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打开创伤性脑损伤的黑匣子:一种结合人类三维神经组织和创伤性脑损伤诱导装置的整体方法。

Opening the black box of traumatic brain injury: a holistic approach combining human 3D neural tissue and an traumatic brain injury induction device.

作者信息

Loussert-Fonta Céline, Stoppini Luc, Neuenschwander Yoan, Righini Ophélie, Prim Denis, Schmidt Cédric, Heuschkel Marc O, Gomez Baisac Loris, Jovic Milica, Pfeifer Marc E, Extermann Jérôme, Roux Adrien

机构信息

Tissue Engineering Laboratory, HEPIA HES-SO University of Applied Sciences and Arts Western Switzerland, Geneva, Switzerland.

Micro-Nanotechnology Group, HEPIA HES-SO University of Applied Sciences and Arts Western Switzerland, Geneva, Switzerland.

出版信息

Front Neurosci. 2023 Jun 15;17:1189615. doi: 10.3389/fnins.2023.1189615. eCollection 2023.

Abstract

Traumatic brain injury (TBI) is caused by a wide range of physical events and can induce an even larger spectrum of short- to long-term pathophysiologies. Neuroscientists have relied on animal models to understand the relationship between mechanical damages and functional alterations of neural cells. These and animal-based models represent important approaches to mimic traumas on whole brains or organized brain structures but are not fully representative of pathologies occurring after traumas on human brain parenchyma. To overcome these limitations and to establish a more accurate and comprehensive model of human TBI, we engineered an platform to induce injuries via the controlled projection of a small drop of liquid onto a 3D neural tissue engineered from human iPS cells. With this platform, biological mechanisms involved in neural cellular injury are recorded through electrophysiology measurements, quantification of biomarkers released, and two imaging methods [confocal laser scanning microscope (CLSM) and optical projection tomography (OPT)]. The results showed drastic changes in tissue electrophysiological activities and significant releases of glial and neuronal biomarkers. Tissue imaging allowed us to reconstruct the injured area spatially in 3D after staining it with specific nuclear dyes and to determine TBI resulting in cell death. In future experiments, we seek to monitor the effects of TBI-induced injuries over a prolonged time and at a higher temporal resolution to better understand the subtleties of the biomarker release kinetics and the cell recovery phases.

摘要

创伤性脑损伤(TBI)由多种物理事件引起,可诱发从短期到长期的更大范围的病理生理变化。神经科学家依靠动物模型来理解神经细胞的机械损伤与功能改变之间的关系。这些基于动物的模型是模拟全脑或有组织的脑结构创伤的重要方法,但并不完全代表人类脑实质创伤后发生的病理情况。为了克服这些局限性并建立更准确、更全面的人类TBI模型,我们设计了一个平台,通过将一小滴液体可控地投射到由人类诱导多能干细胞工程化构建的3D神经组织上来诱导损伤。利用这个平台,通过电生理测量、释放的生物标志物定量以及两种成像方法[共聚焦激光扫描显微镜(CLSM)和光学投影断层扫描(OPT)]来记录神经细胞损伤所涉及的生物学机制。结果显示组织电生理活动发生了剧烈变化,神经胶质和神经元生物标志物大量释放。组织成像使我们能够在用特定核染料染色后在三维空间中重建损伤区域,并确定导致细胞死亡的TBI情况。在未来的实验中,我们试图在更长时间内以更高的时间分辨率监测TBI诱导损伤的影响,以更好地理解生物标志物释放动力学和细胞恢复阶段的细微之处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ca/10308006/6d9a663730fa/fnins-17-1189615-g0001.jpg

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