用于评估创伤性脑损伤反应的三维神经血管单元组织模型

Liam Power, Rita Shuhmaher, Philip Houtz, Jinpeng Chen, Sara Rudolph, John Yuen, Majd Machour, Emily Levy, Limin Wu, Shulamit Levenberg, Michael Whalen, Ying Chen, David L Kaplan
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引用次数: 0

摘要

神经血管单元(NVU)是中枢神经系统中的一个关键界面,它将血管与神经胶质细胞和神经组织的相互作用联系在一起。神经血管单元的破坏与神经退行性疾病的发生和发展有关。尽管 NVU 非常重要,但以生理相关的方式对其进行研究仍具有挑战性。在这里,我们开发了一种 NVU 的三维细胞培养模型,它将人类原代脑微血管内皮细胞、星形胶质细胞和周细胞纳入一个可在体外维持数周的组织系统中。这种组织模型有助于再现 NVU 的复杂性,可用于研究疾病和细胞间相互作用的机制。NVU 组织模型在机械损伤后显示出细胞死亡和炎症反应升高,以模拟受控实验室条件下的创伤性脑损伤(TBI),包括乳酸脱氢酶(LDH)释放、炎症标志物 TNF-α 和单核细胞趋化细胞因子 MCP-2 和 MCP-3 升高以及紧密连接标志物 ZO-1 表达降低。这种三维组织模型可作为一种工具,用于破译创伤性脑损伤的机理以及与 NVU 相关的免疫反应。
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3D Neurovascular Unit Tissue Model to Assess Responses to Traumatic Brain Injury.

The neurovascular unit (NVU) is a critical interface in the central nervous system that links vascular interactions with glial and neural tissue. Disruption of the NVU has been linked to the onset and progression of neurodegenerative diseases. Despite its significance the NVU remains challenging to study in a physiologically relevant manner. Here, a 3D cell triculture model of the NVU is developed that incorporates human primary brain microvascular endothelial cells, astrocytes, and pericytes into a tissue system that can be sustained in vitro for several weeks. This tissue model helps recapitulate the complexity of the NVU and can be used to interrogate the mechanisms of disease and cell-cell interactions. The NVU tissue model displays elevated cell death and inflammatory responses following mechanical damage, to emulate traumatic brain injury (TBI) under controlled laboratory conditions, including lactate dehydrogenase (LDH) release, elevated inflammatory markers TNF-α and monocyte chemoattractant cytokines MCP-2 and MCP-3 and reduced expression of the tight junction marker ZO-1. This 3D tissue model serves as a tool for deciphering mechanisms of TBIs and immune responses associated with the NVU.

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