Hsu M, Buzsáki G
Center for Molecular and Behavioral Neuroscience, Rutgers 07102.
J Neurosci. 1993 Sep;13(9):3964-79. doi: 10.1523/JNEUROSCI.13-09-03964.1993.
Much of the work on forebrain ischemia in the hippocampus has focused on the phenomenon of delayed neuronal death in CA1. It is established that dentate granule cells and CA3 pyramidal cells are resistant to ischemia. However, much less is known about interneuronal involvement in CA3 or ischemic injury in the dentate hilus other than the fact that somatostatin neurons in the latter lose their immunoreactivity. We combined two sensitive methods--heat-shock protein (HSP72) immunocytochemistry and a newly developed Gallyas silver stain for demonstrating impaired cytoskeletal elements--to investigate the extent of ischemic damage to CA3 and the dentate hilus using the four-vessel-occlusion model for inducing forebrain ischemia. HSP72-like immunoreactivity was induced in neuronal populations previously shown to be vulnerable to ischemia. In addition, a distinct subset of interneurons in CA3 was also extremely sensitive to ischemia, even more so than the CA1 pyramidal cells. These neurons are located in the stratum lucidum of CA3 and possess a very high density of dendritic spines. In silver preparations, they were among the first to be impregnated as "dark" neurons, before CA1 pyramidal cells; microglial reaction was also initiated first in the stratum lucidum of CA3. Whereas CA1 damage was most prominent in the septal half of the hippocampus, hilar and CA3 interneuronal damage had a more extensive dorsoventral distribution. Our results also show a far greater extent of damage in hilar neurons than previously reported. At least four hilar cell types were consistently compromised: mossy cells, spiny fusiform cells, sparsely spiny fusiform cells, and long-spined multipolar cells. A common denominator of the injured neurons in CA3 and the hilus was the presence of spines on their dendrites, which in large part accounted for the far greater number of mossy fiber terminals they receive than their non-spiny neighbors. We suggest that the differential vulnerability of neuronal subtypes in these two regions may be attributed to their extremely dense innervation by the mossy fibers and/or the presence of non-NMDA receptor subtypes that are highly permeable to calcium. In addition, early impairment of these spiny CA3 cells and hilar neurons after ischemia may be causal to delayed neuronal death in the CA1 pyramidal cells.
海马体中关于前脑缺血的许多研究都集中在CA1区延迟性神经元死亡的现象上。现已确定齿状颗粒细胞和CA3锥体细胞对缺血具有抗性。然而,除了齿状回门中生长抑素神经元失去免疫反应性这一事实外,关于CA3区中间神经元的参与情况或齿状回门的缺血性损伤,人们了解得要少得多。我们结合了两种灵敏的方法——热休克蛋白(HSP72)免疫细胞化学和一种新开发的用于显示细胞骨架成分受损的Gallyas银染法,使用四血管闭塞模型诱导前脑缺血,来研究CA3区和齿状回门的缺血损伤程度。HSP72样免疫反应性在先前已证明易受缺血影响的神经元群体中被诱导出来。此外,CA3区的一个独特中间神经元亚群对缺血也极其敏感,甚至比CA1锥体细胞更敏感。这些神经元位于CA3区的透明层,并且具有非常高的树突棘密度。在银染标本中,它们是最早被染成“深色”神经元的,早于CA1锥体细胞;小胶质细胞反应也首先在CA3区的透明层开始。虽然CA1区的损伤在海马体的隔区一半最为明显,但门区和CA3区中间神经元的损伤在背腹分布上更为广泛。我们的结果还显示,门区神经元的损伤程度比先前报道的要大得多。至少有四种门区细胞类型持续受到损害:苔藓细胞、棘状梭形细胞、稀疏棘状梭形细胞和长棘多极细胞。CA3区和门区受损神经元的一个共同特征是它们的树突上有棘,这在很大程度上解释了它们比无棘邻居接收的苔藓纤维终末数量多得多的原因。我们认为,这两个区域神经元亚型的不同易损性可能归因于它们受到苔藓纤维的极其密集的支配和/或存在对钙高度通透的非NMDA受体亚型。此外,缺血后这些有棘的CA3细胞和门区神经元的早期损伤可能是CA1锥体细胞延迟性神经元死亡的原因。