病毒感染朊病毒病小鼠会加剧小胶质细胞的炎症反应。

Virus Infections on Prion Diseased Mice Exacerbate Inflammatory Microglial Response.

作者信息

Lins Nara, Mourão Luiz, Trévia Nonata, Passos Aline, Farias José Augusto, Assunção Jarila, Quintairos Amanda, Bento-Torres João, Consentino Kronka Sosthenes Marcia, Diniz José Antonio Picanço, Vasconcelos Pedro Fernando da Costa, Picanço-Diniz Cristovam Wanderley

机构信息

Universidade Federal do Pará, Instituto de Ciências Biológicas, Laboratório de Investigações em Neurodegeneração e Infecção no Hospital Universitário João de Barros Barreto, Belém, Brazil.

Instituto Evandro Chagas, Laboratório de Microscopia Eletrônica and Departamento de Arbovirologia e Febres Hemorrágicas Virais, Belém, Brazil.

出版信息

Oxid Med Cell Longev. 2016;2016:3974648. doi: 10.1155/2016/3974648. Epub 2016 Nov 27.

Abstract

We investigated possible interaction between an arbovirus infection and the ME7 induced mice prion disease. C57BL/6, females, 6-week-old, were submitted to a bilateral intrahippocampal injection of ME7 prion strain (ME7) or normal brain homogenate (NBH). After injections, animals were organized into two groups: NBH ( = 26) and ME7 ( = 29). At 15th week after injections (wpi), animals were challenged intranasally with a suspension of Piry arbovirus 0.001% or with NBH. Behavioral changes in ME7 animals appeared in burrowing activity at 14 wpi. Hyperactivity on open field test, errors on rod bridge, and time reduction in inverted screen were detected at 15th, 19th, and 20th wpi respectively. Burrowing was more sensitive to earlier hippocampus dysfunction. However, Piry-infection did not significantly affect the already ongoing burrowing decline in the ME7-treated mice. After behavioral tests, brains were processed for IBA1, protease-resistant form of PrP, and Piry virus antigens. Although virus infection in isolation did not change the number of microglia in CA1, virus infection in prion diseased mice (at 17th wpi) induced changes in number and morphology of microglia in a laminar-dependent way. We suggest that virus infection exacerbates microglial inflammatory response to a greater degree in prion-infected mice, and this is not necessarily correlated with hippocampal-dependent behavioral deficits.

摘要

我们研究了虫媒病毒感染与ME7诱导的小鼠朊病毒病之间可能存在的相互作用。选用6周龄雌性C57BL/6小鼠,双侧海马内注射ME7朊病毒株(ME7)或正常脑匀浆(NBH)。注射后,将动物分为两组:NBH组(n = 26)和ME7组(n = 29)。注射后第15周(wpi),给动物经鼻内注射0.001%的Piry虫媒病毒悬液或NBH。ME7组动物在注射后第14周时,在掘洞行为上出现行为变化。在第15周、第19周和第20周时,分别检测到旷场试验中的多动、杆式桥梁试验中的错误以及倒屏试验中的时间减少。掘洞行为对早期海马功能障碍更为敏感。然而,Piry病毒感染并未显著影响ME7处理小鼠中已经持续的掘洞行为下降。行为测试后,对大脑进行处理,以检测IBA1、抗蛋白酶形式的PrP和Piry病毒抗原。虽然单独的病毒感染并未改变CA1区小胶质细胞的数量,但朊病毒病小鼠(在第17周wpi)中的病毒感染以层依赖的方式诱导了小胶质细胞数量和形态的变化。我们认为,病毒感染在朊病毒感染小鼠中更严重地加剧了小胶质细胞的炎症反应,而这不一定与海马依赖的行为缺陷相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab38/5149707/4cb2a04bbabd/OMCL2016-3974648.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索