Chrétien Fabrice, Le Pavec Gwenaelle, Vallat-Decouvelaere Anne-Valérie, Delisle Marie-Bernadette, Uro-Coste Emmanuelle, Ironside James W, Gambetti Pierluigi, Parchi Piero, Créminon Christophe, Dormont Dominique, Mikol Jacqueline, Gray Francoise, Gras Gabriel
INSERM EMI0011 and Département de Pathologie, Hôpital Henri Mondor, Assistance Publique-Hôpital de Paris, Créteil, France.
J Neuropathol Exp Neurol. 2004 Oct;63(10):1058-71. doi: 10.1093/jnen/63.10.1058.
The mechanisms of neuronal apoptosis in prion diseases are unclear. Experimental studies suggest that it may result from 2 associated mechanisms: glutamate-mediated excitotoxicity and oxidative stress. Recent studies showed that activated macrophages/microglia (AMM) express excitatory amino acid transporters (EAATs) in HIV infection, suggesting that they may play a neuroprotective role by clearing extra-cellular glutamate and producing anti-oxidant glutathione. In order to test this hypothesis in prion diseases, samples from cerebral cortex, striatum, thalamus, and cerebellum from 14 patients with Creutzfeldt-Jakob disease (8 sporadic, 2 familial, 2 iatrogenic, and 2 variant), and 4 with fatal familial insomnia (3 homozygous Met/Met at codon 129 of the PRNP gene, 1 heterozygous Met/Val), and 3 controls were immunostained for EAAT-1, GFAP, HLA-DR, CD68, IL-1, caspase 3, and PrP. In prion diseases, EAAT-1 immunopositivity was found in affected areas. Only AMM, interstitial, perivascular, perineuronal (sometimes around apoptotic neurons), or close to reactive astrocytes, expressed EAAT-1. Astrocyte EAAT-1 expression was scarcely detectable in controls and was not detected in prion disease cases. The proportion of AMM expressing EAAT-1 did not correlate with the severity of neuronal apoptosis, spongiosis, astrocytosis, microgliosis, or PrP deposition, but only with disease duration. Occasional EAAT-1 expressing AMM were found in patients with short survival, whereas diffuse EAAT-1 expression by AMM was observed in cases with long survival (24 to 33 months) that most often were heterozygous for Met/Val at codon 129 of the PRNP gene. Our findings suggest that AMM may develop a partial neuroprotective function in long-lasting prion diseases, although it does not seem to efficiently prevent neurological and neuropathological deterioration. Whether this neuroprotective function of microglia is the cause or the effect of longer survival needs to be clarified.
朊病毒疾病中神经元凋亡的机制尚不清楚。实验研究表明,它可能源于两种相关机制:谷氨酸介导的兴奋性毒性和氧化应激。最近的研究表明,在HIV感染中,活化的巨噬细胞/小胶质细胞(AMM)表达兴奋性氨基酸转运体(EAATs),这表明它们可能通过清除细胞外谷氨酸和产生抗氧化剂谷胱甘肽来发挥神经保护作用。为了在朊病毒疾病中验证这一假设,对14例克雅氏病患者(8例散发性、2例家族性、2例医源性和2例变异型)以及4例致死性家族性失眠症患者(3例PRNP基因第129密码子为纯合子Met/Met,1例为杂合子Met/Val)和3例对照的大脑皮质、纹状体、丘脑和小脑样本进行了EAAT-1、GFAP、HLA-DR、CD68、IL-1、半胱天冬酶3和PrP的免疫染色。在朊病毒疾病中,在受影响区域发现了EAAT-1免疫阳性。只有AMM、间质、血管周围、神经元周围(有时在凋亡神经元周围)或靠近反应性星形胶质细胞表达EAAT-1。在对照中几乎检测不到星形胶质细胞EAAT-1的表达,在朊病毒疾病病例中未检测到。表达EAAT-1的AMM比例与神经元凋亡、海绵状变性、星形细胞增生、小胶质细胞增生或PrP沉积的严重程度无关,仅与疾病持续时间有关。在生存期短的患者中偶尔发现表达EAAT-1的AMM,而在生存期长(24至33个月)的病例中观察到AMM弥漫性表达EAAT-1,这些病例大多在PRNP基因第129密码子处为Met/Val杂合子。我们的研究结果表明,AMM可能在持久的朊病毒疾病中发挥部分神经保护功能,尽管它似乎不能有效地预防神经和神经病理恶化。小胶质细胞的这种神经保护功能是生存期延长的原因还是结果,有待阐明。