Nishida Hideko, Okabe Shigeo
Department of Cell Biology, School of Medicine, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo ku, Tokyo 113-8519, Japan.
Brain Nerve. 2007 Jul;59(7):755-61.
Increasing evidence indicates the importance of neuron-astrocyte interaction in synaptic function. However, structural evidence is scarce compared to abundant information from electrophysiological studies. Meticulous studies using serial electron microscopic technique in hippocampal CAI and cerebellum provided the earliest knowledge about three-dimensional close relationship between synapses and glial processes. Nevertheless, morphological observation of synapse-glia interaction in live tissues is important to support the idea of astrocytic effects on synaptic transmission. Recently several methods enabled live imaging of astrocytes as well as dendritic spines in acute slices and tissues cultures. The techniques to visualize live astrocytes in brain tissues include transgenic mice (GFAP promoter-GFP), sulforhodamine 101 (SR101) application to the surface of neocortex in vivo, ballistic labeling with EGFP plasmid and recombinant viruses (Semliki Forest virus A7 or adenovirus expressing EGFP). Live astrocytes in brain tissues showed higher motility than neuronal structures in the vicinity of dendrites. Astrocytes extend or retract their numerous fine processes and change their volume or shape in a complex manner. Simultaneous observation of filopodia/spines and astrocytes revealed that filopodia/spines often contact with astrocytic processes and that they showed coordinated morphological dynamics in adult and developmental stage, suggesting possible functions of synapse-astrocyte contacts. Indeed, the local regulation of filopodial stabilization and maturation into spines by astrocytic contacts was reported. In the next step any astrocytic structural changes around mature synapses correlated with plastic change of synaptic efficacy, such as long-term potentiation, should be investigated. Structural relationship between axon terminals and astrocytic processes should also be revealed. Furthermore, in vivo time-lapse imaging of synapseastrocyte pairs will soon be accomplished, as techniques of in vivo two-photon imaging showed remarkable progress recently.
越来越多的证据表明神经元与星形胶质细胞的相互作用在突触功能中具有重要性。然而,与电生理研究的丰富信息相比,结构方面的证据却很匮乏。利用海马CAI和小脑的连续电子显微镜技术进行的细致研究,提供了关于突触与胶质细胞突起三维紧密关系的最早认知。尽管如此,对活组织中突触 - 胶质细胞相互作用的形态学观察对于支持星形胶质细胞对突触传递产生影响这一观点很重要。最近,有几种方法能够对急性脑片和组织培养中的星形胶质细胞以及树突棘进行实时成像。在脑组织中可视化活星形胶质细胞的技术包括转基因小鼠(GFAP启动子 - GFP)、将磺罗丹明101(SR101)应用于体内新皮质表面、用EGFP质粒和重组病毒(Semliki森林病毒A7或表达EGFP的腺病毒)进行弹道标记。脑组织中的活星形胶质细胞比树突附近的神经元结构具有更高的运动性。星形胶质细胞伸展或缩回其众多细小的突起,并以复杂的方式改变其体积或形状。对丝状伪足/棘和星形胶质细胞的同步观察表明,丝状伪足/棘经常与星形胶质细胞的突起接触,并且它们在成年期和发育阶段表现出协调的形态动力学,这表明突触 - 星形胶质细胞接触可能具有功能。事实上,已有报道称星形胶质细胞接触可对丝状伪足的稳定以及向棘的成熟进行局部调节。下一步应研究成熟突触周围的任何星形胶质细胞结构变化与突触效能的可塑性变化(如长时程增强)之间的相关性。轴突终末与星形胶质细胞突起之间的结构关系也应予以揭示。此外,随着体内双光子成像技术最近取得显著进展,对突触 - 星形胶质细胞对的体内延时成像将很快实现。