Guentchev M, Groschup M H, Kordek R, Liberski P P, Budka H
Austrian Reference Center for Human Prion Diseases and Institute of Neurology, University of Vienna.
Brain Pathol. 1998 Oct;8(4):615-23. doi: 10.1111/j.1750-3639.1998.tb00188.x.
Little is known about the pathogenetic basis of characteristic symptoms in transmissible spongiform encephalopathies (TSEs) such as myoclonus and characteristic EEG hyperactivity. We investigated the GABAergic system and its subpopulations in mice inoculated with experimental scrapie (ME7, RML, 22A strains) and Creutzfeldt-Jakob disease (CJD; Fujisaki strain), to study damage to inhibitory neurons. Since recent studies have shown electrophysiological changes in prion protein (PrP) knockout mice, we also studied mice lacking or overexpressing the PrP gene. Antibodies against glutamic acid decarboxylase (GAD), parvalbumin (PV), calbindin (CB), and calretinin (CR) were used to stain GABAergic neurons, and isolectin-B4 to stain perineuronal nets around PV+ neurons. In scrapie infected mice, cortical PV+ neurons were severely reduced while CB+ and CR+ neurons were well preserved. In CJD inoculated mice, loss of PV+ neurons was severe and occurred very early after inoculation. PrP-/- and tg20 mice showed normal appearance of PV, CB, CR, GAD+ neurons and their neuropil, and of isolectin-B4+ perineuronal nets. The early, severe and selective loss of cortical PV+ neurons in experimental scrapie and CJD suggest selective loss of PV+ GABAergic neurons as important event during disease development, possibly as one basis of excitatory symptoms in TSEs.
对于可传播性海绵状脑病(TSEs)如肌阵挛和特征性脑电图活动亢进等特征性症状的发病机制知之甚少。我们研究了接种实验性羊瘙痒病(ME7、RML、22A毒株)和克雅氏病(CJD;藤崎毒株)的小鼠的GABA能系统及其亚群,以研究抑制性神经元的损伤情况。由于最近的研究显示朊病毒蛋白(PrP)基因敲除小鼠存在电生理变化,我们还研究了缺乏或过度表达PrP基因的小鼠。使用抗谷氨酸脱羧酶(GAD)、小白蛋白(PV)、钙结合蛋白(CB)和钙视网膜蛋白(CR)的抗体对GABA能神经元进行染色,并用异凝集素-B4对PV+神经元周围的神经周网进行染色。在感染羊瘙痒病的小鼠中,皮质PV+神经元严重减少,而CB+和CR+神经元保存完好。在接种CJD的小鼠中,PV+神经元的丧失很严重,且在接种后很早就出现了。PrP-/-和tg20小鼠的PV、CB、CR、GAD+神经元及其神经纤维网以及异凝集素-B4+神经周网外观正常。实验性羊瘙痒病和CJD中皮质PV+神经元早期、严重且选择性的丧失表明,PV+ GABA能神经元的选择性丧失是疾病发展过程中的重要事件,可能是TSEs兴奋性症状的一个基础。