Sinden J D, Rashid-Doubell F, Kershaw T R, Nelson A, Chadwick A, Jat P S, Noble M D, Hodges H, Gray J A
Neurodegeneration Research Group, Institute of Psychiatry, London, U.K.
Neuroscience. 1997 Dec;81(3):599-608. doi: 10.1016/s0306-4522(97)00330-8.
Transient global cerebral ischaemia in rats causes relatively circumscribed and specific damage to the CA1 pyramidal cells of the dorsal hippocampus, along with a cognitive deficit manifest as difficulties in the performance of a range of spatial learning and memory tasks. Our previous studies have shown that restoration of behavioural performance in ischaemic rats by neural grafts taken relatively late in fetal development occurs only after local replacement of cells homotypic to those lost through the ischaemic insult. This lesion-plus-behaviour model therefore offers a powerful means for establishing whether multipotent embryonic neuroepithelial cells will engraft the damaged CA1, develop into appropriate neuronal phenotypes and produce behavioural recovery. Here we report that, in rats subjected to 15 min of global cerebral ischaemia, intrahippocampal implants of a conditionally immortal, multipotent cell line, directly derived from the embryonic day 14 hippocampal neuroepithelium of the H-2Kb-tsA58 transgenic mouse, selectively repopulated the lesioned CA1 pyramidal layer and restored ischaemia-induced deficits in acquisition of a hidden platform location in the Morris water maze.
大鼠短暂性全脑缺血会对背侧海马体的CA1锥体细胞造成相对局限且特定的损伤,同时还会导致认知缺陷,表现为在一系列空间学习和记忆任务的执行中存在困难。我们之前的研究表明,在胎儿发育后期取自胎儿的神经移植物恢复缺血大鼠的行为表现,仅在局部替换因缺血损伤而丢失的同型细胞后才会发生。因此,这种损伤加行为模型为确定多能胚胎神经上皮细胞是否会植入受损的CA1、发育成适当的神经元表型并产生行为恢复提供了一种强大的手段。在此我们报告,在经历15分钟全脑缺血的大鼠中,将直接源自H-2Kb-tsA58转基因小鼠胚胎第14天海马神经上皮的条件永生多能细胞系植入海马内,可选择性地重新填充受损的CA1锥体细胞层,并恢复缺血诱导的在莫里斯水迷宫中获取隐藏平台位置的缺陷。