Department of Pathology &, Laboratory Medicine Lewis Katz School of Medicine at Temple University, 3500 N Broad St, PA, 19140, Philadelphia, USA.
The Center for Substance Abuse Research Lewis Katz School of Medicine at Temple University, 3500 N Broad St, PA, 19140, Philadelphia, USA.
J Neuroimmune Pharmacol. 2021 Dec;16(4):785-795. doi: 10.1007/s11481-021-10008-5. Epub 2021 Aug 26.
Treatment of HIV-infected patients with antiretroviral therapy (ART) has effectively suppressed viral replication; however, the central nervous system is still a major target and reservoir of the virus leading to the possible development of HIV-associated neurocognitive disorders (HAND). Furthermore, a hallmark feature of HAND is the disruption of the blood-brain barrier that leads to loss of tight junction protein (TJP) complexes. Extracellular vesicles (EVs), released by every cell type in the body, occur in greater quantities in response to cellular activation or injury. We have found that inflammatory insults activate brain endothelial cells (EC) and induce the release of EVs containing TJPs such as Occludin. We thus hypothesized that HIV infection and unresolved neuroinflammation will result in the release of brain-EC derived EVs. Herein, our results show elevated levels of brain-EC EVs in a humanized mouse model of HIV infection. Furthermore, while ART reduced brain-EC EVs, it was unable to completely resolve increased vesicles detectable in the blood. In addition to inflammatory insults, HIV-1 viral proteins (Tat and gp120) increased the release of Occludin + vesicles from human brain microvasculature ECs. This increase in vesicle release could be prevented by knock-down of the small GTPase ARF6. ARF6 has been shown to regulate EV biogenesis in other cell types, and we provide further evidence for the involvement of ARF6 in brain EC derived EVs. Overall, this study offers insight into the process of brain vascular remodeling (via EVs) in the setting of neuroinflammation and thus provides possibilities for biomarker monitoring and targeting of ARF6.
抗逆转录病毒疗法 (ART) 治疗感染 HIV 的患者已有效抑制病毒复制;然而,中枢神经系统仍然是病毒的主要靶点和储存库,导致可能发生与 HIV 相关的神经认知障碍 (HAND)。此外,HAND 的一个标志特征是血脑屏障的破坏,导致紧密连接蛋白 (TJP) 复合物的丧失。细胞外囊泡 (EV) 是由体内每种细胞类型释放的,在细胞激活或损伤时会以更大的量释放。我们发现,炎症损伤激活脑内皮细胞 (EC),并诱导释放含有 Occludin 等 TJPs 的 EV。因此,我们假设 HIV 感染和未解决的神经炎症会导致脑 EC 衍生的 EV 释放。在此,我们的研究结果显示,HIV 感染的人类化小鼠模型中脑 EC 衍生的 EV 水平升高。此外,尽管 ART 降低了脑 EC EVs 的水平,但仍无法完全消除血液中可检测到的增加的囊泡。除了炎症损伤外,HIV-1 病毒蛋白 (Tat 和 gp120) 增加了人脑微血管内皮细胞 Occludin + 囊泡的释放。通过 ARF6 的小 GTPase 敲低可以防止囊泡释放增加。ARF6 已被证明可调节其他细胞类型中 EV 的生物发生,我们为 ARF6 参与脑 EC 衍生的 EV 提供了进一步的证据。总的来说,这项研究深入了解了神经炎症背景下脑血管重塑 (通过 EVs) 的过程,从而为 ARF6 的生物标志物监测和靶向提供了可能性。