开发三维脑模型以研究出血性中风后的性别特异性神经炎症

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Translational Stroke Research Pub Date : 2025-06-01 Epub Date: 2024-04-01 DOI:10.1007/s12975-024-01243-y
Rezwanul Islam, Hadi Hasan Choudhary, Hritik Mehta, Feng Zhang, Tudor G Jovin, Khalid A Hanafy
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引用次数: 0

摘要

蛛网膜下腔出血(SAH)占中风的 5%,与男性相比,女性的炎症反应较弱;但这一机制尚未确定。蛛网膜下腔出血研究的一个障碍是缺乏人脑模型。小鼠模型的研究很有帮助,但人类模型应结合使用,以提高可转化性。这些观察结果促使我们开发了一种三维系统,以研究新型体外人类 SAH 模型中的性别特异性小胶质细胞和神经胶质细胞功能,并将其与我们已验证的体内 SAH 模型进行比较。我们的实验室开发了一种基于膜的三维体外细胞培养系统,其中包括人类星形胶质细胞、小胶质细胞和神经元。三维培养物与来自神经重症监护室(Neuro-ICU)SAH 患者的男性和女性脑脊液一起培养。此外,还研究了小胶质细胞的形态、红细胞吞噬功能、小胶质细胞炎症细胞因子的产生和神经元凋亡,并与我们的小鼠 SAH 模型进行了比较。人类三维系统显示了与成人大脑相似的细胞间相互作用和三种细胞类型的比例。通过形态学和流式细胞术,SAH 的体外和体内模型显示雄性小胶质细胞比雌性小胶质细胞更具炎症性。相反,体外和体内模型都显示,雌性小胶质细胞比雄性小胶质细胞更具吞噬能力,更不容易损伤神经元。雌性小胶质细胞吞噬能力增强的一个可能原因是 CD206 和 MerTK 的表达量增加。我们的体外人类三维细胞培养 SAH 模型与体内小鼠 SAH 模型在小胶质细胞形态、炎症和吞噬能力方面的性别比较结果相似。SAH的人类三维脑模型可能是小鼠模型的有用辅助工具,能更好地应用于SAH患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a 3D Brain Model to Study Sex-Specific Neuroinflammation After Hemorrhagic Stroke.

Subarachnoid hemorrhage (SAH) accounts for 5% of stroke, with women having a decreased inflammatory response compared to men; however, this mechanism has yet to be identified. One hurdle in SAH research is the lack of human brain models. Studies in murine models are helpful, but human models should be used in conjunction for improved translatability. These observations lead us to develop a 3D system to study the sex-specific microglial and neuroglial function in a novel in vitro human SAH model and compare it to our validated in vivo SAH model. Our lab has developed a 3D, membrane-based in vitro cell culture system with human astrocytes, microglia, and neurons from both sexes. The 3D cultures were incubated with male and female cerebrospinal fluid from SAH patients in the Neuro-ICU. Furthermore, microglial morphology, erythrophagocytosis, microglial inflammatory cytokine production, and neuronal apoptosis were studied and compared with our murine SAH models. The human 3D system demonstrated intercellular interactions and proportions of the three cell types similar to the adult human brain. In vitro and in vivo models of SAH showed concordance in male microglia being more inflammatory than females via morphology and flow cytometry. On the contrary, both in vitro and in vivo models revealed that female microglia were more phagocytic and less prone to damaging neurons than males. One possible explanation for the increased phagocytic ability of female microglia was the increased expression of CD206 and MerTK. Our in vitro, human, 3D cell culture SAH model showed similar results to our in vivo murine SAH model with respect to microglial morphology, inflammation, and phagocytosis when comparing the sexes. A human 3D brain model of SAH may be a useful adjunct to murine models to improve translation to SAH patients.

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来源期刊
Translational Stroke Research
Translational Stroke Research CLINICAL NEUROLOGY-NEUROSCIENCES
CiteScore
13.80
自引率
4.30%
发文量
130
审稿时长
6-12 weeks
期刊介绍: Translational Stroke Research covers basic, translational, and clinical studies. The Journal emphasizes novel approaches to help both to understand clinical phenomenon through basic science tools, and to translate basic science discoveries into the development of new strategies for the prevention, assessment, treatment, and enhancement of central nervous system repair after stroke and other forms of neurotrauma. Translational Stroke Research focuses on translational research and is relevant to both basic scientists and physicians, including but not restricted to neuroscientists, vascular biologists, neurologists, neuroimagers, and neurosurgeons.
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