Overexpression of low-density lipoprotein receptor prevents neurotoxic polarization of astrocytes via inhibiting NLRP3 inflammasome activation in experimental ischemic stroke.

IF 5.9 2区 医学 Q2 CELL BIOLOGY
Neural Regeneration Research Pub Date : 2025-02-01 Epub Date: 2024-04-16 DOI:10.4103/NRR.NRR-D-23-01263
Shuai Feng, Juanji Li, Tingting Liu, Shiqi Huang, Xiangliang Chen, Shen Liu, Junshan Zhou, Hongdong Zhao, Ye Hong
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引用次数: 0

Abstract

JOURNAL/nrgr/04.03/01300535-202502000-00027/figure1/v/2024-05-28T214302Z/r/image-tiff Neurotoxic astrocytes are a promising therapeutic target for the attenuation of cerebral ischemia/reperfusion injury. Low-density lipoprotein receptor, a classic cholesterol regulatory receptor, has been found to inhibit NLR family pyrin domain containing protein 3 (NLRP3) inflammasome activation in neurons following ischemic stroke and to suppress the activation of microglia and astrocytes in individuals with Alzheimer's disease. However, little is known about the effects of low-density lipoprotein receptor on astrocytic activation in ischemic stroke. To address this issue in the present study, we examined the mechanisms by which low-density lipoprotein receptor regulates astrocytic polarization in ischemic stroke models. First, we examined low-density lipoprotein receptor expression in astrocytes via immunofluorescence staining and western blotting analysis. We observed significant downregulation of low-density lipoprotein receptor following middle cerebral artery occlusion reperfusion and oxygen-glucose deprivation/reoxygenation. Second, we induced the astrocyte-specific overexpression of low-density lipoprotein receptor using astrocyte-specific adeno-associated virus. Low-density lipoprotein receptor overexpression in astrocytes improved neurological outcomes in middle cerebral artery occlusion mice and reversed neurotoxic astrocytes to create a neuroprotective phenotype. Finally, we found that the overexpression of low-density lipoprotein receptor inhibited NLRP3 inflammasome activation in oxygen-glucose deprivation/reoxygenation injured astrocytes and that the addition of nigericin, an NLRP3 agonist, restored the neurotoxic astrocyte phenotype. These findings suggest that low-density lipoprotein receptor could inhibit the NLRP3-meidiated neurotoxic polarization of astrocytes and that increasing low-density lipoprotein receptor in astrocytes might represent a novel strategy for treating cerebral ischemic stroke.

在实验性缺血性脑卒中中,过表达低密度脂蛋白受体可通过抑制 NLRP3 炎症小体的激活防止星形胶质细胞的神经毒性极化。
JOURNAL/nrgr/04.03/01300535-202502000-00027/figure1/v/2024-05-28T214302Z/r/image-tiff 神经毒性星形胶质细胞是减轻脑缺血再灌注损伤的一个很有前景的治疗靶点。低密度脂蛋白受体是一种典型的胆固醇调节受体,研究发现它能抑制缺血性中风后神经元中的 NLR 家族含吡咯啉结构域蛋白 3 (NLRP3) 炎性体的激活,并能抑制阿尔茨海默氏症患者体内小胶质细胞和星形胶质细胞的激活。然而,人们对低密度脂蛋白受体对缺血性脑卒中星形胶质细胞活化的影响知之甚少。为了解决这个问题,我们在本研究中探讨了低密度脂蛋白受体调节缺血性中风模型中星形胶质细胞极化的机制。首先,我们通过免疫荧光染色和 Western 印迹分析检测了低密度脂蛋白受体在星形胶质细胞中的表达。我们观察到在大脑中动脉闭塞再灌注和缺氧-葡萄糖/复氧后,低密度脂蛋白受体明显下调。其次,我们利用星形胶质细胞特异性腺相关病毒诱导星形胶质细胞特异性过表达低密度脂蛋白受体。在星形胶质细胞中过表达低密度脂蛋白受体可改善大脑中动脉闭塞小鼠的神经功能预后,并逆转神经毒性星形胶质细胞,形成神经保护表型。最后,我们发现过表达低密度脂蛋白受体可抑制氧-葡萄糖剥夺/复氧损伤星形胶质细胞中 NLRP3 炎性体的活化,而添加 NLRP3 激动剂尼格列汀可恢复神经毒性星形胶质细胞表型。这些发现表明,低密度脂蛋白受体可抑制NLRP3介导的星形胶质细胞神经毒性极化,增加星形胶质细胞中的低密度脂蛋白受体可能是治疗缺血性脑卒中的一种新策略。
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来源期刊
Neural Regeneration Research
Neural Regeneration Research CELL BIOLOGY-NEUROSCIENCES
CiteScore
8.00
自引率
9.80%
发文量
515
审稿时长
1.0 months
期刊介绍: Neural Regeneration Research (NRR) is the Open Access journal specializing in neural regeneration and indexed by SCI-E and PubMed. The journal is committed to publishing articles on basic pathobiology of injury, repair and protection to the nervous system, while considering preclinical and clinical trials targeted at improving traumatically injuried patients and patients with neurodegenerative diseases.
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