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Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection

Vertical transmission of the intracellular parasite Toxoplasma gondii (T. gondii) can lead to devastating consequences during gestation. Tim-3, a negative immune regulator, is constitutively expressed on decidual macrophages, but its specific role during T. gondii infection has not yet been explored...

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Autores principales: Zhang, Dan, Ren, Liqin, Zhao, Mingdong, Yang, Chunyan, Liu, Xianbing, Zhang, Haixia, Jiang, Yuzhu, Sun, Xinyue, Li, Teng, Cui, Lijun, Hu, Xuemei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637377/
https://www.ncbi.nlm.nih.gov/pubmed/31354713
http://dx.doi.org/10.3389/fimmu.2019.01550
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author Zhang, Dan
Ren, Liqin
Zhao, Mingdong
Yang, Chunyan
Liu, Xianbing
Zhang, Haixia
Jiang, Yuzhu
Sun, Xinyue
Li, Teng
Cui, Lijun
Hu, Xuemei
author_facet Zhang, Dan
Ren, Liqin
Zhao, Mingdong
Yang, Chunyan
Liu, Xianbing
Zhang, Haixia
Jiang, Yuzhu
Sun, Xinyue
Li, Teng
Cui, Lijun
Hu, Xuemei
author_sort Zhang, Dan
collection PubMed
description Vertical transmission of the intracellular parasite Toxoplasma gondii (T. gondii) can lead to devastating consequences during gestation. Tim-3, a negative immune regulator, is constitutively expressed on decidual macrophages, but its specific role during T. gondii infection has not yet been explored. In the present study, we discovered that Tim-3 plays an important role in the abnormal pregnancy due to T. gondii infection using Tim-3(−/−) pregnant mice and anti-Tim-3 neutralizing antibody treated human decidual macrophages. The results showed that abnormal pregnancy outcomes were more prevalent in Tim-3(−/−) infected pregnant mice than in wild-type infected pregnant mice. Tim-3 expression in decidual macrophages was significantly down-regulated after T. gondii infection both in vitro and in vivo. Tim-3 down-regulation by T.gondii infection could strengthen M1 activation and weaken M2 tolerance by changing the M1 and M2 membrane molecule expression, arginine metabolic enzymes synthesis, and cytokine secretion profiles of decidual macrophages. Moreover, Tim-3 down-regulation by T.gondii infection led to PI3K-AKT phosphorylation inhibition, downstream transcription factor C/EBPβ expression, and SOCS1 activation, which resulted in enzymes synthesis regulation and cytokines secretion. Our study demonstrates that Tim-3 plays an indispensable role in the adverse pregnancy outcomes caused by T. gondii infection.
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spelling pubmed-66373772019-07-26 Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection Zhang, Dan Ren, Liqin Zhao, Mingdong Yang, Chunyan Liu, Xianbing Zhang, Haixia Jiang, Yuzhu Sun, Xinyue Li, Teng Cui, Lijun Hu, Xuemei Front Immunol Immunology Vertical transmission of the intracellular parasite Toxoplasma gondii (T. gondii) can lead to devastating consequences during gestation. Tim-3, a negative immune regulator, is constitutively expressed on decidual macrophages, but its specific role during T. gondii infection has not yet been explored. In the present study, we discovered that Tim-3 plays an important role in the abnormal pregnancy due to T. gondii infection using Tim-3(−/−) pregnant mice and anti-Tim-3 neutralizing antibody treated human decidual macrophages. The results showed that abnormal pregnancy outcomes were more prevalent in Tim-3(−/−) infected pregnant mice than in wild-type infected pregnant mice. Tim-3 expression in decidual macrophages was significantly down-regulated after T. gondii infection both in vitro and in vivo. Tim-3 down-regulation by T.gondii infection could strengthen M1 activation and weaken M2 tolerance by changing the M1 and M2 membrane molecule expression, arginine metabolic enzymes synthesis, and cytokine secretion profiles of decidual macrophages. Moreover, Tim-3 down-regulation by T.gondii infection led to PI3K-AKT phosphorylation inhibition, downstream transcription factor C/EBPβ expression, and SOCS1 activation, which resulted in enzymes synthesis regulation and cytokines secretion. Our study demonstrates that Tim-3 plays an indispensable role in the adverse pregnancy outcomes caused by T. gondii infection. Frontiers Media S.A. 2019-07-11 /pmc/articles/PMC6637377/ /pubmed/31354713 http://dx.doi.org/10.3389/fimmu.2019.01550 Text en Copyright © 2019 Zhang, Ren, Zhao, Yang, Liu, Zhang, Jiang, Sun, Li, Cui and Hu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Dan
Ren, Liqin
Zhao, Mingdong
Yang, Chunyan
Liu, Xianbing
Zhang, Haixia
Jiang, Yuzhu
Sun, Xinyue
Li, Teng
Cui, Lijun
Hu, Xuemei
Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection
title Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection
title_full Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection
title_fullStr Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection
title_full_unstemmed Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection
title_short Role of Tim-3 in Decidual Macrophage Functional Polarization During Abnormal Pregnancy With Toxoplasma gondii Infection
title_sort role of tim-3 in decidual macrophage functional polarization during abnormal pregnancy with toxoplasma gondii infection
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637377/
https://www.ncbi.nlm.nih.gov/pubmed/31354713
http://dx.doi.org/10.3389/fimmu.2019.01550
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