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ADAMTS-13 和 nNOS 表达在小反刍动物李斯特菌脑炎神经发病机制中的作用。

Role of ADAMTS-13 and nNOS expression in neuropathogenesis of listeric encephalitis of small ruminants.

机构信息

Departmant of Pathology, Faculty of Veterinary Medicine, University of Cumhuriyet , Sivas, Turkey.

Eskil Vocational High School, University of Aksaray , Eskil, Turkey.

出版信息

Biotech Histochem. 2020 Nov;95(8):584-596. doi: 10.1080/10520295.2020.1743359. Epub 2020 Apr 2.

DOI:10.1080/10520295.2020.1743359
PMID:32237909
Abstract

We investigated the expression of A disintegrin and metalloprotease with thrombospondin type I repeats-13 (ADAMTS-13) in the central nervous system (CNS), because it is related to blood-brain barrier (BBB) permeability. We also investigated 8-OHdG, caspase-3 and neuronal nitric oxide synthase (nNOS) expression for the cytotoxic effects of oxidative stress (OS) and nNOS, and their relation to apoptosis. We also investigated the neuroimmunopathology caused by . Brain tissues were obtained from 10 lambs and 10 kids with listeric meningoencephalitis, and healthy brain tissue from six lambs and six kids. Serial sections of brain were stained by hematoxylin and eosin (H & E), and using immunohistochemistry (IHC) for antigen, ADAMTS-13, 8-hydroxy-2'-deoxyguanosine (8-OHdG), nNOS and caspase-3. We found that ADAMTS-13, 8-OHdG, nNOS and caspase-3 expression in the brain was increased in infected animals compared to uninfected controls. Intense staining for 8-OHdG was observed only in neurons and glia that were exposed to OS. ADAMTS-13 was increased significantly, which may play a role in regulating and protecting BBB integrity and cells of the CNS in cases of listeric encephalitis. Increased expression of ADAMTS-13 may be critical for supporting the survival of neurons and glia. We found that -related increases in OS and nNOS, and that the associated apoptosis, may participate in neurodegeneration and neuropathology in listeric encephalitis.

摘要

我们研究了在中枢神经系统(CNS)中解整合素金属蛋白酶 13(ADAMTS-13)的表达,因为它与血脑屏障(BBB)通透性有关。我们还研究了 8-羟基脱氧鸟苷(8-OHdG)、半胱氨酸天冬氨酸蛋白酶-3(caspase-3)和神经元型一氧化氮合酶(nNOS)的表达,以研究氧化应激(OS)和 nNOS 的细胞毒性作用,及其与细胞凋亡的关系。我们还研究了李斯特菌引起的神经免疫病理学。从 10 只羔羊和 10 只幼儿李斯特菌脑膜脑炎中获得脑组织,从 6 只羔羊和 6 只幼儿中获得健康脑组织。脑组织的连续切片用苏木精和伊红(H&E)染色,并进行免疫组织化学(IHC)染色,检测抗原、ADAMTS-13、8-羟基-2'-脱氧鸟苷(8-OHdG)、nNOS 和 caspase-3。我们发现,感染李斯特菌的动物脑组织中 ADAMTS-13、8-OHdG、nNOS 和 caspase-3 的表达增加,而未感染的对照组则没有。只有暴露于 OS 的神经元和神经胶质细胞中观察到 8-OHdG 的强烈染色。ADAMTS-13 的表达显著增加,这可能在李斯特菌脑炎中发挥调节和保护 BBB 完整性和中枢神经系统细胞的作用。ADAMTS-13 的表达增加可能对支持神经元和神经胶质细胞的存活至关重要。我们发现,与 OS 和 nNOS 相关的增加,以及相关的细胞凋亡,可能参与李斯特菌脑炎中的神经退行性变和神经病理学。

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