NLRP3 promotes radiation-induced brain injury by regulating microglial pyroptosis.

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
Wan Zhang, Qiheng Wu, Xiaonan Zhang, Yue Qin, Lianxuan Gao, Shushu Hu, Shasha Du, Chen Ren
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Abstract

Purpose: Radiation-induced brain injury, one of the side effects of cranial radiotherapy in tumour patients, usually results in durable and serious cognitive disorders. Microglia are important innate immune-effector cells in the central nervous system. However, the interaction between microglia and neurons in radiation-induced brain injury remains uncharacterised.

Methods and materials: We established a microglia-neuron indirect co-culture model to assess the interaction between them. Microglia exposed to radiation were examined for pyroptosis using lactate dehydrogenase (LDH) release, Annexin V/PI staining, SYTOX staining and western blot. The role of nucleotide-binding oligomerisation domain-like receptor family pyrin domain containing 3 (NLRP3) was investigated in microglia exposed to radiation and in mouse radiation brain injury model through siRNA or inhibitor. Mini-mental state examination and cytokines in blood were performed in 23 patients who had experienced cranial irradiation.

Results: Microglia exerted neurotoxic features after radiation in the co-culture model. NLRP3 was up-regulated in microglia exposed to radiation, and then caspase-1 was activated. Thus, the gasdermin D protein was cleaved, and it triggered pyroptosis in microglia, which released inflammatory cytokines. Meanwhile, treatment with siRNA NLRP3 in vitro and NLRP3 inhibitor in vivo attenuated the damaged neuron cell and cognitive impairment, respectively. What is more, we found that the patients after radiation with higher IL-6 were observed to have a decreased MMSE score.

Conclusions: These findings indicate that radiation-induced pyroptosis in microglia may promote radiation-induced brain injury via the secretion of neurotoxic cytokines. NLRP3 was evaluated as an important mediator in radiation-induced pyroptosis and a promising therapeutic target for radiation-induced brain injury.

NLRP3通过调节小胶质细胞的热解促进辐射诱导的脑损伤。
目的:放射诱导的脑损伤是肿瘤患者颅脑放疗的副作用之一,通常会导致持久和严重的认知障碍。小胶质细胞是中枢神经系统中重要的先天性免疫效应细胞。然而,小胶质细胞与神经元之间在辐射诱导的脑损伤中的相互作用仍未定性:我们建立了一个小胶质细胞-神经元间接共培养模型来评估它们之间的相互作用。通过乳酸脱氢酶(LDH)释放、Annexin V/PI染色、SYTOX染色和Western blot检测暴露于辐射的小胶质细胞的热凋亡。通过 siRNA 或抑制剂,研究了核苷酸结合寡聚化域样受体家族含吡啶域 3(NLRP3)在暴露于辐射的小胶质细胞和小鼠辐射性脑损伤模型中的作用。对 23 名接受过颅脑照射的患者进行了迷你精神状态检查和血液细胞因子检测:结果:在共培养模型中,辐射后小胶质细胞具有神经毒性特征。结果:在共培养模型中,辐射后的小胶质细胞具有神经毒性特征,NLRP3 在小胶质细胞中上调,然后 caspase-1 被激活。因此,gasdermin D 蛋白被裂解,并引发小胶质细胞的热凋亡,释放出炎性细胞因子。同时,体外 siRNA NLRP3 和体内 NLRP3 抑制剂分别减轻了受损神经元细胞和认知障碍。此外,我们还发现,IL-6较高的辐射后患者的MMSE评分下降:这些研究结果表明,辐射诱导的小胶质细胞热解可能会通过分泌神经毒性细胞因子促进辐射诱导的脑损伤。NLRP3被评估为辐射诱导的脓毒症的一个重要介质,也是治疗辐射诱导的脑损伤的一个有希望的靶点。
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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
87
审稿时长
6-12 weeks
期刊介绍: Neuropathology and Applied Neurobiology is an international journal for the publication of original papers, both clinical and experimental, on problems and pathological processes in neuropathology and muscle disease. Established in 1974, this reputable and well respected journal is an international journal sponsored by the British Neuropathological Society, one of the world leading societies for Neuropathology, pioneering research and scientific endeavour with a global membership base. Additionally members of the British Neuropathological Society get 50% off the cost of print colour on acceptance of their article.
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