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Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation

Phospholipases A(2)s (PLA(2)s) constitute one of the major protein groups present in the venoms of viperid and crotalid snakes. Snake venom PLA(2)s (svPLA(2)s) exhibit a remarkable functional diversity, as they have been described to induce a myriad of toxic effects. Local inflammation is an importa...

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Autores principales: Moreira, Vanessa, Leiguez, Elbio, Janovits, Priscila Motta, Maia-Marques, Rodrigo, Fernandes, Cristina Maria, Teixeira, Catarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709003/
https://www.ncbi.nlm.nih.gov/pubmed/34941706
http://dx.doi.org/10.3390/toxins13120868
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author Moreira, Vanessa
Leiguez, Elbio
Janovits, Priscila Motta
Maia-Marques, Rodrigo
Fernandes, Cristina Maria
Teixeira, Catarina
author_facet Moreira, Vanessa
Leiguez, Elbio
Janovits, Priscila Motta
Maia-Marques, Rodrigo
Fernandes, Cristina Maria
Teixeira, Catarina
author_sort Moreira, Vanessa
collection PubMed
description Phospholipases A(2)s (PLA(2)s) constitute one of the major protein groups present in the venoms of viperid and crotalid snakes. Snake venom PLA(2)s (svPLA(2)s) exhibit a remarkable functional diversity, as they have been described to induce a myriad of toxic effects. Local inflammation is an important characteristic of snakebite envenomation inflicted by viperid and crotalid species and diverse svPLA(2)s have been studied for their proinflammatory properties. Moreover, based on their molecular, structural, and functional properties, the viperid svPLA(2)s are classified into the group IIA secreted PLA(2)s, which encompasses mammalian inflammatory sPLA(2)s. Thus, research on svPLA(2)s has attained paramount importance for better understanding the role of this class of enzymes in snake envenomation and the participation of GIIA sPLA(2)s in pathophysiological conditions and for the development of new therapeutic agents. In this review, we highlight studies that have identified the inflammatory activities of svPLA(2)s, in particular, those from Bothrops genus snakes, which are major medically important snakes in Latin America, and we describe recent advances in our collective understanding of the mechanisms underlying their inflammatory effects. We also discuss studies that dissect the action of these venom enzymes in inflammatory cells focusing on molecular mechanisms and signaling pathways involved in the biosynthesis of lipid mediators and lipid accumulation in immunocompetent cells.
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spelling pubmed-87090032021-12-25 Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation Moreira, Vanessa Leiguez, Elbio Janovits, Priscila Motta Maia-Marques, Rodrigo Fernandes, Cristina Maria Teixeira, Catarina Toxins (Basel) Review Phospholipases A(2)s (PLA(2)s) constitute one of the major protein groups present in the venoms of viperid and crotalid snakes. Snake venom PLA(2)s (svPLA(2)s) exhibit a remarkable functional diversity, as they have been described to induce a myriad of toxic effects. Local inflammation is an important characteristic of snakebite envenomation inflicted by viperid and crotalid species and diverse svPLA(2)s have been studied for their proinflammatory properties. Moreover, based on their molecular, structural, and functional properties, the viperid svPLA(2)s are classified into the group IIA secreted PLA(2)s, which encompasses mammalian inflammatory sPLA(2)s. Thus, research on svPLA(2)s has attained paramount importance for better understanding the role of this class of enzymes in snake envenomation and the participation of GIIA sPLA(2)s in pathophysiological conditions and for the development of new therapeutic agents. In this review, we highlight studies that have identified the inflammatory activities of svPLA(2)s, in particular, those from Bothrops genus snakes, which are major medically important snakes in Latin America, and we describe recent advances in our collective understanding of the mechanisms underlying their inflammatory effects. We also discuss studies that dissect the action of these venom enzymes in inflammatory cells focusing on molecular mechanisms and signaling pathways involved in the biosynthesis of lipid mediators and lipid accumulation in immunocompetent cells. MDPI 2021-12-04 /pmc/articles/PMC8709003/ /pubmed/34941706 http://dx.doi.org/10.3390/toxins13120868 Text en © 2021 by the authors. 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 Review
Moreira, Vanessa
Leiguez, Elbio
Janovits, Priscila Motta
Maia-Marques, Rodrigo
Fernandes, Cristina Maria
Teixeira, Catarina
Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
title Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
title_full Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
title_fullStr Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
title_full_unstemmed Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
title_short Inflammatory Effects of Bothrops Phospholipases A(2): Mechanisms Involved in Biosynthesis of Lipid Mediators and Lipid Accumulation
title_sort inflammatory effects of bothrops phospholipases a(2): mechanisms involved in biosynthesis of lipid mediators and lipid accumulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709003/
https://www.ncbi.nlm.nih.gov/pubmed/34941706
http://dx.doi.org/10.3390/toxins13120868
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