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Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes

Different tissues have different endothelial features, however, the implications of this heterogeneity in pathological responses are not clear yet. “Inflamm-aging” has been hypothesized as a possible trigger of diseases, including osteoarthritis (OA) and sarcopenia, often present in the same patient...

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Autores principales: Arrigoni, Chiara, Ostano, Paola, Bersini, Simone, Crippa, Martina, Colombo, Maria Vittoria, Gilardi, Mara, Zagra, Luigi, Mello-Grand, Maurizia, Gregnanin, Ilaria, Ghilardi, Carmen, Bani, Maria Rosa, Candrian, Christian, Chiorino, Giovanna, Moretti, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889796/
https://www.ncbi.nlm.nih.gov/pubmed/36721025
http://dx.doi.org/10.1038/s42003-023-04515-9
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author Arrigoni, Chiara
Ostano, Paola
Bersini, Simone
Crippa, Martina
Colombo, Maria Vittoria
Gilardi, Mara
Zagra, Luigi
Mello-Grand, Maurizia
Gregnanin, Ilaria
Ghilardi, Carmen
Bani, Maria Rosa
Candrian, Christian
Chiorino, Giovanna
Moretti, Matteo
author_facet Arrigoni, Chiara
Ostano, Paola
Bersini, Simone
Crippa, Martina
Colombo, Maria Vittoria
Gilardi, Mara
Zagra, Luigi
Mello-Grand, Maurizia
Gregnanin, Ilaria
Ghilardi, Carmen
Bani, Maria Rosa
Candrian, Christian
Chiorino, Giovanna
Moretti, Matteo
author_sort Arrigoni, Chiara
collection PubMed
description Different tissues have different endothelial features, however, the implications of this heterogeneity in pathological responses are not clear yet. “Inflamm-aging” has been hypothesized as a possible trigger of diseases, including osteoarthritis (OA) and sarcopenia, often present in the same patient. To highlight a possible contribution of organ-specific endothelial cells (ECs), we compare ECs derived from bone and skeletal muscle of the same OA patients. OA bone ECs show a pro-inflammatory signature and higher angiogenic sprouting as compared to muscle ECs, in control conditions and stimulated with TNFα. Furthermore, growth of muscle but not bone ECs decreases with increasing patient age and systemic inflammation. Overall, our data demonstrate that inflammatory conditions in OA patients differently affect bone and muscle ECs, suggesting that inflammatory processes increase angiogenesis in subchondral bone while associated systemic low-grade inflammation impairs angiogenesis in muscle, possibly highlighting a vascular trigger linking OA and sarcopenia.
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spelling pubmed-98897962023-02-02 Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes Arrigoni, Chiara Ostano, Paola Bersini, Simone Crippa, Martina Colombo, Maria Vittoria Gilardi, Mara Zagra, Luigi Mello-Grand, Maurizia Gregnanin, Ilaria Ghilardi, Carmen Bani, Maria Rosa Candrian, Christian Chiorino, Giovanna Moretti, Matteo Commun Biol Article Different tissues have different endothelial features, however, the implications of this heterogeneity in pathological responses are not clear yet. “Inflamm-aging” has been hypothesized as a possible trigger of diseases, including osteoarthritis (OA) and sarcopenia, often present in the same patient. To highlight a possible contribution of organ-specific endothelial cells (ECs), we compare ECs derived from bone and skeletal muscle of the same OA patients. OA bone ECs show a pro-inflammatory signature and higher angiogenic sprouting as compared to muscle ECs, in control conditions and stimulated with TNFα. Furthermore, growth of muscle but not bone ECs decreases with increasing patient age and systemic inflammation. Overall, our data demonstrate that inflammatory conditions in OA patients differently affect bone and muscle ECs, suggesting that inflammatory processes increase angiogenesis in subchondral bone while associated systemic low-grade inflammation impairs angiogenesis in muscle, possibly highlighting a vascular trigger linking OA and sarcopenia. Nature Publishing Group UK 2023-01-31 /pmc/articles/PMC9889796/ /pubmed/36721025 http://dx.doi.org/10.1038/s42003-023-04515-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Arrigoni, Chiara
Ostano, Paola
Bersini, Simone
Crippa, Martina
Colombo, Maria Vittoria
Gilardi, Mara
Zagra, Luigi
Mello-Grand, Maurizia
Gregnanin, Ilaria
Ghilardi, Carmen
Bani, Maria Rosa
Candrian, Christian
Chiorino, Giovanna
Moretti, Matteo
Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
title Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
title_full Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
title_fullStr Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
title_full_unstemmed Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
title_short Differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
title_sort differential angiogenesis of bone and muscle endothelium in aging and inflammatory processes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889796/
https://www.ncbi.nlm.nih.gov/pubmed/36721025
http://dx.doi.org/10.1038/s42003-023-04515-9
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