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In vivo imaging of activated microglia in a mouse model of focal cerebral ischemia by two-photon microscopy

机译:双光子显微镜在小鼠局灶性脑缺血模型中激活小胶质细胞的体内成像

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摘要

Microglia are brain resident macrophages rapidly responding to various stimuli to exert appropriate inflammatory responses. Although they have recently been exploited as an attractive candidate for imaging neuroinflammation, it is still difficult to visualize them at the cellular and molecular levels. Here we imaged activated microglia by establishing intracranial window chamber (ICW) in a mouse model of focal cerebral ischemia by using two-photon microscopy (TPM), in vivo. Intravenous injection of fluorescent antibodies allowed us to detect significantly elevated levels of Iba-1 and CD68 positive activated microglia in the ipsilateral compared to the contralateral side of the infarct. We further observed that indomethacin, a non-steroidal anti-inflammatory drug significantly attenuated CD68-positive microglial activation in ICW, which was further confirmed by qRT-PCR biochemical analyses. In conclusion, we believe that in vivo TPM imaging of ICW would be a useful tool to screen for therapeutic interventions lowering microglial activation hence neuroinflammation.
机译:小胶质细胞是常驻在大脑的巨噬细胞,对各种刺激反应迅速,以施加适当的炎症反应。尽管最近已将它们开发为用于成像神经炎症的诱人候选物,但仍然很难在细胞和分子水平上对其进行可视化。在这里,我们通过在体内使用双光子显微镜(TPM)在局灶性脑缺血的小鼠模型中建立颅内窗小室(ICW)来成像激活的小胶质细胞。与梗塞的对侧相比,静脉注射荧光抗体使我们能够检测到同侧Iba-1和CD68阳性活化小胶质细胞的水平显着升高。我们进一步观察到消炎痛是一种非甾体类抗炎药,可显着减弱ICW中CD68阳性的小胶质细胞活化,这已通过qRT-PCR生化分析进一步证实。总之,我们认为,ICW的体内TPM成像将是筛选降低小胶质细胞活化从而降低神经炎症的治疗干预措施的有用工具。

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