Ramachandran Binu, Frey Julietta U
Department of Neurophysiology, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany.
J Neurosci. 2009 Sep 30;29(39):12167-73. doi: 10.1523/JNEUROSCI.2045-09.2009.
Long-term potentiation (LTP) is a cellular correlate for memory formation, which requires the dynamic changes of the actin cytoskeleton. As shown by others, the polymerization of the actin network is important for early stages of LTP. Here, we investigated the role of actin dynamics in synaptic tagging and particularly in the induction of protein synthesis-dependent late-LTP in the CA1 region in hippocampal slices in vitro. We found that the inhibition of actin polymerization affects protein synthesis-independent early-LTP, prevents late-LTP, and interferes with synaptic tagging in apical dendrites of hippocampal CA1. The transformation of early-LTP into late-LTP was blocked by the application of the structurally different actin polymerization inhibitors latrunculin A or cytochalasin D. We suggest that the actin network is required for early "housekeeping" processes to induce and maintain early-LTP. Furthermore, inhibition of actin dynamics negatively interacts with the setting of the synaptic tagging complex. We propose actin as a further tag-specific molecule in apical CA1 dendrites where it is directly involved in the tagging/capturing machinery. Consequently, inhibition of the actin network prevents the interaction of tagging complexes with plasticity-related proteins. This results in the prevention of late-LTP by inhibition of the actin network during LTP induction.
长时程增强(LTP)是记忆形成的细胞关联物,它需要肌动蛋白细胞骨架的动态变化。正如其他人所表明的,肌动蛋白网络的聚合对于LTP的早期阶段很重要。在这里,我们研究了肌动蛋白动力学在突触标记中的作用,特别是在体外海马切片CA1区蛋白合成依赖性晚期LTP的诱导中的作用。我们发现,肌动蛋白聚合的抑制影响蛋白合成非依赖性早期LTP,阻止晚期LTP,并干扰海马CA1顶树突中的突触标记。应用结构不同的肌动蛋白聚合抑制剂Latrunculin A或细胞松弛素D可阻止早期LTP向晚期LTP的转变。我们认为,肌动蛋白网络对于诱导和维持早期LTP的早期“管家”过程是必需的。此外,肌动蛋白动力学的抑制与突触标记复合体的设置产生负相互作用。我们提出肌动蛋白是顶CA1树突中另一种标记特异性分子,它直接参与标记/捕获机制。因此,肌动蛋白网络的抑制阻止了标记复合体与可塑性相关蛋白的相互作用。这导致在LTP诱导期间通过抑制肌动蛋白网络来阻止晚期LTP。