Chlorpyrifos Suppresses Neutrophil Extracellular Traps in Carp by Promoting Necroptosis and Inhibiting Respiratory Burst Caused by the PKCMAPK Pathway

Joint Authors

Xu, S. W.
Zhang, Qiaojian
Wang, Shengchen
Zheng, Shufang
Zhang, Ziwei

Source

Oxidative Medicine and Cellular Longevity

Issue

Vol. 2019, Issue 2019 (31 Dec. 2019), pp.1-11, 11 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2019-02-07

Country of Publication

Egypt

No. of Pages

11

Main Subjects

Biology

Abstract EN

Neutrophil extracellular traps (NETs) are reticular structures formed by myeloperoxidase (MPO), histones, and neutrophil elastase (NE) that are released from neutrophils in response to pathogenic stimuli.

Chlorpyrifos (CPF) is wildly used as an organophosphorus pesticide that causes a range of toxicological and environmental problems.

Exposure to CPF can increase the production of neutrophils in carps, and this increase can be considered a biomarker of water pollution.

To explore a relationship between NETs and CPF and its mechanism of influence, we treated neutrophils from the blood of carp with 1 μg/mL phorbol 12-myristate 13-acetate (PMA), 0.325 mg/L CPF, or 20 μM necrostatin-1 (Nec-1).

The production of MPO and NETs was reduced in the CPF+PMA group compared with that in the PMA group.

CPF can cause an increase in reactive oxygen species (ROS), while inhibiting respiratory burst caused by PMA stimulation.

We found that the expression levels of protein-coupled receptor 84 (gpr84), dystroglycan (DAG), proto-oncogene serine/threonine kinase (RAF), protein kinase C (PKC), and mitogen-activated protein kinase 3 (MAPK3) in the CPF+PMA group were lower than those in the PMA group, indicating that the PKC-MAPK pathway was suppressed.

The expression levels of cylindromatosis (CYLD), mixed lineage kinase domain-like pseudokinase (MLKL), receptor-interacting serine-threonine kinase 1 (RIP1), and receptor-interacting serine-threonine kinase 3 (RIP3) were increased, and the expression levels of caspase 8 were reduced by CPF, indicating that CPF may cause necroptosis.

The addition of Nec-1 restored the number of NETs in the CPF+PMA group.

The results indicate that CPF reduced the production of NETs by inhibiting respiratory burst and increasing necroptosis.

The results contribute to the understanding of the immunotoxicological mechanism of CPF and provide a reference for comparative medical studies.

American Psychological Association (APA)

Zhang, Qiaojian& Wang, Shengchen& Zheng, Shufang& Zhang, Ziwei& Xu, S. W.. 2019. Chlorpyrifos Suppresses Neutrophil Extracellular Traps in Carp by Promoting Necroptosis and Inhibiting Respiratory Burst Caused by the PKCMAPK Pathway. Oxidative Medicine and Cellular Longevity،Vol. 2019, no. 2019, pp.1-11.
https://search.emarefa.net/detail/BIM-1202367

Modern Language Association (MLA)

Zhang, Qiaojian…[et al.]. Chlorpyrifos Suppresses Neutrophil Extracellular Traps in Carp by Promoting Necroptosis and Inhibiting Respiratory Burst Caused by the PKCMAPK Pathway. Oxidative Medicine and Cellular Longevity No. 2019 (2019), pp.1-11.
https://search.emarefa.net/detail/BIM-1202367

American Medical Association (AMA)

Zhang, Qiaojian& Wang, Shengchen& Zheng, Shufang& Zhang, Ziwei& Xu, S. W.. Chlorpyrifos Suppresses Neutrophil Extracellular Traps in Carp by Promoting Necroptosis and Inhibiting Respiratory Burst Caused by the PKCMAPK Pathway. Oxidative Medicine and Cellular Longevity. 2019. Vol. 2019, no. 2019, pp.1-11.
https://search.emarefa.net/detail/BIM-1202367

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1202367