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血脑屏障破坏:HIV Tat 对脑微血管内皮细胞及紧密连接蛋白的影响。

Disruption of blood-brain barrier: effects of HIV Tat on brain microvascular endothelial cells and tight junction proteins.

机构信息

Department of Respiratory and Critical Care Medicine, Beijing You An Hospital, Capital Medical University, Beijing, 100069, China.

出版信息

J Neurovirol. 2023 Dec;29(6):658-668. doi: 10.1007/s13365-023-01179-3. Epub 2023 Oct 29.


DOI:10.1007/s13365-023-01179-3
PMID:37899420
Abstract

Although the widespread use of antiretroviral therapy (ART) has prolonged the life span of people living with HIV (PLWH), the incidence of HIV-associated neurocognitive disorders (HAND) in PLWH is also gradually increasing, seriously affecting the quality of life for PLWH. However, the pathogenesis of HAND has not been elucidated, which leaves HAND without effective treatment. HIV protein transactivator of transcription (Tat), as an important regulatory protein, is crucial in the pathogenesis of HAND, and its mechanism of HAND has received widespread attention. The blood-brain barrier (BBB) and its cellular component brain microvascular endothelial cells (BMVECs) play a necessary role in protecting the central nervous system (CNS), and their damage associated with Tat is a potential therapeutic target of HAND. In this review, we will study the Tat-mediated damage mechanism of the BBB and present multiple lines of evidence related to BMVEC damage caused by Tat.

摘要

尽管抗逆转录病毒疗法(ART)的广泛应用延长了艾滋病毒感染者(PLWH)的寿命,但 HIV 相关神经认知障碍(HAND)的发病率也在逐渐增加,严重影响了 PLWH 的生活质量。然而,HAND 的发病机制尚未阐明,这使得 HAND 缺乏有效的治疗方法。HIV 蛋白转录激活因子(Tat)作为一种重要的调节蛋白,在手 HAND 的发病机制中起着关键作用,其 HAND 机制受到广泛关注。血脑屏障(BBB)及其细胞成分脑微血管内皮细胞(BMVECs)在保护中枢神经系统(CNS)方面发挥着必要的作用,其与 Tat 相关的损伤是 HAND 的潜在治疗靶点。在这篇综述中,我们将研究 Tat 介导的 BBB 损伤机制,并提供与 Tat 引起的 BMVEC 损伤相关的多种证据。

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Front Immunol. 2025-8-7

[2]
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[3]
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Int J Mol Sci. 2025-7-13

[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
HIV-1 Tat induced microglial EVs leads to neuronal synaptodendritic injury: microglia-neuron cross-talk in NeuroHIV.

Extracell Vesicles Circ Nucl Acids. 2022

[2]
The potential role of HIV-1 latency in promoting neuroinflammation and HIV-1-associated neurocognitive disorder.

Trends Immunol. 2022-8

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HIV Promotes Neurocognitive Impairment by Damaging the Hippocampal Microvessels.

Mol Neurobiol. 2022-8

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HIV-Associated Neurotoxicity: The Interplay of Host and Viral Proteins.

Mediators Inflamm. 2021

[5]
Ca homeostasis in brain microvascular endothelial cells.

Int Rev Cell Mol Biol. 2021

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Disruption of the blood-brain barrier in 22q11.2 deletion syndrome.

Brain. 2021-6-22

[7]
Methamphetamine and HIV-Tat Protein Synergistically Induce Oxidative Stress and Blood-Brain Barrier Damage via Transient Receptor Potential Melastatin 2 Channel.

Front Pharmacol. 2021-3-17

[8]
Latent HIV-Exosomes Induce Mitochondrial Hyperfusion Due to Loss of Phosphorylated Dynamin-Related Protein 1 in Brain Endothelium.

Mol Neurobiol. 2021-6

[9]
Rho-kinase inhibitor hydroxyfasudil protects against HIV-1 Tat-induced dysfunction of tight junction and neprilysin/Aβ transfer receptor expression in mouse brain microvessels.

Mol Cell Biochem. 2021-5

[10]
HIV TAT-mediated microglial senescence: Role of SIRT3-dependent mitochondrial oxidative stress.

Redox Biol. 2021-4

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