Faissner Andreas, Pyka Martin, Geissler Maren, Sobik Thomas, Frischknecht Renato, Gundelfinger Eckart D, Seidenbecher Constanze
Department of Cell Morphology and Molecular Neurobiology, Ruhr-University, D-44801 Bochum, Germany.
Brain Res Rev. 2010 May;63(1-2):26-38. doi: 10.1016/j.brainresrev.2010.01.001. Epub 2010 Jan 21.
The concept of the tripartite synapse proposes that in addition to the presynapse and the postsynaptic membrane closely apposed processes of astrocytes constitute an integral part of the synapse. Accordingly, astrocytes may influence synaptic activity by various ways. Thus glia- and neuron-derived neurotrophins, cytokines and metabolites influence neuronal survival, synaptic activity and plasticity. Beyond these facts, the past years have shown that astrocytes are required for synaptogenesis, the structural maintenance and proper functioning of synapses. In particular, astrocytes seem to play a key role in the organization of the brain's extracellular matrix (ECM) - most prominently the so-called perineuronal nets (PNNs), complex macromolecular assemblies of ECM components. Due to progress in cellular and molecular neurosciences, it has been possible to decipher the composition of ECM structures and to obtain insight into their function(s) and underlying mechanisms. It appears that PNN-related structures are involved in regulating the sprouting and pruning of synapses, which represents an important morphological correlate of synaptic plasticity in the adult nervous system. Perturbation assays and gene elimination by recombinant techniques have provided clear indications that astrocyte-derived ECM components, e.g. the tenascins and chondroitinsulfate proteoglycans (CSPGs) of the lectican family participate in these biological functions. The present review will discuss the glia-derived glycoproteins and CSPGs of the perisynaptic ECM, their neuronal and glial receptors, and in vitro assays to test their physiological functions in the framework of the synapse, the pivotal element of communication in the central nervous system.
三联突触的概念提出,除了突触前膜和紧密相邻的突触后膜外,星形胶质细胞的相关过程也构成了突触的一个组成部分。因此,星形胶质细胞可能通过多种方式影响突触活动。神经胶质细胞和神经元来源的神经营养因子、细胞因子和代谢产物会影响神经元的存活、突触活动和可塑性。除了这些事实,过去几年的研究表明,星形胶质细胞对于突触形成、突触的结构维持和正常功能是必需的。特别是,星形胶质细胞似乎在大脑细胞外基质(ECM)的组织中起着关键作用——最显著的是所谓的神经元周围网(PNN),它是ECM成分的复杂大分子集合体。由于细胞和分子神经科学的进展,已经能够解析ECM结构的组成,并深入了解其功能和潜在机制。似乎与PNN相关的结构参与调节突触的发芽和修剪,这是成年神经系统中突触可塑性的一个重要形态学关联。通过重组技术进行的扰动实验和基因剔除实验已经明确表明,星形胶质细胞衍生的ECM成分,例如富含亮氨酸蛋白聚糖家族的腱糖蛋白和硫酸软骨素蛋白聚糖(CSPG)参与了这些生物学功能。本综述将讨论突触周围ECM中神经胶质细胞衍生的糖蛋白和CSPG、它们的神经元和神经胶质细胞受体,以及在突触框架内测试其生理功能的体外实验,突触是中枢神经系统通讯的关键要素。