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Apolipoprotein E ε4/4 genotype limits response to dietary induction of hyperhomocysteinemia and resulting inflammatory signaling.载脂蛋白 E ε4/4 基因型限制了对饮食诱导的高同型半胱氨酸血症和由此产生的炎症信号的反应。
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生长停滞特异性蛋白 6 减轻实验性缺血性中风后的白质损伤。

Growth arrest specific protein 6 alleviated white matter injury after experimental ischemic stroke.

机构信息

Department of Neurology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Department of Neurology, Nanjing Drum Tower Hospital Clinical College of Jiangsu University, Zhenjiang, China.

出版信息

J Cereb Blood Flow Metab. 2024 Jan;44(1):77-93. doi: 10.1177/0271678X231205078. Epub 2023 Oct 5.

DOI:10.1177/0271678X231205078
PMID:37794790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10905636/
Abstract

Ischemic white matter injury leads to long-term neurological deficits and lacks effective medication. Growth arrest specific protein 6 (Gas6) clears myelin debris, which is hypothesized to promote white matter integrity in experimental stroke models. By the middle cerebral artery occlusion (MCAO) stroke model, we observed that Gas6 reduced infarcted volume and behavior deficits 4 weeks after MCAO. Compared with control mice, Gas6-treatment mice represented higher FA values in the ipsilateral external capsules by MRI DTI scan. The SMI32/MBP ratio of the ipsilateral cortex and striatum was profoundly alleviated by Gas6 administration. Gas6-treatment group manifested thicker myelin sheaths than the control group by electron microscopy. We observed that Gas6 mainly promoted OPC maturation, which was closely related to microglia. Mechanically, Gas6 accelerated microglia-mediated myelin debris clearance and cholesterol transport protein expression (, , , ) and , accordingly less myelin debris and lipid deposited in Gas6 treated stroke mice. HX531 (RXR inhibitor) administration mitigated the functions of Gas6 in speeding up debris clearance and cholesterol transport protein expression. Generally, we concluded that Gas6 cleared myelin debris and promoted cholesterol transportation protein expression through activating RXR, which could be one critical mechanism contributing to white matter repair after stroke.

摘要

缺血性白质损伤导致长期神经功能缺损,且缺乏有效药物。生长停滞特异性蛋白 6(Gas6)可清除髓鞘碎片,这被假设可促进实验性中风模型中的白质完整性。通过大脑中动脉闭塞(MCAO)中风模型,我们观察到 Gas6 可减少 MCAO 后 4 周的梗死体积和行为缺陷。与对照组相比,MRI-DTI 扫描显示 Gas6 治疗组的对侧外囊的 FA 值更高。Gas6 给药可显著减轻对侧皮质和纹状体的 SMI32/MBP 比值。电镜观察到 Gas6 治疗组的髓鞘较对照组更厚。我们观察到 Gas6 主要促进少突胶质细胞前体细胞(OPC)成熟,这与小胶质细胞密切相关。机械上,Gas6 加速了小胶质细胞介导的髓鞘碎片清除和胆固醇转运蛋白表达(、、、),从而导致 Gas6 处理的中风小鼠中髓鞘碎片和脂质沉积减少。HX531(RXR 抑制剂)给药减轻了 Gas6 在加速碎片清除和胆固醇转运蛋白表达方面的作用。总的来说,我们得出结论,Gas6 通过激活 RXR 清除髓鞘碎片并促进胆固醇转运蛋白表达,这可能是中风后白质修复的一个关键机制。