Aflatoxin B1-activated heterophil extracellular traps result in the immunotoxicity to liver and kidney in chickens.


Journal

Developmental and comparative immunology
ISSN: 1879-0089
Titre abrégé: Dev Comp Immunol
Pays: United States
ID NLM: 7708205

Informations de publication

Date de publication:
03 2022
Historique:
received: 28 06 2021
revised: 18 11 2021
accepted: 18 11 2021
pubmed: 29 11 2021
medline: 8 4 2022
entrez: 28 11 2021
Statut: ppublish

Résumé

Aflatoxin B1 (AFB1) is a mycotoxin with strong toxicity and play a large proportion in aspergillosis. Heterophil extracellular traps (HETs) was considered as an innate immune response of chickens to resist pathogens. AFB1 has been reported to trigger macrophages extracellular traps (METs) in THP-1 cells and RAW264.7 cells, but whether AFB1 could also activate HETs release, and the mechanism underlying AFB1-activated HETs in chicken remains unclear. In this study, we confirmed that AFB1could induce HETs release, which was a network of DNA-based structures consist of citrullinated histone 3 (citH3) and elastase. Meanwhile, AFB1-activated HETs rely on the glycolytic process to provide energy, NADPH oxidase and p38 signaling pathway. Moreover, it has been verified that AFB1-activated HETs release could significantly increase the biochemical indexes of liver (ALT and AST) and kidney (CRE and BUN) in serum. In addition, histopathological observation showed that AFB1 caused swelling, necrosis and vacuolation of hepatocytes in liver, and necrosis, exfoliated of nephrocyte in kidney. Further investigation demonstrated that AFB1 significantly decreased the levels of SOD and GSH-PX but increased the level of MDA, and meanwhile induced the mRNA expressions of TNF-α, IL-6 and IL-1β, iNOS, COX-2, NLRP3, caspase-1, caspase-3 and caspase-11. However, all these AFB1-induced biochemical indexes and histopathological changes were effectively alleviated by DNase I (the standard degradant for HETs). In conclusion, it has preliminary confirmed that AFB1-activated HETs formation contributed to the immunotoxicity in chicken and provide new strategies for the therapy in aspergillosis.

Identifiants

pubmed: 34838609
pii: S0145-305X(21)00333-5
doi: 10.1016/j.dci.2021.104325
pii:
doi:

Substances chimiques

Aflatoxin B1 9N2N2Y55MH

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

104325

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Xinxin Gao (X)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Liqiang Jiang (L)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Jingnan Xu (J)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Wei Liu (W)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Shurou Li (S)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Wenlong Huang (W)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Haiguang Zhao (H)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Zhengtao Yang (Z)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China.

Xingang Yu (X)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China. Electronic address: yuxingang4525@163.com.

Zhengkai Wei (Z)

College of Life Sciences and Engineering, Foshan University, Foshan, 528225, Guangdong Province, PR China. Electronic address: wei_zhengkai@126.com.

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Classifications MeSH