Jasińska Magdalena, Miłek Jacek, Cymerman Iwona A, Łęski Szymon, Kaczmarek Leszek, Dziembowska Magdalena
Laboratory of Neurobiology, The Nencki Institute, Pasteura 3, 02-093, Warsaw, Poland.
Laboratory of Molecular Basis of Synaptic Plasticity, Center of New Technologies, University of Warsaw, Warsaw, Poland.
Mol Neurobiol. 2016 Sep;53(7):4701-12. doi: 10.1007/s12035-015-9383-z. Epub 2015 Aug 29.
Mir-132 is a neuronal activity-regulated microRNA that controls the morphology of dendritic spines and neuronal transmission. Similar activities have recently been attributed to matrix metalloproteinase-9 (MMP-9), an extrasynaptic protease. In the present study, we provide evidence that miR-132 directly regulates MMP-9 mRNA in neurons to modulate synaptic plasticity. With the use of luciferase reporter system, we show that miR-132 binds to the 3'UTR of MMP-9 mRNA to regulate its expression in neurons. The overexpression of miR-132 in neurons reduces the level of endogenous MMP-9 protein secretion. In synaptoneurosomes, metabotropic glutamate receptor (mGluR)-induced signaling stimulates the dissociation of miR-132 from polyribosomal fractions and shifts it towards the messenger ribonucleoprotein (mRNP)-containing fraction. Furthermore, we demonstrate that the overexpression of miR-132 in the cultured hippocampal neurons from Fmr1 KO mice that have increased synaptic MMP-9 level provokes enlargement of the dendritic spine heads, a process previously implicated in enhanced synaptic plasticity. We propose that activity-dependent miR-132 regulates structural plasticity of dendritic spines through matrix metalloproteinase 9.
Mir-132是一种受神经元活动调节的微小RNA,它控制树突棘的形态和神经元传递。最近,类似的活动也被归因于细胞外基质金属蛋白酶9(MMP-9),一种突触外蛋白酶。在本研究中,我们提供证据表明miR-132直接调节神经元中的MMP-9 mRNA以调节突触可塑性。通过使用荧光素酶报告系统,我们表明miR-132与MMP-9 mRNA的3'UTR结合以调节其在神经元中的表达。神经元中miR-132的过表达降低了内源性MMP-9蛋白的分泌水平。在突触神经小体中,代谢型谷氨酸受体(mGluR)诱导的信号传导刺激miR-132从多核糖体组分中解离,并使其向含有信使核糖核蛋白(mRNP)的组分转移。此外,我们证明,在具有增加的突触MMP-9水平的Fmr1基因敲除小鼠的培养海马神经元中,miR-132的过表达会引起树突棘头部的增大,这一过程先前与增强的突触可塑性有关。我们提出,活动依赖性miR-132通过基质金属蛋白酶9调节树突棘的结构可塑性。