Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells

Microplastics (< 5 mm diameter) are one of most important environmental pollutants and contaminants worldwide. However, how microplastics affect liver immune microenvironment in not well understood. Microplastics (0.5 µm) were administered orally to C57BL/6J mice for 4 consecutive weeks at the ra...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Liangtao Zhao, Wenyuan Shi, Fangfang Hu, Xujun Song, Zhangjun Cheng, Jiahua Zhou
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://doaj.org/article/49ea15201a694cb6966fa4d168902318
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:49ea15201a694cb6966fa4d168902318
record_format dspace
spelling oai:doaj.org-article:49ea15201a694cb6966fa4d1689023182021-11-06T04:14:30ZProlonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells0147-651310.1016/j.ecoenv.2021.112882https://doaj.org/article/49ea15201a694cb6966fa4d1689023182021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0147651321009945https://doaj.org/toc/0147-6513Microplastics (< 5 mm diameter) are one of most important environmental pollutants and contaminants worldwide. However, how microplastics affect liver immune microenvironment in not well understood. Microplastics (0.5 µm) were administered orally to C57BL/6J mice for 4 consecutive weeks at the rate of 0.5 mg/day. Non-parenchymal cells were isolated from of the mice through fractionation of fresh hepatic tissues. The immune landscape for four cell populations of B cells, T cells, NK cells and macrophages in the liver tissues was then evaluated using flow cytometry. The secretion level of inflammatory cytokines and associated signaling pathway were investigated using quantitative real-time polymerase chain reaction and western blot. Oral ingestion of microplastics increases liver weight, general liver index as well as expression of serum, liver function-related indicators. Microplastics also increased the infiltration of natural killer cells and macrophages to non-parenchymal liver cells, but reduced that of B cells to the same tissues. However, microplastics had no effect on the infiltration of T cell to non-parenchymal liver cells. Ingestion of MPs also up-regulated the expression of IFN-γ, TNF-α, IL-1β, IL-6 and IL-33 mRNA, but down-regulated that of IL-4, IL-5, IL-10, IL-18 and TGF-β1. Overall, the aforementioned processes were regulated via the NF-κB pathway in the hepatic non-parenchymal cells. Microplastics disrupts inflammatory process in liver tissues via the NF-κB signaling pathway. These findings provide a strong foundation on immune processes in hepatic tissues following prolonged ingestion of microplastics.Liangtao ZhaoWenyuan ShiFangfang HuXujun SongZhangjun ChengJiahua ZhouElsevierarticleMicroplasticsMacrophagesNatural killerInflammationLiverEnvironmental pollutionTD172-193.5Environmental sciencesGE1-350ENEcotoxicology and Environmental Safety, Vol 227, Iss , Pp 112882- (2021)
institution DOAJ
collection DOAJ
language EN
topic Microplastics
Macrophages
Natural killer
Inflammation
Liver
Environmental pollution
TD172-193.5
Environmental sciences
GE1-350
spellingShingle Microplastics
Macrophages
Natural killer
Inflammation
Liver
Environmental pollution
TD172-193.5
Environmental sciences
GE1-350
Liangtao Zhao
Wenyuan Shi
Fangfang Hu
Xujun Song
Zhangjun Cheng
Jiahua Zhou
Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells
description Microplastics (< 5 mm diameter) are one of most important environmental pollutants and contaminants worldwide. However, how microplastics affect liver immune microenvironment in not well understood. Microplastics (0.5 µm) were administered orally to C57BL/6J mice for 4 consecutive weeks at the rate of 0.5 mg/day. Non-parenchymal cells were isolated from of the mice through fractionation of fresh hepatic tissues. The immune landscape for four cell populations of B cells, T cells, NK cells and macrophages in the liver tissues was then evaluated using flow cytometry. The secretion level of inflammatory cytokines and associated signaling pathway were investigated using quantitative real-time polymerase chain reaction and western blot. Oral ingestion of microplastics increases liver weight, general liver index as well as expression of serum, liver function-related indicators. Microplastics also increased the infiltration of natural killer cells and macrophages to non-parenchymal liver cells, but reduced that of B cells to the same tissues. However, microplastics had no effect on the infiltration of T cell to non-parenchymal liver cells. Ingestion of MPs also up-regulated the expression of IFN-γ, TNF-α, IL-1β, IL-6 and IL-33 mRNA, but down-regulated that of IL-4, IL-5, IL-10, IL-18 and TGF-β1. Overall, the aforementioned processes were regulated via the NF-κB pathway in the hepatic non-parenchymal cells. Microplastics disrupts inflammatory process in liver tissues via the NF-κB signaling pathway. These findings provide a strong foundation on immune processes in hepatic tissues following prolonged ingestion of microplastics.
format article
author Liangtao Zhao
Wenyuan Shi
Fangfang Hu
Xujun Song
Zhangjun Cheng
Jiahua Zhou
author_facet Liangtao Zhao
Wenyuan Shi
Fangfang Hu
Xujun Song
Zhangjun Cheng
Jiahua Zhou
author_sort Liangtao Zhao
title Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells
title_short Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells
title_full Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells
title_fullStr Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells
title_full_unstemmed Prolonged oral ingestion of microplastics induced inflammation in the liver tissues of C57BL/6J mice through polarization of macrophages and increased infiltration of natural killer cells
title_sort prolonged oral ingestion of microplastics induced inflammation in the liver tissues of c57bl/6j mice through polarization of macrophages and increased infiltration of natural killer cells
publisher Elsevier
publishDate 2021
url https://doaj.org/article/49ea15201a694cb6966fa4d168902318
work_keys_str_mv AT liangtaozhao prolongedoralingestionofmicroplasticsinducedinflammationinthelivertissuesofc57bl6jmicethroughpolarizationofmacrophagesandincreasedinfiltrationofnaturalkillercells
AT wenyuanshi prolongedoralingestionofmicroplasticsinducedinflammationinthelivertissuesofc57bl6jmicethroughpolarizationofmacrophagesandincreasedinfiltrationofnaturalkillercells
AT fangfanghu prolongedoralingestionofmicroplasticsinducedinflammationinthelivertissuesofc57bl6jmicethroughpolarizationofmacrophagesandincreasedinfiltrationofnaturalkillercells
AT xujunsong prolongedoralingestionofmicroplasticsinducedinflammationinthelivertissuesofc57bl6jmicethroughpolarizationofmacrophagesandincreasedinfiltrationofnaturalkillercells
AT zhangjuncheng prolongedoralingestionofmicroplasticsinducedinflammationinthelivertissuesofc57bl6jmicethroughpolarizationofmacrophagesandincreasedinfiltrationofnaturalkillercells
AT jiahuazhou prolongedoralingestionofmicroplasticsinducedinflammationinthelivertissuesofc57bl6jmicethroughpolarizationofmacrophagesandincreasedinfiltrationofnaturalkillercells
_version_ 1718443913871622144