。浴加(2小时)肌动蛋白聚合抑制剂拉特罗毒素B对树突或棘的形状没有实质性影响。然而,这种以及其他影响肌动蛋白的药物确实影响了突触功能。浴加拉特罗毒素B降低了突触反应。几条证据表明,这种效应的一个成分是突触前的。为了专门测试肌动蛋白在突触后的作用,将拉特罗毒素B或肌动蛋白丝稳定剂鬼笔环肽灌注到突触后神经元中。在基线传递尚未受到影响时,长期增强(LTP)的幅度降低。更长时间的应用导致基线AMPA受体(AMPAR)介导的传递减少。NMDA受体介导的传递幅度未受影响,表明对AMPAR有特定作用。这些结果表明,突触后肌动蛋白丝参与了维持AMPAR介导的传递以及在LTP期间增强该传递所需的动态过程。