Cantallops I, Routtenberg A
Cresap Neuroscience Laboratory, Northwestern University Institute for Neuroscience, Northwestern University, Evanston, Illinois, USA.
Hippocampus. 2000;10(3):269-73. doi: 10.1002/1098-1063(2000)10:3<269::AID-HIPO7>3.0.CO;2-R.
After seizures caused by kindling or kainic acid (KA), hippocampal granule-cell axons, the mossy fibers, sprout into the supragranular layer of the rat. The mechanisms underlying this phenomenon remain elusive, but excitotoxic loss of hilar cells, which project to this supragranular layer, is suspected to be a critical determinant. Consistent with this hypothesis, we previously reported that while rats show mossy fiber sprouting after kainate, ICR mice do not. This may be associated with the observation that ICR mice, unlike rats, do not appear to show hilar cell death after KA (McNamara et al., Mol Brain Res 1996;40:177-187). Other strains of mice, however, such as 129/SvEMS, do show hilar cell death after KA (Schauwecker and Steward, Proc Natl Acad Sci USA 1997;94:4103-4108). We examined the possibility that the 129/SvEMS mouse strain would show granule-cell sprouting, in contrast to ICR mice. After administration of KA, mossy fiber sprouting was indeed observed in strain 129/SvEMS, but only in animals displaying evident hilar cell death. In contrast, neither hilar cell death nor mossy fiber sprouting was observed in ICR mice, confirming previous results. Both mouse strains demonstrated comparable behavioral seizures. These results strengthen the view that hilar cell death, together with epileptogenesis, triggers reactive synaptogenesis and mossy fiber sprouting.
在由点燃或 kainic 酸(KA)引发癫痫发作后,海马颗粒细胞轴突,即苔藓纤维,会向大鼠的颗粒上层发芽。这种现象背后的机制仍然难以捉摸,但怀疑投射到该颗粒上层的门区细胞的兴奋性毒性丧失是一个关键决定因素。与这一假设一致,我们之前报道过,虽然大鼠在注射海藻酸后会出现苔藓纤维发芽,但 ICR 小鼠却不会。这可能与以下观察结果有关:与大鼠不同,ICR 小鼠在注射 KA 后似乎不会出现门区细胞死亡(McNamara 等人,《分子脑研究》1996 年;40:177 - 187)。然而,其他品系的小鼠,如 129/SvEMS,在注射 KA 后确实会出现门区细胞死亡(Schauwecker 和 Steward,《美国国家科学院院刊》1997 年;94:4103 - 4108)。我们研究了 129/SvEMS 小鼠品系与 ICR 小鼠相比是否会出现颗粒细胞发芽的可能性。注射 KA 后,确实在 129/SvEMS 品系中观察到了苔藓纤维发芽,但仅在表现出明显门区细胞死亡的动物中出现。相比之下,在 ICR 小鼠中既未观察到门区细胞死亡也未观察到苔藓纤维发芽,这证实了之前的结果。两种小鼠品系都表现出相当的行为性癫痫发作。这些结果强化了这样一种观点,即门区细胞死亡与癫痫发生一起触发了反应性突触形成和苔藓纤维发芽。