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Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells
Hutchinson–Gilford progeria syndrome (HGPS) is a rare premature aging disorder notably characterized by precocious and deadly atherosclerosis. Almost 90% of HGPS patients carry a LMNA p.G608G splice variant that leads to the expression of a permanently farnesylated abnormal form of prelamin-A, refer...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290406/ https://www.ncbi.nlm.nih.gov/pubmed/32408587 http://dx.doi.org/10.3390/cells9051201 |
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author | Bidault, Guillaume Garcia, Marie Capeau, Jacqueline Morichon, Romain Vigouroux, Corinne Béréziat, Véronique |
author_facet | Bidault, Guillaume Garcia, Marie Capeau, Jacqueline Morichon, Romain Vigouroux, Corinne Béréziat, Véronique |
author_sort | Bidault, Guillaume |
collection | PubMed |
description | Hutchinson–Gilford progeria syndrome (HGPS) is a rare premature aging disorder notably characterized by precocious and deadly atherosclerosis. Almost 90% of HGPS patients carry a LMNA p.G608G splice variant that leads to the expression of a permanently farnesylated abnormal form of prelamin-A, referred to as progerin. Endothelial dysfunction is a key determinant of atherosclerosis, notably during aging. Previous studies have shown that progerin accumulates in HGPS patients’ endothelial cells but also during vascular physiological aging. However, whether progerin expression in human endothelial cells can recapitulate features of endothelial dysfunction is currently unknown. Herein, we evaluated the direct impact of exogenously expressed progerin and wild-type lamin-A on human endothelial cell function and senescence. Our data demonstrate that progerin, but not wild-type lamin-A, overexpression induces endothelial cell dysfunction, characterized by increased inflammation and oxidative stress together with persistent DNA damage, increased cell cycle arrest protein expression and cellular senescence. Inhibition of progerin prenylation using a pravastatin–zoledronate combination partly prevents these defects. Our data suggest a direct proatherogenic role of progerin in human endothelial cells, which could contribute to HGPS-associated early atherosclerosis and also potentially be involved in physiological endothelial aging participating to age-related cardiometabolic diseases. |
format | Online Article Text |
id | pubmed-7290406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72904062020-06-15 Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells Bidault, Guillaume Garcia, Marie Capeau, Jacqueline Morichon, Romain Vigouroux, Corinne Béréziat, Véronique Cells Article Hutchinson–Gilford progeria syndrome (HGPS) is a rare premature aging disorder notably characterized by precocious and deadly atherosclerosis. Almost 90% of HGPS patients carry a LMNA p.G608G splice variant that leads to the expression of a permanently farnesylated abnormal form of prelamin-A, referred to as progerin. Endothelial dysfunction is a key determinant of atherosclerosis, notably during aging. Previous studies have shown that progerin accumulates in HGPS patients’ endothelial cells but also during vascular physiological aging. However, whether progerin expression in human endothelial cells can recapitulate features of endothelial dysfunction is currently unknown. Herein, we evaluated the direct impact of exogenously expressed progerin and wild-type lamin-A on human endothelial cell function and senescence. Our data demonstrate that progerin, but not wild-type lamin-A, overexpression induces endothelial cell dysfunction, characterized by increased inflammation and oxidative stress together with persistent DNA damage, increased cell cycle arrest protein expression and cellular senescence. Inhibition of progerin prenylation using a pravastatin–zoledronate combination partly prevents these defects. Our data suggest a direct proatherogenic role of progerin in human endothelial cells, which could contribute to HGPS-associated early atherosclerosis and also potentially be involved in physiological endothelial aging participating to age-related cardiometabolic diseases. MDPI 2020-05-12 /pmc/articles/PMC7290406/ /pubmed/32408587 http://dx.doi.org/10.3390/cells9051201 Text en © 2020 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 | Article Bidault, Guillaume Garcia, Marie Capeau, Jacqueline Morichon, Romain Vigouroux, Corinne Béréziat, Véronique Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells |
title | Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells |
title_full | Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells |
title_fullStr | Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells |
title_full_unstemmed | Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells |
title_short | Progerin Expression Induces Inflammation, Oxidative Stress and Senescence in Human Coronary Endothelial Cells |
title_sort | progerin expression induces inflammation, oxidative stress and senescence in human coronary endothelial cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290406/ https://www.ncbi.nlm.nih.gov/pubmed/32408587 http://dx.doi.org/10.3390/cells9051201 |
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