LRP1型
髓鞘
吞噬作用
星形胶质细胞
白质
细胞生物学
生物
基因敲除
髓鞘碱性蛋白
小胶质细胞
神经科学
医学
病理
中枢神经系统
免疫学
脂蛋白
内分泌学
炎症
磁共振成像
低密度脂蛋白受体
生物化学
基因
放射科
胆固醇
作者
Ting Wan,Wusheng Zhu,Ying Zhao,Xiaohao Zhang,Ruidong Ye,Meng Zuo,Pengfei Xu,Zhenqian Huang,Chen‐Yu Zhang,Yi Xie,Xinfeng Liu
标识
DOI:10.1038/s41467-022-28777-9
摘要
Abstract Ischemic stroke can cause secondary myelin damage in the white matter distal to the primary injury site. The contribution of astrocytes during secondary demyelination and the underlying mechanisms are unclear. Here, using a mouse of distal middle cerebral artery occlusion, we show that lipocalin-2 (LCN2), enriched in reactive astrocytes, expression increases in nonischemic areas of the corpus callosum upon injury. LCN2-expressing astrocytes acquire a phagocytic phenotype and are able to uptake myelin. Myelin removal is impaired in Lcn2 −/− astrocytes. Inducing re-expression of truncated LCN2(Δ2–20) in astrocytes restores phagocytosis and leads to progressive demyelination in Lcn2 −/− mice. Co-immunoprecipitation experiments show that LCN2 binds to low-density lipoprotein receptor-related protein 1 (LRP1) in astrocytes. Knockdown of Lrp1 reduces LCN2-induced myelin engulfment by astrocytes and reduces demyelination. Altogether, our findings suggest that LCN2/LRP1 regulates astrocyte-mediated myelin phagocytosis in a mouse model of ischemic stroke.
科研通智能强力驱动
Strongly Powered by AbleSci AI