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Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition

Critical limb ischemia (CLI) is a hazardous manifestation of atherosclerosis and treatment failure is common. Abnormalities in the arterioles might underlie this failure but the cellular pathobiology of microvessels in CLI is poorly understood. We analyzed 349 intramuscular arterioles in lower limb...

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Autores principales: Chevalier, Jacqueline, Yin, Hao, Arpino, John-Michael, O'Neil, Caroline, Nong, Zengxuan, Gilmore, Kevin J., Lee, Jason J., Prescott, Emma, Hewak, Matthew, Rice, Charles L., Dubois, Luc, Power, Adam H., Hamilton, Douglas W., Pickering, J. Geoffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322363/
https://www.ncbi.nlm.nih.gov/pubmed/32629616
http://dx.doi.org/10.1016/j.isci.2020.101251
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author Chevalier, Jacqueline
Yin, Hao
Arpino, John-Michael
O'Neil, Caroline
Nong, Zengxuan
Gilmore, Kevin J.
Lee, Jason J.
Prescott, Emma
Hewak, Matthew
Rice, Charles L.
Dubois, Luc
Power, Adam H.
Hamilton, Douglas W.
Pickering, J. Geoffrey
author_facet Chevalier, Jacqueline
Yin, Hao
Arpino, John-Michael
O'Neil, Caroline
Nong, Zengxuan
Gilmore, Kevin J.
Lee, Jason J.
Prescott, Emma
Hewak, Matthew
Rice, Charles L.
Dubois, Luc
Power, Adam H.
Hamilton, Douglas W.
Pickering, J. Geoffrey
author_sort Chevalier, Jacqueline
collection PubMed
description Critical limb ischemia (CLI) is a hazardous manifestation of atherosclerosis and treatment failure is common. Abnormalities in the arterioles might underlie this failure but the cellular pathobiology of microvessels in CLI is poorly understood. We analyzed 349 intramuscular arterioles in lower limb specimens from individuals with and without CLI. Arteriolar densities were 1.8-fold higher in CLI muscles. However, 33% of small (<20 μm) arterioles were stenotic and 9% were completely occluded. The lumens were closed by bulky, re-oriented endothelial cells expressing abundant N-cadherin that uniquely localized between adjacent and opposing endothelial cells. S100A4 and SNAIL1 were also expressed, supporting an endothelial-to-mesenchymal transition. SMAD2/3 was activated in occlusive endothelial cells and TGFβ1 was increased in the adjacent mural cells. These findings identify a microvascular closure process based on mesenchymal transitions in a hyper-TGFß environment that may, in part, explain the limited success of peripheral artery revascularization procedures.
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spelling pubmed-73223632020-06-30 Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition Chevalier, Jacqueline Yin, Hao Arpino, John-Michael O'Neil, Caroline Nong, Zengxuan Gilmore, Kevin J. Lee, Jason J. Prescott, Emma Hewak, Matthew Rice, Charles L. Dubois, Luc Power, Adam H. Hamilton, Douglas W. Pickering, J. Geoffrey iScience Article Critical limb ischemia (CLI) is a hazardous manifestation of atherosclerosis and treatment failure is common. Abnormalities in the arterioles might underlie this failure but the cellular pathobiology of microvessels in CLI is poorly understood. We analyzed 349 intramuscular arterioles in lower limb specimens from individuals with and without CLI. Arteriolar densities were 1.8-fold higher in CLI muscles. However, 33% of small (<20 μm) arterioles were stenotic and 9% were completely occluded. The lumens were closed by bulky, re-oriented endothelial cells expressing abundant N-cadherin that uniquely localized between adjacent and opposing endothelial cells. S100A4 and SNAIL1 were also expressed, supporting an endothelial-to-mesenchymal transition. SMAD2/3 was activated in occlusive endothelial cells and TGFβ1 was increased in the adjacent mural cells. These findings identify a microvascular closure process based on mesenchymal transitions in a hyper-TGFß environment that may, in part, explain the limited success of peripheral artery revascularization procedures. Elsevier 2020-06-06 /pmc/articles/PMC7322363/ /pubmed/32629616 http://dx.doi.org/10.1016/j.isci.2020.101251 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Chevalier, Jacqueline
Yin, Hao
Arpino, John-Michael
O'Neil, Caroline
Nong, Zengxuan
Gilmore, Kevin J.
Lee, Jason J.
Prescott, Emma
Hewak, Matthew
Rice, Charles L.
Dubois, Luc
Power, Adam H.
Hamilton, Douglas W.
Pickering, J. Geoffrey
Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition
title Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition
title_full Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition
title_fullStr Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition
title_full_unstemmed Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition
title_short Obstruction of Small Arterioles in Patients with Critical Limb Ischemia due to Partial Endothelial-to-Mesenchymal Transition
title_sort obstruction of small arterioles in patients with critical limb ischemia due to partial endothelial-to-mesenchymal transition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322363/
https://www.ncbi.nlm.nih.gov/pubmed/32629616
http://dx.doi.org/10.1016/j.isci.2020.101251
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