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首页> 外文期刊>Cell death & disease. >Inhibition of AIM2 inflammasome activation alleviates GSDMD-induced pyroptosis in early brain injury after subarachnoid haemorrhage
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Inhibition of AIM2 inflammasome activation alleviates GSDMD-induced pyroptosis in early brain injury after subarachnoid haemorrhage

机译:抑制AIM2炎症激活减轻了蛛网膜下腔出血后早期脑损伤的GSDMD诱导的γ损伤

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摘要

Only a few types of inflammasomes have been described in central nervous system cells. Among these, the absent in melanoma 2 (AIM2) inflammasome is primarily found in neurons, is highly specific and can be activated only by double-stranded DNA. Although it has been demonstrated that the AIM2 inflammasome is activated by poly(deoxyadenylic-deoxythymidylic) acid sodium salt and leads to pyroptotic neuronal cell death, the role of AIM2 inflammasome-mediated pyroptosis in early brain injury (EBI) after subarachnoid haemorrhage (SAH) has rarely been studied. Thus, we designed this study to explore the mechanism of gasdermin D(GSDMD)-induced pyroptosis mediated by the AIM2 inflammasome in EBI after SAH. The level of AIM2 from the cerebrospinal fluid (CSF) of patients with SAH was detected. The pathway of AIM2 inflammasome-mediated pyroptosis, the AIM2/Caspase-1/GSDMD pathway, was explored after experimental SAH in vivo and in primary cortical neurons stimulated by oxyhaemoglobin (oxyHb) in vitro. Then, we evaluated GSDMD-induced pyroptosis mediated by the AIM2 inflammasome in AIM2 and caspase-1- deficient mice and primary cortical neurons generated through lentivirus (LV) knockdown. Compared with that of the control samples, the AIM2 level in the CSF of the patients with SAH was significantly increased. Pyroptosis-associated proteins mediated by the AIM2 inflammasome were significantly increased in vivo and in vitro following experimentally induced SAH. After AIM2 and caspase-1 were knocked down by an LV, GSDMD-induced pyroptosis mediated by the AIM2 inflammasome was alleviated in EBI after SAH. Intriguingly, when caspase-1 was knocked down, apoptosis was significantly suppressed via impeding the activation of caspase-3. GSDMD-induced pyroptosis mediated by the AIM2 inflammasome may be involved in EBI following SAH. The inhibition of AIM2 inflammasome activation caused by knocking down AIM2 and caspase-1 alleviates GSDMD-induced pyroptosis in EBI after SAH.
机译:中枢神经系统细胞中仅描述了几种类型的炎性血症。其中,黑色素瘤2(AIM2)炎症中的缺席主要在神经元中发现,高度特异性,并且可以仅通过双链DNA激活。虽然已经证明了Aim2炎性炎症由聚(脱氧酰基 - 脱氧)酸钠盐激活,并导致糊状不异的神经元细胞死亡,Aim2炎炎症介导的糊化症在蛛网膜下腔出血后早期脑损伤(EBI)的作用(SAH)很少研究过。因此,我们设计了该研究,探讨了在SAH之后EBI的Aim2炎症介导的胃蛋白D(GSDMD)诱导的糊酶的机制。检测到SAH患者脑脊髓液(CSF)的AIM2水平。 AIM2炎症介导的辐射虫,AIM2 / Caspase-1 / GSDMD途径的途径在体内和体外刺激的氧血红蛋白(氧气氧化氢脲刺激的原发性皮质神经元后,探讨了AIM2 / Caspase-1 / GSDMD途径。然后,我们评估了通过慢病毒(LV)敲低产生的Aim2和Caspase-1-缺陷小鼠和初级皮质神经元的Aim2炎症介导的GSDMD诱导的胃泌素。与对照样品相比,SAH患者CSF中的AIM2水平显着增加。在实验诱导的SAH中,体内和体内炎症的催化剂相关蛋白质显着增加。 Aim2和Caspase-1通过LV撞击后,在SAH后,通过AIM2炎性炎炎症介导的GSDMD诱导的辐射瘤菌被缓解在EBI中。有趣的是,当Caspase-1被敲下来时,通过阻碍Caspase-3的活化,显着抑制细胞凋亡。 GSDMD诱导的诱导的Aim2炎性炎症瘤病可能参与eBi之后SAH。抑制Aim2炎症激活因爆震而导致的Aim2和Caspase-1缓解了SAH后EBI的GSDMD诱导的γ凋亡。

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