Nickle-cobalt alloy nanocrystals inhibit activation of inflammasomes

Author:

Lin Jun1,Dong Liang12,Liu Yi-Ming1,Hu Yi1,Jiang Chen1,Liu Ke1,Liu Liu1,Song Yong-Hong3,Sun Mei1,Xiang Xing-Cheng4,Qu Kun15ORCID,Lu Yang3,Wen Long-Ping1,Yu Shu-Hong1ORCID

Affiliation:

1. Department of Neurosurgery, The First Affiliated Hospital of USTC, School of Basic Medical Sciences, Division of Molecular Medicine, Department of Chemistry, Institute of Biomimetic Materials & Chemistry, Division of Nanomaterials & Chemistry, Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China , Hefei 230027 , China

2. The Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences , Hangzhou 310022 , China

3. Anhui Province Key Laboratory of Advanced Catalytic Materials and Reaction Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology , Hefei 230009 , China

4. The WUT-AMU Franco-Chinese Institute, Wuhan University of Technology , Wuhan 430070 , China

5. Institute of Artificial Intelligence, Hefei Comprehensive National Science Center , Hefei 230027 , China

Abstract

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.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hefei, China

Fundamental Research Funds for the Central Universities

National Key Research and Development Program of China

China Postdoctoral Science Foundation

University Synergy Innovation Program of Anhui Province

Science and Technology Major Project of Anhui Province

Natural Science Foundation of Anhui Province

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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