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Deciphering Complex Interactions in Bioactive Lipid Signaling

Lipids are usually viewed as metabolic fuel and structural membrane components. Yet, in recent years, different families of lipids able to act as authentic messengers between cells and/or intracellularly have been discovered. Such lipid signals have been shown to exert their biological activity via...

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Autor principal: Maccarrone, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057854/
https://www.ncbi.nlm.nih.gov/pubmed/36985594
http://dx.doi.org/10.3390/molecules28062622
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author Maccarrone, Mauro
author_facet Maccarrone, Mauro
author_sort Maccarrone, Mauro
collection PubMed
description Lipids are usually viewed as metabolic fuel and structural membrane components. Yet, in recent years, different families of lipids able to act as authentic messengers between cells and/or intracellularly have been discovered. Such lipid signals have been shown to exert their biological activity via specific receptors that, by triggering distinct signal transduction pathways, regulate manifold pathophysiological processes in our body. Here, endogenous bioactive lipids produced from arachidonic acid (AA) and other poly-unsaturated fatty acids will be presented, in order to put into better perspective the relevance of their mutual interactions for health and disease conditions. To this end, metabolism and signal transduction pathways of classical eicosanoids, endocannabinoids and specialized pro-resolving mediators will be described, and the intersections and commonalities of their metabolic enzymes and binding receptors will be discussed. Moreover, the interactions of AA-derived signals with other bioactive lipids such as shingosine-1-phosphate and steroid hormones will be addressed.
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spelling pubmed-100578542023-03-30 Deciphering Complex Interactions in Bioactive Lipid Signaling Maccarrone, Mauro Molecules Perspective Lipids are usually viewed as metabolic fuel and structural membrane components. Yet, in recent years, different families of lipids able to act as authentic messengers between cells and/or intracellularly have been discovered. Such lipid signals have been shown to exert their biological activity via specific receptors that, by triggering distinct signal transduction pathways, regulate manifold pathophysiological processes in our body. Here, endogenous bioactive lipids produced from arachidonic acid (AA) and other poly-unsaturated fatty acids will be presented, in order to put into better perspective the relevance of their mutual interactions for health and disease conditions. To this end, metabolism and signal transduction pathways of classical eicosanoids, endocannabinoids and specialized pro-resolving mediators will be described, and the intersections and commonalities of their metabolic enzymes and binding receptors will be discussed. Moreover, the interactions of AA-derived signals with other bioactive lipids such as shingosine-1-phosphate and steroid hormones will be addressed. MDPI 2023-03-14 /pmc/articles/PMC10057854/ /pubmed/36985594 http://dx.doi.org/10.3390/molecules28062622 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Perspective
Maccarrone, Mauro
Deciphering Complex Interactions in Bioactive Lipid Signaling
title Deciphering Complex Interactions in Bioactive Lipid Signaling
title_full Deciphering Complex Interactions in Bioactive Lipid Signaling
title_fullStr Deciphering Complex Interactions in Bioactive Lipid Signaling
title_full_unstemmed Deciphering Complex Interactions in Bioactive Lipid Signaling
title_short Deciphering Complex Interactions in Bioactive Lipid Signaling
title_sort deciphering complex interactions in bioactive lipid signaling
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057854/
https://www.ncbi.nlm.nih.gov/pubmed/36985594
http://dx.doi.org/10.3390/molecules28062622
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