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Innate Immune Programing by Endotoxin and Its Pathological Consequences

Monocytes and macrophages play pivotal roles in inflammation and homeostasis. Recent studies suggest that dynamic programing of macrophages and monocytes may give rise to distinct “memory” states. Lipopolysaccharide (LPS), a classical pattern recognition molecule, dynamically programs innate immune...

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Detalles Bibliográficos
Autores principales: Morris, Matthew C., Gilliam, Elizabeth A., Li, Liwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285116/
https://www.ncbi.nlm.nih.gov/pubmed/25610440
http://dx.doi.org/10.3389/fimmu.2014.00680
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author Morris, Matthew C.
Gilliam, Elizabeth A.
Li, Liwu
author_facet Morris, Matthew C.
Gilliam, Elizabeth A.
Li, Liwu
author_sort Morris, Matthew C.
collection PubMed
description Monocytes and macrophages play pivotal roles in inflammation and homeostasis. Recent studies suggest that dynamic programing of macrophages and monocytes may give rise to distinct “memory” states. Lipopolysaccharide (LPS), a classical pattern recognition molecule, dynamically programs innate immune responses. Emerging studies have revealed complex dynamics of cellular responses to LPS, with high doses causing acute, resolving inflammation, while lower doses are associated with low-grade and chronic non-resolving inflammation. These phenomena hint at dynamic complexities of intra-cellular signaling circuits downstream of the Toll-like receptor 4 (TLR4). In this review, we examine pathological effects of varying LPS doses with respect to the dynamics of innate immune responses and key molecular regulatory circuits responsible for these effects.
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spelling pubmed-42851162015-01-21 Innate Immune Programing by Endotoxin and Its Pathological Consequences Morris, Matthew C. Gilliam, Elizabeth A. Li, Liwu Front Immunol Immunology Monocytes and macrophages play pivotal roles in inflammation and homeostasis. Recent studies suggest that dynamic programing of macrophages and monocytes may give rise to distinct “memory” states. Lipopolysaccharide (LPS), a classical pattern recognition molecule, dynamically programs innate immune responses. Emerging studies have revealed complex dynamics of cellular responses to LPS, with high doses causing acute, resolving inflammation, while lower doses are associated with low-grade and chronic non-resolving inflammation. These phenomena hint at dynamic complexities of intra-cellular signaling circuits downstream of the Toll-like receptor 4 (TLR4). In this review, we examine pathological effects of varying LPS doses with respect to the dynamics of innate immune responses and key molecular regulatory circuits responsible for these effects. Frontiers Media S.A. 2015-01-06 /pmc/articles/PMC4285116/ /pubmed/25610440 http://dx.doi.org/10.3389/fimmu.2014.00680 Text en Copyright © 2015 Morris, Gilliam and Li. 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) or licensor 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
Morris, Matthew C.
Gilliam, Elizabeth A.
Li, Liwu
Innate Immune Programing by Endotoxin and Its Pathological Consequences
title Innate Immune Programing by Endotoxin and Its Pathological Consequences
title_full Innate Immune Programing by Endotoxin and Its Pathological Consequences
title_fullStr Innate Immune Programing by Endotoxin and Its Pathological Consequences
title_full_unstemmed Innate Immune Programing by Endotoxin and Its Pathological Consequences
title_short Innate Immune Programing by Endotoxin and Its Pathological Consequences
title_sort innate immune programing by endotoxin and its pathological consequences
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285116/
https://www.ncbi.nlm.nih.gov/pubmed/25610440
http://dx.doi.org/10.3389/fimmu.2014.00680
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