Yamazaki M, Matsuo R, Fukazawa Y, Ozawa F, Inokuchi K
Mitsubishi Kagaku Institute of Life Sciences, Minamiooya, Machida, Tokyo, Japan.
J Neurochem. 2001 Oct;79(1):192-9. doi: 10.1046/j.1471-4159.2001.00552.x.
We report NMDA receptor-dependent expression of synaptopodin mRNA in the dentate granule cells of the hippocampus following induction of long-term potentiation (LTP) in vivo. Synaptopodin did not belong to immediate-early genes, as de novo protein synthesis was required for the induction of synaptopodin gene transcription. An increased level of synaptopodin mRNA was observed at 75 min and 3.5 h after the onset of LTP. Importantly, there was correlation between the induction of mRNA expression and the persistence of LTP. Synaptopodin immunoreactivity was elevated specifically in synaptic layers, middle and outer molecular layers of dentate gyrus where LTP was induced. As synaptopodin is an actin-associated protein present in spine neck and implicated in the modulation of cell morphology, our results suggest that synaptopodin, by regulating the dynamics of the actin cytoskeleton, contributes to the morphological change in spine shape considered to be important for the maintenance of synaptic plasticity.
我们报道了在体内诱导长时程增强(LTP)后,海马齿状颗粒细胞中突触素mRNA的NMDA受体依赖性表达。突触素不属于即早基因,因为突触素基因转录的诱导需要从头合成蛋白质。在LTP开始后75分钟和3.5小时观察到突触素mRNA水平升高。重要的是,mRNA表达的诱导与LTP的持续性之间存在相关性。在诱导LTP的齿状回的突触层、中层和外分子层中,突触素免疫反应性特异性升高。由于突触素是一种存在于棘突颈部的肌动蛋白相关蛋白,与细胞形态的调节有关,我们的结果表明,突触素通过调节肌动蛋白细胞骨架的动力学,有助于棘突形状的形态变化,这被认为对维持突触可塑性很重要。