首页> 外文OA文献 >Human Immunodeficiency Virus Type 1 Infection Increases the In Vivo Capacity of Peripheral Monocytes To Cross the Blood-Brain Barrier into the Brain and the In Vivo Sensitivity of the Blood-Brain Barrier to Disruption by Lipopolysaccharide▿
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Human Immunodeficiency Virus Type 1 Infection Increases the In Vivo Capacity of Peripheral Monocytes To Cross the Blood-Brain Barrier into the Brain and the In Vivo Sensitivity of the Blood-Brain Barrier to Disruption by Lipopolysaccharide▿

机译:1型人类免疫缺陷病毒感染会增加外周单核细胞穿过血脑屏障进入大脑的体内能力,以及血脂屏障对脂多糖破坏的体内敏感性▿

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摘要

Human immunodeficiency virus type 1 (HIV-1), introduced into the brain by HIV-1-infected monocytes which migrate across the blood-brain barrier (BBB), infects resident macrophages and microglia and initiates a process that causes HIV-1-associated neurocognitive disorders. The mechanism by which HIV-1 infection circumvents the BBB-restricted passage of systemic leukocytes into the brain and disrupts the integrity of the BBB is not known. Circulating lipopolysaccharide (LPS), which can compromise the integrity of the BBB, is significantly increased in HIV-1-infected individuals. We hypothesized that HIV-1 infection increases monocyte capacity to migrate across the BBB, which is further facilitated by a compromise of BBB integrity mediated by the increased systemic LPS levels present in HIV-1-infected individuals. To investigate this possibility, we examined the in vivo BBB migration of monocytes derived from our novel mouse model, JR-CSF/EYFP mice, which are transgenic for both a long terminal repeat-regulated full-length infectious HIV-1 provirus and ROSA-26-regulated enhanced yellow fluorescent protein. We demonstrated that JR-CSF/EYFP mouse monocytes displayed an increased capacity to enter the brain by crossing either an intact BBB or a BBB whose integrity was partially compromised by systemic LPS. We also demonstrated that the JR-CSF mouse BBB was more susceptible to disruption by systemic LPS than the control wild-type mouse BBB. These results demonstrated that HIV-1 infection increased the ability of monocytes to enter the brain and increased the sensitivity of the BBB to disruption by systemic LPS, which is elevated in HIV-1-infected individuals. These mice represent a new in vivo system for studying the mechanism by which HIV-1-infected monocytes migrate into the brain.
机译:人类免疫缺陷病毒1型(HIV-1),是由被HIV-1感染的单核细胞跨血脑屏障(BBB)迁移而进入大脑的,它会感染常驻巨噬细胞和小胶质细胞,并引发导致与HIV-1相关的过程神经认知障碍。 HIV-1感染绕过BBB限制的全身白细胞进入大脑并破坏BBB完整性的机制尚不清楚。可以损害BBB完整性的循环脂多糖(LPS)在感染HIV-1的个体中显着增加。我们假设HIV-1感染会增加单核细胞跨BBB迁移的能力,这进一步受到感染HIV-1的个体体内系统性LPS水平升高介导的BBB完整性损害的进一步促进。为了研究这种可能性,我们检查了源自我们新颖的小鼠模型JR-CSF / EYFP小鼠的单核细胞的体内BBB迁移,这些小鼠对长末端重复调控的全长传染性HIV-1前病毒和ROSA- 26调节的增强型黄色荧光蛋白。我们证明,JR-CSF / EYFP小鼠单核细胞通过穿越完整的BBB或完整性受到系统性LPS损害的BBB表现出增加的进入大脑的能力。我们还证明,与对照野生型小鼠BBB相比,JR-CSF小鼠BBB更容易受到系统性LPS的破坏。这些结果表明,HIV-1感染增加了单核细胞进入大脑的能力,并增加了BBB对全身性LPS破坏的敏感性,而在感染HIV-1的个体中,LPS升高。这些小鼠代表了一种新的体内系统,用于研究感染HIV-1的单核细胞迁移到大脑的机制。

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