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M1 Macrophages Are More Susceptible to Necroptosis
Macrophages play a crucial role in host innate immune defense against infection and tissue injury. Although macrophage activation and polarization has been well studied, we know less regarding the role of macrophage activation/polarization in inflammation-associated necrotic cell death. By using bon...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098744/ https://www.ncbi.nlm.nih.gov/pubmed/33959729 http://dx.doi.org/10.33696/immunology.3.084 |
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author | Hao, Qin Idell, Steven Tang, Hua |
author_facet | Hao, Qin Idell, Steven Tang, Hua |
author_sort | Hao, Qin |
collection | PubMed |
description | Macrophages play a crucial role in host innate immune defense against infection and tissue injury. Although macrophage activation and polarization has been well studied, we know less regarding the role of macrophage activation/polarization in inflammation-associated necrotic cell death. By using bone marrow-derived macrophages, we have recently demonstrated that M1 macrophages are much more susceptible than M0 and M2 subtypes of macrophages to necrotic cell death. Moreover, we showed that the enhanced necroptosis in M1 macrophages is dependent on the kinase activity of receptor-interacting protein kinase-3 (RIPK3) and may involve the upregulation of key necroptosis signaling molecules including RIPK3, mixed lineage kinase domain-like protein, and Z-DNA/ RNA binding protein 1. Our findings provide novel insights into the mechanisms of M1 macrophage engagement in inflammation and tissue injury. |
format | Online Article Text |
id | pubmed-8098744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-80987442021-05-05 M1 Macrophages Are More Susceptible to Necroptosis Hao, Qin Idell, Steven Tang, Hua J Cell Immunol Article Macrophages play a crucial role in host innate immune defense against infection and tissue injury. Although macrophage activation and polarization has been well studied, we know less regarding the role of macrophage activation/polarization in inflammation-associated necrotic cell death. By using bone marrow-derived macrophages, we have recently demonstrated that M1 macrophages are much more susceptible than M0 and M2 subtypes of macrophages to necrotic cell death. Moreover, we showed that the enhanced necroptosis in M1 macrophages is dependent on the kinase activity of receptor-interacting protein kinase-3 (RIPK3) and may involve the upregulation of key necroptosis signaling molecules including RIPK3, mixed lineage kinase domain-like protein, and Z-DNA/ RNA binding protein 1. Our findings provide novel insights into the mechanisms of M1 macrophage engagement in inflammation and tissue injury. 2021 /pmc/articles/PMC8098744/ /pubmed/33959729 http://dx.doi.org/10.33696/immunology.3.084 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Hao, Qin Idell, Steven Tang, Hua M1 Macrophages Are More Susceptible to Necroptosis |
title | M1 Macrophages Are More Susceptible to Necroptosis |
title_full | M1 Macrophages Are More Susceptible to Necroptosis |
title_fullStr | M1 Macrophages Are More Susceptible to Necroptosis |
title_full_unstemmed | M1 Macrophages Are More Susceptible to Necroptosis |
title_short | M1 Macrophages Are More Susceptible to Necroptosis |
title_sort | m1 macrophages are more susceptible to necroptosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8098744/ https://www.ncbi.nlm.nih.gov/pubmed/33959729 http://dx.doi.org/10.33696/immunology.3.084 |
work_keys_str_mv | AT haoqin m1macrophagesaremoresusceptibletonecroptosis AT idellsteven m1macrophagesaremoresusceptibletonecroptosis AT tanghua m1macrophagesaremoresusceptibletonecroptosis |