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A Zebrafish Live Imaging Model Reveals Differential Responses of Microglia Toward Glioblastoma Cells In Vivo

机译:斑马鱼的实时成像模型揭示了小胶质细胞对胶质母细胞瘤细胞的体内差异反应。

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摘要

Glioblastoma multiforme is the most common and deadliest form of brain cancer. Glioblastomas are infiltrated by a high number of microglia, which promote tumor growth and surrounding tissue invasion. However, it is unclear how microglia and glioma cells physically interact and if there are differences, depending on glioma cell type. Hence, we have developed a novel live imaging assay to study microglia–glioma interactions in vivo in the zebrafish brain. We transplanted well-established human glioblastoma cell lines, U87 and U251, into transgenic zebrafish lines with labelled macrophages/microglia. Our confocal live imaging results show distinct interactions between microglia and U87, as well as U251 glioblastoma cells that differ in number and nature. Importantly these interactions do not appear to be antitumoral as zebrafish microglia do not engulf and phagocytose the human glioblastoma cells. Finally, xenotransplants into the irf8−/− zebrafish mutant that lacks microglia, as well as pharmacological inhibition of the CSF-1 receptor (CSF-1R) on microglia, confirm a prominent role for zebrafish microglia in promoting human glioblastoma cell growth. This new model will be an important tool for drug screening and the development of future immunotherapeutics targeting microglia within glioma.
机译:胶质母细胞瘤是最常见和最致命的脑癌形式。大量的小胶质细胞浸润了胶质母细胞瘤,这促进了肿瘤的生长和周围组织的侵袭。然而,取决于神经胶质瘤细胞类型,尚不清楚小胶质细胞和神经胶质瘤细胞如何物理相互作用以及是否存在差异。因此,我们开发了一种新颖的实时成像测定法,以研究斑马鱼脑中体内的小胶质细胞-神经胶质瘤相互作用。我们将成熟的人类胶质母细胞瘤细胞系U87和U251移植到带有标记巨噬细胞/小胶质细胞的转基因斑马鱼系中。我们的共聚焦实时成像结果显示,小胶质细胞与U87以及数量和性质不同的U251胶质母细胞瘤细胞之间存在明显的相互作用。重要的是,这些相互作用似乎没有抗肿瘤作用,因为斑马鱼小胶质细胞没有吞噬和吞噬人类胶质母细胞瘤细胞。最后,异种移植到缺少小胶质细胞的irf8 -/-斑马鱼突变体中,以及对小胶质细胞的CSF-1受体(CSF-1R)的药理抑制作用,证实了斑马鱼小胶质细胞在促进人胶质母细胞瘤细胞生长。这一新模型将成为药物筛选和针对神经胶质瘤内小胶质细胞的未来免疫疗法发展的重要工具。

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