Smith Alexander C W, Scofield Michael D, Kalivas Peter W
Department of Neuroscience, Medical University of South Carolina, Charleston, SC 29425, United States.
Department of Neuroscience, Medical University of South Carolina, Charleston, SC 29425, United States.
Brain Res. 2015 Dec 2;1628(Pt A):29-39. doi: 10.1016/j.brainres.2015.03.027. Epub 2015 Mar 30.
Synaptic plasticity has long been known to involve three key elements of neuropil, the presynapse, the postsynapse and adjacent glia. Here we review the role of the extracellular matrix in synaptic plasticity as a necessary component forming the tetrapartite synapse. We describe the role of matrix metalloproteinases as enzymes sculpting extracellular proteins and thereby creating an extracellular signaling domain required for synaptic plasticity. Specifically we focus on the role of the tetrapartite synapse in mediating the effects of addictive drugs at cortico-striatal synapses, and conclude that the extracellular signaling domain and its regulation by matrix metalloproteinases is critical for developing and expressing drug seeking behaviors.
长期以来,人们一直认为突触可塑性涉及神经毡的三个关键要素,即突触前膜、突触后膜和相邻的神经胶质细胞。在这里,我们回顾细胞外基质在突触可塑性中的作用,它是形成四联突触的必要组成部分。我们描述了基质金属蛋白酶作为塑造细胞外蛋白质的酶的作用,从而创造出突触可塑性所需的细胞外信号域。具体而言,我们关注四联突触在介导成瘾药物对皮质-纹状体突触的作用中的作用,并得出结论,细胞外信号域及其由基质金属蛋白酶的调节对于发展和表达觅药行为至关重要。