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激活的小胶质细胞破坏血脑屏障并在大鼠模型中诱导趋化因子和细胞因子

Activated Microglia Disrupt the Blood-Brain Barrier and Induce Chemokines and Cytokines in a Rat Model.

作者信息

Shigemoto-Mogami Yukari, Hoshikawa Kazue, Sato Kaoru

机构信息

Laboratory of Neuropharmacology, Division of Pharmacology, National Institute of Health Sciences, Kawasaki-ku, Japan.

Department of Neuropharmacology, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.

出版信息

Front Cell Neurosci. 2018 Dec 13;12:494. doi: 10.3389/fncel.2018.00494. eCollection 2018.

Abstract

Severe neuroinflammation is associated with blood brain barrier (BBB) disruption in CNS diseases. Although microglial activation and the subsequent changes in cytokine/chemokine (C/C) concentrations are thought to be key steps in the development of neuroinflammation, little data are available concerning the interaction of microglia with BBB cells. In this study, we investigated this interaction by adding LPS-activated microglia (LPS-MG) to the abluminal side of a BBB model composed of endothelial cells (EC), pericytes (Peri) and astrocytes (Ast). We then examined the abluminal concentrations of 27 C/Cs and the interactions between the LPS-MG and BBB cells. LPS-MG caused collapse of the BBB, revealed by decreases in the trans-endothelial electrical resistance (TEER) and by changes in the expression levels of tight junction (TJ) proteins. Under these conditions, 19 C/Cs were markedly increased on the abluminal side. Unexpectedly, although LPS-MG alone released 10 of the 19 C/Cs, their concentrations were much lower than those detected on the abluminal side of the BBB model supplemented with LPS-MG. Co-culture of LPS-MG with Ast caused marked increases in 12 of the 19 C/Cs, while co-culture of LPS-MG with EC and Peri resulted in a significant increase in only 1 of the 19 C/Cs (fractalkine). These results suggest that C/C dynamics in this system are not only caused by activated microglia but also are due to the interaction between activated microglia and astrocytes.

摘要

在中枢神经系统疾病中,严重的神经炎症与血脑屏障(BBB)破坏有关。尽管小胶质细胞激活以及随后细胞因子/趋化因子(C/C)浓度的变化被认为是神经炎症发展的关键步骤,但关于小胶质细胞与血脑屏障细胞相互作用的数据却很少。在本研究中,我们通过将脂多糖激活的小胶质细胞(LPS-MG)添加到由内皮细胞(EC)、周细胞(Peri)和星形胶质细胞(Ast)组成的血脑屏障模型的管腔外侧,来研究这种相互作用。然后,我们检测了27种C/Cs的管腔外侧浓度以及LPS-MG与血脑屏障细胞之间的相互作用。LPS-MG导致血脑屏障崩溃,这通过跨内皮电阻(TEER)降低和紧密连接(TJ)蛋白表达水平的变化得以体现。在这些条件下,19种C/Cs在管腔外侧显著增加。出乎意料的是,尽管单独的LPS-MG释放了19种C/Cs中的10种,但其浓度远低于在添加了LPS-MG的血脑屏障模型管腔外侧检测到的浓度。LPS-MG与Ast共培养导致19种C/Cs中的12种显著增加,而LPS-MG与EC和Peri共培养仅使19种C/Cs中的1种( fractalkine)显著增加。这些结果表明,该系统中的C/C动态变化不仅由活化的小胶质细胞引起,还归因于活化的小胶质细胞与星形胶质细胞之间的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e33b/6300509/64a5f602111a/fncel-12-00494-g0001.jpg

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