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NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases

Virtually all types of cardiovascular diseases are associated with pathological activation of the innate immune system. The NACHT, leucine-rich repeat (LRR), and pyrin domain (PYD)-containing protein 3 (NLRP3) inflammasome is a protein complex that functions as a platform for rapid induction of the...

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Autores principales: Mezzaroma, Eleonora, Abbate, Antonio, Toldo, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917621/
https://www.ncbi.nlm.nih.gov/pubmed/33673188
http://dx.doi.org/10.3390/molecules26040976
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author Mezzaroma, Eleonora
Abbate, Antonio
Toldo, Stefano
author_facet Mezzaroma, Eleonora
Abbate, Antonio
Toldo, Stefano
author_sort Mezzaroma, Eleonora
collection PubMed
description Virtually all types of cardiovascular diseases are associated with pathological activation of the innate immune system. The NACHT, leucine-rich repeat (LRR), and pyrin domain (PYD)-containing protein 3 (NLRP3) inflammasome is a protein complex that functions as a platform for rapid induction of the inflammatory response to infection or sterile injury. NLRP3 is an intracellular sensor that is sensitive to danger signals, such as ischemia and extracellular or intracellular alarmins during tissue injury. The NLRP3 inflammasome is regulated by the presence of damage-associated molecular patterns and initiates or amplifies inflammatory response through the production of interleukin-1β (IL-1β) and/or IL-18. NLRP3 activation regulates cell survival through the activity of caspase-1 and gasdermin-D. The development of NLRP3 inflammasome inhibitors has opened the possibility to targeting the deleterious effects of NLRP3. Here, we examine the scientific evidence supporting a role for NLRP3 and the effects of inhibitors in cardiovascular diseases.
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spelling pubmed-79176212021-03-02 NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases Mezzaroma, Eleonora Abbate, Antonio Toldo, Stefano Molecules Review Virtually all types of cardiovascular diseases are associated with pathological activation of the innate immune system. The NACHT, leucine-rich repeat (LRR), and pyrin domain (PYD)-containing protein 3 (NLRP3) inflammasome is a protein complex that functions as a platform for rapid induction of the inflammatory response to infection or sterile injury. NLRP3 is an intracellular sensor that is sensitive to danger signals, such as ischemia and extracellular or intracellular alarmins during tissue injury. The NLRP3 inflammasome is regulated by the presence of damage-associated molecular patterns and initiates or amplifies inflammatory response through the production of interleukin-1β (IL-1β) and/or IL-18. NLRP3 activation regulates cell survival through the activity of caspase-1 and gasdermin-D. The development of NLRP3 inflammasome inhibitors has opened the possibility to targeting the deleterious effects of NLRP3. Here, we examine the scientific evidence supporting a role for NLRP3 and the effects of inhibitors in cardiovascular diseases. MDPI 2021-02-12 /pmc/articles/PMC7917621/ /pubmed/33673188 http://dx.doi.org/10.3390/molecules26040976 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mezzaroma, Eleonora
Abbate, Antonio
Toldo, Stefano
NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases
title NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases
title_full NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases
title_fullStr NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases
title_full_unstemmed NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases
title_short NLRP3 Inflammasome Inhibitors in Cardiovascular Diseases
title_sort nlrp3 inflammasome inhibitors in cardiovascular diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917621/
https://www.ncbi.nlm.nih.gov/pubmed/33673188
http://dx.doi.org/10.3390/molecules26040976
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