Regulation of synaptic plasticity by microRNAs

神经细胞通过称为突触的特殊细胞间连接相互交流。突触的修饰是发生在发育和学习过程中的可塑性的一个关键特征。被广泛研究的脊椎动物可塑性的例子是长期增强（LTP，一种持续的突触增强）和长期抑制（LTD，一种持续的突触减弱）。虽然可塑性中的短期事件是由蛋白质修饰介导的，但后期事件需要突触合成新的蛋白质。某些信使rna被转运到突触并在突触上翻译，这一发现导致了长期可塑性是通过空间和暂时限制蛋白质合成来实现的概念。然而，这种现象发生的分子基础仍然难以捉摸。MicroRNAs是最近发现的一类核酸，越来越被认为是蛋白质合成的关键调节因子。提示，神经元中的mirna可以在突触附近检测到。为了进一步阐明mirna在突触可塑性过程中蛋白质合成中的作用，我们想分析LTP或LTD后树突中的microRNA含量是否会发生变化。识别在可塑性过程中受调控的microrna，阐明突触中蛋白质合成的控制机制，将极大地增强我们对神经元发育以及学习和记忆的基本机制的认识。

Nerve cells communicate with each other via specialized intercellular junctions known as synapses. The modification of synapses is a key feature underlying plasticity that occurs during development and learning. Widely studied examples of vertebrate plasticity are long-term potentiation (LTP, a persistent synaptic enhancement) and long-term depression (LTD, a persistent synaptic weakening). While short-term events in plasticity are mediated by protein modifications, later events require the synthesis of new proteins at the synapse. The finding that certain messenger RNAs are transported to and translated at the synapse led to the notion that long-term plasticity is implemented by spatially and temporarily restricted protein synthesis. However, the molecular basis of how this occurs remains elusive. MicroRNAs, a recently identified class of nucleic acids, are increasingly recognized as key regulators of protein synthesis. Suggestively, miRNAs in neurons can be detected close to synapses. To further elucidate the role of miRNAs in protein synthesis during synaptic plasticity we want to analyze whether the microRNA content in the dendrite changes after LTP or LTD. Identifying microRNAs that are regulated during plasticity and elucidating the control mechanisms for protein synthesis at the synapse will greatly enhance our knowledge of basic mechanisms underlying neuronal development as well as learning and memory.