Daijin Li, Jie Chang, Yujue Wang, Xiaoye Du, Jing Xu, Jingang Cui, Teng Zhang, Yu Chen
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Upon verifying the anti-inflammatory effects of hyperoside in LPS-stimulated BV-2 cells, our results here further demonstrated that post-light damage hyperoside treatment mitigated the loss of photoreceptors and attenuated the functional decline of the retina. Meanwhile, post-light damage hyperoside treatment lowered neuroinflammatory responses and dampened microglial activation in the illuminated retinas. With respect to microglial activation, hyperoside mitigated the pro-inflammatory responses in DNA-stimulated BV-2 cells and lowered DNA-stimulated production of 2'3'-cGAMP in BV-2 cells. Moreover, hyperoside was shown to directly interact with cGAS and suppress the enzymatic activity of cGAS in a cell-free system. In conclusion, the current study suggests for the first time that the DNA sensor cGAS is a direct target of hyperoside. 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引用次数: 0
摘要
活化的小胶质细胞在驱动视网膜中与光感受器变性相关的神经炎症方面发挥着重要作用。控制小胶质细胞的促炎激活有望缓解感光器变性的进展。金丝桃苷是一种天然黄酮醇苷,具有抗氧化和抗炎活性,我们之前的研究表明,在光损伤前处理金丝桃苷可以防止光氧化应激诱导的视网膜感光器变性和神经炎症反应。然而,金丝桃苷对光感受器退化过程中小胶质细胞介导的神经炎症的直接影响仍然未知。在验证了金丝桃苷对 LPS 刺激的 BV-2 细胞的抗炎作用后,我们的研究结果进一步证明,光损伤后的金丝桃苷处理可减轻光感受器的损失,并减轻视网膜功能的衰退。同时,光损伤后的金丝桃苷处理降低了神经炎症反应,抑制了照明视网膜中的小胶质细胞活化。在小胶质细胞活化方面,金丝桃苷减轻了 DNA 刺激的 BV-2 细胞的促炎反应,并降低了 DNA 刺激的 BV-2 细胞中 2'3'-cGAMP 的产生。此外,在无细胞系统中,金丝桃苷还能与 cGAS 直接相互作用,抑制 cGAS 的酶活性。总之,目前的研究首次表明,DNA 传感器 cGAS 是金丝桃苷的直接靶标。金丝桃苷能有效减轻 DNA 刺激 cGAS 介导的小胶质细胞促炎激活,这可能有助于金丝桃苷在抑制神经炎症和减轻神经炎症诱发的感光细胞变性方面的治疗效果。
Hyperoside mitigates photoreceptor degeneration in part by targeting cGAS and suppressing DNA-induced microglial activation.
Activated microglia play an important role in driving photoreceptor degeneration-associated neuroinflammation in the retina. Controlling pro-inflammatory activation of microglia holds promise for mitigating the progression of photoreceptor degeneration. Our previous study has demonstrated that pre-light damage treatment of hyperoside, a naturally occurring flavonol glycoside with antioxidant and anti-inflammatory activities, prevents photooxidative stress-induced photoreceptor degeneration and neuroinflammatory responses in the retina. However, the direct impact of hyperoside on microglia-mediated neuroinflammation during photoreceptor degeneration remains unknown. Upon verifying the anti-inflammatory effects of hyperoside in LPS-stimulated BV-2 cells, our results here further demonstrated that post-light damage hyperoside treatment mitigated the loss of photoreceptors and attenuated the functional decline of the retina. Meanwhile, post-light damage hyperoside treatment lowered neuroinflammatory responses and dampened microglial activation in the illuminated retinas. With respect to microglial activation, hyperoside mitigated the pro-inflammatory responses in DNA-stimulated BV-2 cells and lowered DNA-stimulated production of 2'3'-cGAMP in BV-2 cells. Moreover, hyperoside was shown to directly interact with cGAS and suppress the enzymatic activity of cGAS in a cell-free system. In conclusion, the current study suggests for the first time that the DNA sensor cGAS is a direct target of hyperoside. Hyperoside is effective at mitigating DNA-stimulated cGAS-mediated pro-inflammatory activation of microglia, which likely contributes to the therapeutic effects of hyperoside at curtailing neuroinflammation and alleviating neuroinflammation-instigated photoreceptor degeneration.
期刊介绍:
"Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders.
ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.