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You are what you eat and how you digest it! A discussion on inflammatory efferocytosis

Efferocytosis is a process by which phagocytes remove dead or dying cells. It is considered anti-inflammatory, as the removal process reduces potential inflammatory molecules originating from dead cells and results in the reprogramming of macrophages to an anti-inflammatory state. However, engulfmen...

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Detalles Bibliográficos
Autor principal: Tanzer, Maria C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947526/
https://www.ncbi.nlm.nih.gov/pubmed/36846584
http://dx.doi.org/10.3389/fcell.2023.1132696
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author Tanzer, Maria C.
author_facet Tanzer, Maria C.
author_sort Tanzer, Maria C.
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description Efferocytosis is a process by which phagocytes remove dead or dying cells. It is considered anti-inflammatory, as the removal process reduces potential inflammatory molecules originating from dead cells and results in the reprogramming of macrophages to an anti-inflammatory state. However, engulfment of infected dead cells, deregulated phagocytosis and perturbed digestion of apoptotic bodies induce inflammatory signalling pathways during efferocytosis. The affected inflammatory signalling molecules and the mechanism of activation are largely unknown. I discuss how the choice of dead cell cargo, the type of ingestion, and the digestion efficiency can influence phagocyte programming in the context of disease. I also present the latest findings, highlight knowledge gaps, and propose selected experimental approaches to fill them.
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spelling pubmed-99475262023-02-24 You are what you eat and how you digest it! A discussion on inflammatory efferocytosis Tanzer, Maria C. Front Cell Dev Biol Cell and Developmental Biology Efferocytosis is a process by which phagocytes remove dead or dying cells. It is considered anti-inflammatory, as the removal process reduces potential inflammatory molecules originating from dead cells and results in the reprogramming of macrophages to an anti-inflammatory state. However, engulfment of infected dead cells, deregulated phagocytosis and perturbed digestion of apoptotic bodies induce inflammatory signalling pathways during efferocytosis. The affected inflammatory signalling molecules and the mechanism of activation are largely unknown. I discuss how the choice of dead cell cargo, the type of ingestion, and the digestion efficiency can influence phagocyte programming in the context of disease. I also present the latest findings, highlight knowledge gaps, and propose selected experimental approaches to fill them. Frontiers Media S.A. 2023-02-09 /pmc/articles/PMC9947526/ /pubmed/36846584 http://dx.doi.org/10.3389/fcell.2023.1132696 Text en Copyright © 2023 Tanzer. https://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 Cell and Developmental Biology
Tanzer, Maria C.
You are what you eat and how you digest it! A discussion on inflammatory efferocytosis
title You are what you eat and how you digest it! A discussion on inflammatory efferocytosis
title_full You are what you eat and how you digest it! A discussion on inflammatory efferocytosis
title_fullStr You are what you eat and how you digest it! A discussion on inflammatory efferocytosis
title_full_unstemmed You are what you eat and how you digest it! A discussion on inflammatory efferocytosis
title_short You are what you eat and how you digest it! A discussion on inflammatory efferocytosis
title_sort you are what you eat and how you digest it! a discussion on inflammatory efferocytosis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947526/
https://www.ncbi.nlm.nih.gov/pubmed/36846584
http://dx.doi.org/10.3389/fcell.2023.1132696
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