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Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus

Vascular inflammation mediated by overly activated immune cells is a significant cause of morbidity and mortality in systemic lupus erythematosus (SLE). Several mouse models to study the pathogenesis of SLE are currently in use, many of which have different mechanisms of pathogenesis. The diversity...

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Autores principales: Ryan, Holly, Morel, Laurence, Moore, Erika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996195/
https://www.ncbi.nlm.nih.gov/pubmed/35419427
http://dx.doi.org/10.3389/fcvm.2022.767450
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author Ryan, Holly
Morel, Laurence
Moore, Erika
author_facet Ryan, Holly
Morel, Laurence
Moore, Erika
author_sort Ryan, Holly
collection PubMed
description Vascular inflammation mediated by overly activated immune cells is a significant cause of morbidity and mortality in systemic lupus erythematosus (SLE). Several mouse models to study the pathogenesis of SLE are currently in use, many of which have different mechanisms of pathogenesis. The diversity of these models allows interrogation of different aspects of the disease pathogenesis. To better determine the mechanisms by which vascular inflammation occurs in SLE, and to assist future researchers in choosing the most appropriate mouse models to study cardiovascular complications in SLE, we suggest that direct comparisons of vascular inflammation should be conducted among different murine SLE models. We also propose the use of in vitro vascular assays to further investigate vascular inflammation processes prevalent among different murine SLE models.
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spelling pubmed-89961952022-04-12 Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus Ryan, Holly Morel, Laurence Moore, Erika Front Cardiovasc Med Cardiovascular Medicine Vascular inflammation mediated by overly activated immune cells is a significant cause of morbidity and mortality in systemic lupus erythematosus (SLE). Several mouse models to study the pathogenesis of SLE are currently in use, many of which have different mechanisms of pathogenesis. The diversity of these models allows interrogation of different aspects of the disease pathogenesis. To better determine the mechanisms by which vascular inflammation occurs in SLE, and to assist future researchers in choosing the most appropriate mouse models to study cardiovascular complications in SLE, we suggest that direct comparisons of vascular inflammation should be conducted among different murine SLE models. We also propose the use of in vitro vascular assays to further investigate vascular inflammation processes prevalent among different murine SLE models. Frontiers Media S.A. 2022-03-28 /pmc/articles/PMC8996195/ /pubmed/35419427 http://dx.doi.org/10.3389/fcvm.2022.767450 Text en Copyright © 2022 Ryan, Morel and Moore. 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 Cardiovascular Medicine
Ryan, Holly
Morel, Laurence
Moore, Erika
Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus
title Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus
title_full Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus
title_fullStr Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus
title_full_unstemmed Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus
title_short Vascular Inflammation in Mouse Models of Systemic Lupus Erythematosus
title_sort vascular inflammation in mouse models of systemic lupus erythematosus
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8996195/
https://www.ncbi.nlm.nih.gov/pubmed/35419427
http://dx.doi.org/10.3389/fcvm.2022.767450
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