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人海马突触周隙星形胶质细胞的三维关系。

Three-dimensional relationships between perisynaptic astroglia and human hippocampal synapses.

机构信息

Medical College of Georgia, Augusta, Georgia, USA.

出版信息

Glia. 2010 Apr;58(5):572-87. doi: 10.1002/glia.20946.

Abstract

Perisynaptic astroglia are critical for normal synaptic development and function. Little is known, however, about perisynaptic astroglia in the human hippocampus. When mesial temporal lobe epilepsy (MTLE) is refractory to medication, surgical removal is required for seizure quiescence. To investigate perisynaptic astroglia in human hippocampus, we recovered slices for several hours in vitro from three surgical specimens and then quickly fixed them to achieve high-quality ultrastructure. Histological samples from each case were found to have mesial temporal sclerosis with Blumcke Type 1a (mild, moderate) or 1b (severe) pathology. Quantitative analysis through serial section transmission electron microscopy in CA1 stratum radiatum revealed more synapses in the mild (10/10 microm(3)) than the moderate (5/10 microm(3)) or severe (1/10 microm(3)) cases. Normal spines occurred in mild and moderate cases, but a few multisynaptic spines were all that remained in the severe case. Like adult rat hippocampus, perisynaptic astroglial processes were preferentially associated with larger synapses in the mild and moderate cases, but rarely penetrated the cluster of axonal boutons surrounding multisynaptic spines. Synapse perimeters were only partially surrounded by astroglial processes such that all synapses had some access to substances in the extracellular space, similar to adult rat hippocampus. Junctions between astroglial processes were observed more frequently in moderate than mild case, but were obscured by densely packed intermediate filaments in astroglial processes of the severe case. These findings suggest that perisynaptic astroglial processes associate with synapses in human hippocampus in a manner similar to model systems and are disrupted by severe MTLE pathology.

摘要

突触旁星形胶质细胞对于正常的突触发育和功能至关重要。然而,关于人类海马体中的突触旁星形胶质细胞知之甚少。当内侧颞叶癫痫(MTLE)对药物治疗无效时,需要手术切除以控制癫痫发作。为了研究人类海马体中的突触旁星形胶质细胞,我们从三个手术标本中体外恢复了几个小时的切片,然后迅速固定它们以获得高质量的超微结构。发现每个病例的组织样本均有内侧颞叶硬化症,Blumcke 1a 型(轻度、中度)或 1b 型(重度)病理学。通过 CA1 放射状层的连续切片透射电子显微镜的定量分析显示,轻度(10/10 μm³)比中度(5/10 μm³)或重度(1/10 μm³)病例有更多的突触。轻度和中度病例中出现正常的棘突,但在重度病例中仅剩下几个多突触棘突。与成年大鼠海马体一样,在轻度和中度病例中,突触旁星形胶质细胞突起优先与较大的突触相关,但在重度病例中很少穿透多突触棘突周围的轴突末梢簇。突触的周长仅部分被星形胶质细胞突起包围,使得所有突触都有一些进入细胞外空间的物质,类似于成年大鼠海马体。在中度病例中观察到星形胶质细胞突起之间的连接比轻度病例更频繁,但在重度病例中被星形胶质细胞突起中密集排列的中间纤维所掩盖。这些发现表明,突触旁星形胶质细胞突起与人类海马体中的突触以类似于模型系统的方式相关联,并被严重的 MTLE 病理学破坏。

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