炎症体
纳米材料
纳米医学
NLRC4型
钴
目标2
先天免疫系统
免疫系统
化学
炎症
细胞生物学
癌症研究
材料科学
免疫学
纳米技术
纳米颗粒
医学
生物
半胱氨酸蛋白酶1
无机化学
作者
Jun Lin,Liang Dong,Yiming Liu,Yi Hu,Chen Jiang,Ke Liu,Liu Liu,Yonghong Song,Mei Sun,Xing-Cheng Xiang,Kun Qu,Lu Yang,Longping Wen,Shu‐Hong Yu
摘要
ABSTRACT Activation of inflammasomes—immune system receptor sensor complexes that selectively activate inflammatory responses—has been associated with diverse human diseases, and many nanomedicine studies have reported that structurally and chemically diverse inorganic nanomaterials cause excessive inflammasome activation. Here, in stark contrast to reports of other inorganic nanomaterials, we find that nickel-cobalt alloy magnetic nanocrystals (NiCo NCs) actually inhibit activation of NLRP3, NLRC4 and AIM2 inflammasomes. We show that NiCo NCs disrupt the canonical inflammasome ASC speck formation process by downregulating the lncRNA Neat1, and experimentally confirm that the entry of NiCo NCs into cells is required for the observed inhibition of inflammasome activation. Furthermore, we find that NiCo NCs inhibit neutrophil recruitment in an acute peritonitis mouse model and relieve symptoms in a colitis mouse model, again by inhibiting inflammasome activation. Beyond demonstrating a highly surprising and apparently therapeutic impact for an inorganic nanomaterial on inflammatory responses, our work suggests that nickel- and cobalt-containing nanomaterials may offer an opportunity to design anti-inflammatory nanomedicines for the therapeutics of macrophage-mediated diseases.
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