首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Experimental herpes simplex virus encephalitis: a long-term study of interleukin-6 expression in mouse brain tissue.
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Experimental herpes simplex virus encephalitis: a long-term study of interleukin-6 expression in mouse brain tissue.

机译:实验性单纯疱疹病毒性脑炎:小鼠脑组织中白介素6表达的长期研究。

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摘要

This study aimed to investigate the expression of interleukin-6 (IL-6) in acute and chronic herpes simplex virus encephalitis. In the brain of 15 SJL mice infected with herpes simplex virus type 1, strain F, and 14 control animals we performed a sequential quantitative analysis of expression of IL-6 mRNA with reverse transcription real-time polymerase chain reaction. The viral burden peaked in the acute disease, and then returned to a low baseline value. At day 7 following infection, IL-6 expression was significantly (2.05-fold) increased as compared with the baseline expression in uninfected animals. Twenty-one days after infection the mRNA expression still was significantly (1.78-fold) upregulated. No significant differences of IL-6 mRNA expression between infected and control mice were found after 2 and 6 months. We observed a 2.5-fold increase of IL-6 mRNA expression in control mice with increasing age of animals. We have additionally studied the clinical evolution of HSVE in IL-6 deficient mice. In experimental herpes simplex virus encephalitis IL-6, as a potent mediator of neuronal injury, is upregulated in the acute but not in the chronic disease. IL-6 deficient mice presented early and severe clinical signs of HSVE as compared to the wild-type C57/bl6 mice.
机译:这项研究旨在调查白介素6(IL-6)在急慢性单纯疱疹病毒性脑炎中的表达。在15只感染了单纯疱疹病毒1型,F株和14只对照动物的SJL小鼠的大脑中,我们进行了具有逆转录实时聚合酶链反应的IL-6 mRNA表达的顺序定量分析。病毒载量在急性疾病中达到峰值,然后又回到较低的基线值。感染后第7天,与未感染动物的基线表达相比,IL-6表达显着提高(2.05倍)。感染后二十一天,mRNA表达仍显着上调(1.78倍)。 2个月和6个月后,在感染小鼠和对照小鼠之间没有发现IL-6 mRNA表达的显着差异。我们观察到,随着动物年龄的增长,对照小鼠中IL-6 mRNA表达增加了2.5倍。我们还研究了IL-6缺陷小鼠中HSVE的临床演变。在实验性单纯疱疹病毒性脑炎中,IL-6作为神经元损伤的有效介体,在急性疾病中被上调,而在慢性疾病中则不被上调。与野生型C57 / bl6小鼠相比,IL-6缺陷小鼠表现出早期和严重的HSVE临床症状。

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