Cargando…
Phenotypic switch of human and mouse macrophages and resultant effects on apoptosis resistance in hepatocytes
Acute-on-chronic liver failure (ACLF) carries a significant burden on critical care services and health care resources. However, the exact pathogenesis of ACLF remains to be elucidated, and novel treatments are desperately required. In our previous work, we utilized mice subjected to acute insult in...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830937/ https://www.ncbi.nlm.nih.gov/pubmed/30803296 http://dx.doi.org/10.1177/1753425919831350 |
_version_ | 1783465862876889088 |
---|---|
author | Bai, Li Chen, Yu Zheng, Sujun Ren, Feng Kong, Ming Liu, Shuang Han, Yuanping Duan, Zhongping |
author_facet | Bai, Li Chen, Yu Zheng, Sujun Ren, Feng Kong, Ming Liu, Shuang Han, Yuanping Duan, Zhongping |
author_sort | Bai, Li |
collection | PubMed |
description | Acute-on-chronic liver failure (ACLF) carries a significant burden on critical care services and health care resources. However, the exact pathogenesis of ACLF remains to be elucidated, and novel treatments are desperately required. In our previous work, we utilized mice subjected to acute insult in the context of hepatic fibrosis to simulate the development of ACLF and documented the favorable hepatoprotection conferred by M2-like macrophages in vivo and in vitro. In the present study, we focused on the phenotypic switch of human and mouse macrophages and assessed the effects of this switch on apoptosis resistance in hepatocytes. For this purpose, human and mouse macrophages were isolated and polarized into M0, M(IFN-γ), M(IFN-γ→IL-4), M(IL-4) or M(IL-4→IFN-γ) subsets. Conditioned media (CM) from these subsets were applied to human and mouse hepatocytes followed by apoptosis induction. Cell apoptosis was evaluated by immunostaining for cleaved caspase-3. As a result, M(IFN-γ) or M(IL-4) macrophages switched their phenotype into M(IFN-γ→IL-4) or M(IL-4→IFN-γ) through reprogramming with IL-4 or IFN-γ, respectively. Importantly, hepatocytes pre-treated with M(IFN-γ→IL-4) CMs exhibited much weaker expression of cleaved caspase-3, compared to those pre-treated with M(IFN-γ) CM, and vice versa. Together, phenotypic switch of macrophages toward M(IL-4) phenotype confers hepatocytes enhanced resistance to apoptosis. |
format | Online Article Text |
id | pubmed-6830937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-68309372019-11-20 Phenotypic switch of human and mouse macrophages and resultant effects on apoptosis resistance in hepatocytes Bai, Li Chen, Yu Zheng, Sujun Ren, Feng Kong, Ming Liu, Shuang Han, Yuanping Duan, Zhongping Innate Immun Original Articles Acute-on-chronic liver failure (ACLF) carries a significant burden on critical care services and health care resources. However, the exact pathogenesis of ACLF remains to be elucidated, and novel treatments are desperately required. In our previous work, we utilized mice subjected to acute insult in the context of hepatic fibrosis to simulate the development of ACLF and documented the favorable hepatoprotection conferred by M2-like macrophages in vivo and in vitro. In the present study, we focused on the phenotypic switch of human and mouse macrophages and assessed the effects of this switch on apoptosis resistance in hepatocytes. For this purpose, human and mouse macrophages were isolated and polarized into M0, M(IFN-γ), M(IFN-γ→IL-4), M(IL-4) or M(IL-4→IFN-γ) subsets. Conditioned media (CM) from these subsets were applied to human and mouse hepatocytes followed by apoptosis induction. Cell apoptosis was evaluated by immunostaining for cleaved caspase-3. As a result, M(IFN-γ) or M(IL-4) macrophages switched their phenotype into M(IFN-γ→IL-4) or M(IL-4→IFN-γ) through reprogramming with IL-4 or IFN-γ, respectively. Importantly, hepatocytes pre-treated with M(IFN-γ→IL-4) CMs exhibited much weaker expression of cleaved caspase-3, compared to those pre-treated with M(IFN-γ) CM, and vice versa. Together, phenotypic switch of macrophages toward M(IL-4) phenotype confers hepatocytes enhanced resistance to apoptosis. SAGE Publications 2019-02-25 2019-04 /pmc/articles/PMC6830937/ /pubmed/30803296 http://dx.doi.org/10.1177/1753425919831350 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Bai, Li Chen, Yu Zheng, Sujun Ren, Feng Kong, Ming Liu, Shuang Han, Yuanping Duan, Zhongping Phenotypic switch of human and mouse macrophages and resultant effects on apoptosis resistance in hepatocytes |
title | Phenotypic switch of human and mouse macrophages and resultant
effects on apoptosis resistance in hepatocytes |
title_full | Phenotypic switch of human and mouse macrophages and resultant
effects on apoptosis resistance in hepatocytes |
title_fullStr | Phenotypic switch of human and mouse macrophages and resultant
effects on apoptosis resistance in hepatocytes |
title_full_unstemmed | Phenotypic switch of human and mouse macrophages and resultant
effects on apoptosis resistance in hepatocytes |
title_short | Phenotypic switch of human and mouse macrophages and resultant
effects on apoptosis resistance in hepatocytes |
title_sort | phenotypic switch of human and mouse macrophages and resultant
effects on apoptosis resistance in hepatocytes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830937/ https://www.ncbi.nlm.nih.gov/pubmed/30803296 http://dx.doi.org/10.1177/1753425919831350 |
work_keys_str_mv | AT baili phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT chenyu phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT zhengsujun phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT renfeng phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT kongming phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT liushuang phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT hanyuanping phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes AT duanzhongping phenotypicswitchofhumanandmousemacrophagesandresultanteffectsonapoptosisresistanceinhepatocytes |