Okazaki M M, Evenson D A, Nadler J V
Department of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Comp Neurol. 1995 Feb 20;352(4):515-34. doi: 10.1002/cne.903520404.
In complex partial epilepsy and in animal models of epilepsy, hippocampal mossy fibers appear to develop recurrent collaterals that invade the dentate molecular layer. Mossy fiber collaterals have been proposed to subserve recurrent excitation by forming granule cell-granule cell synapses. This hypothesis was tested by visualizing dentate granule cells and their mossy fibers after terminal uptake and retrograde transport of biocytin. Labeling studies were performed with transverse slices of the caudal rat hippocampal formation prepared 2.6-70.0 weeks after pilocarpine-induced or kainic acid-induced status epilepticus. Light microscopy demonstrated the progressive growth of recurrent mossy fibers into the molecular layer; the densest innervation was observed in slices from pilocarpine-treated rats that had survived 10 weeks or longer after status epilepticus. Thin mossy fiber collaterals originated predominantly from deep within the hilar region, crossed the granule cell body layer, and formed an axonal plexus oriented parallel to the cell body layer within the inner one-third of the molecular layer. When sprouting was most robust, some recurrent mossy fibers at the apex of the dentate gyrus reached the outer two-thirds of the molecular layer. The distribution and density of mossy fiber-like Timm staining correlated with the biocytin labeling. When viewed with the electron microscope, the inner one-third of the dentate molecular layer contained numerous mossy fiber boutons. In some instances, biocytin-labeled mossy fiber boutons were engaged in synaptic contact with biocytin-labeled granule cell dendrites. Granule cell dendrites did not develop large complex spines ("thorny excrescences") at the site of synapse formation, and they did not appear to have been permanently damaged by seizure activity. These results establish the validity of Timm staining as a marker for mossy fiber sprouting and support the view that status epilepticus provokes the formation of a novel recurrent excitatory circuit in the dentate gyrus. Retrograde labeling with biocytin showed that the recurrent mossy fiber projection often occupies a considerably greater fraction of the dendritic region than previous studies had suggested.
在复杂部分性癫痫及癫痫动物模型中,海马苔藓纤维似乎会形成反复分支并侵入齿状分子层。有人提出苔藓纤维分支通过形成颗粒细胞-颗粒细胞突触来实现反复兴奋。通过在生物胞素终末摄取和逆行转运后观察齿状颗粒细胞及其苔藓纤维,对这一假说进行了验证。对匹罗卡品或 kainic 酸诱导癫痫持续状态后 2.6 - 70.0 周制备的大鼠尾侧海马结构横切片进行标记研究。光学显微镜显示反复的苔藓纤维逐渐生长进入分子层;在癫痫持续状态后存活 10 周或更长时间的匹罗卡品处理大鼠的切片中观察到最密集的神经支配。细小的苔藓纤维分支主要起源于海马门区深处,穿过颗粒细胞体层,并在分子层内三分之一处形成与细胞体层平行的轴突丛。当发芽最旺盛时,齿状回顶端的一些反复苔藓纤维到达分子层外三分之二处。苔藓纤维样 Timm 染色的分布和密度与生物胞素标记相关。在电子显微镜下观察,齿状分子层的内三分之一包含大量苔藓纤维终扣。在某些情况下,生物胞素标记的苔藓纤维终扣与生物胞素标记的颗粒细胞树突形成突触接触。颗粒细胞树突在突触形成部位未形成大的复杂棘突(“棘状赘生物”),且似乎未因癫痫活动而受到永久性损伤。这些结果证实了 Timm 染色作为苔藓纤维发芽标记物的有效性,并支持癫痫持续状态在齿状回引发新的反复兴奋性回路形成的观点。用生物胞素进行逆行标记显示,反复的苔藓纤维投射通常占据的树突区域比例比以往研究表明的要大得多。