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Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening

Angiogenesis in arterial intimal thickening (AIT) has been considered mainly in late AIT stages and only refers to sprouting angiogenesis. We assess angiogenesis during early AIT development and the occurrence of the intussusceptive type. For this purpose, we studied AIT development in (a) human art...

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Autores principales: Díaz-Flores, Lucio, Gutiérrez, Ricardo, García, Mª Pino, Gayoso, Sara, Carrasco, José Luís, Díaz-Flores, Lucio., González-Gómez, Miriam, Madrid, Juan Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663623/
https://www.ncbi.nlm.nih.gov/pubmed/33126763
http://dx.doi.org/10.3390/ijms21218049
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author Díaz-Flores, Lucio
Gutiérrez, Ricardo
García, Mª Pino
Gayoso, Sara
Carrasco, José Luís
Díaz-Flores, Lucio.
González-Gómez, Miriam
Madrid, Juan Francisco
author_facet Díaz-Flores, Lucio
Gutiérrez, Ricardo
García, Mª Pino
Gayoso, Sara
Carrasco, José Luís
Díaz-Flores, Lucio.
González-Gómez, Miriam
Madrid, Juan Francisco
author_sort Díaz-Flores, Lucio
collection PubMed
description Angiogenesis in arterial intimal thickening (AIT) has been considered mainly in late AIT stages and only refers to sprouting angiogenesis. We assess angiogenesis during early AIT development and the occurrence of the intussusceptive type. For this purpose, we studied AIT development in (a) human arteries with vasculitis in gallbladders with acute cholecystitis and urgent (n = 25) or delayed (n = 20) cholecystectomy, using immunohistochemical techniques and (b) experimentally occluded arterial segments (n = 56), using semithin and ultrathin sections and electron microscopy. The results showed transitory angiogenic phenomena, with formation of an important microvasculature, followed by vessel regression. In addition to the sequential description of angiogenic and regressive findings, we mainly contribute (a) formation of intravascular pillars (hallmarks of intussusception) during angiogenesis and vessel regression and (b) morphological interrelation between endothelial cells (ECs) in the arterial wall and vascular smooth muscle cells (VSMCs), which adopt a pericytic arrangement and establish peg-and-socket junctions with ECs. In conclusion, angiogenesis and vessel regression play an important role in AIT development in the conditions studied, with participation of intussusceptive angiogenesis during the formation and regression of a provisional microvasculature and with morphologic interrelation between ECs and VSMCs.
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spelling pubmed-76636232020-11-14 Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening Díaz-Flores, Lucio Gutiérrez, Ricardo García, Mª Pino Gayoso, Sara Carrasco, José Luís Díaz-Flores, Lucio. González-Gómez, Miriam Madrid, Juan Francisco Int J Mol Sci Article Angiogenesis in arterial intimal thickening (AIT) has been considered mainly in late AIT stages and only refers to sprouting angiogenesis. We assess angiogenesis during early AIT development and the occurrence of the intussusceptive type. For this purpose, we studied AIT development in (a) human arteries with vasculitis in gallbladders with acute cholecystitis and urgent (n = 25) or delayed (n = 20) cholecystectomy, using immunohistochemical techniques and (b) experimentally occluded arterial segments (n = 56), using semithin and ultrathin sections and electron microscopy. The results showed transitory angiogenic phenomena, with formation of an important microvasculature, followed by vessel regression. In addition to the sequential description of angiogenic and regressive findings, we mainly contribute (a) formation of intravascular pillars (hallmarks of intussusception) during angiogenesis and vessel regression and (b) morphological interrelation between endothelial cells (ECs) in the arterial wall and vascular smooth muscle cells (VSMCs), which adopt a pericytic arrangement and establish peg-and-socket junctions with ECs. In conclusion, angiogenesis and vessel regression play an important role in AIT development in the conditions studied, with participation of intussusceptive angiogenesis during the formation and regression of a provisional microvasculature and with morphologic interrelation between ECs and VSMCs. MDPI 2020-10-28 /pmc/articles/PMC7663623/ /pubmed/33126763 http://dx.doi.org/10.3390/ijms21218049 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
Díaz-Flores, Lucio
Gutiérrez, Ricardo
García, Mª Pino
Gayoso, Sara
Carrasco, José Luís
Díaz-Flores, Lucio.
González-Gómez, Miriam
Madrid, Juan Francisco
Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening
title Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening
title_full Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening
title_fullStr Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening
title_full_unstemmed Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening
title_short Intussusceptive Angiogenesis and Peg–Socket Junctions between Endothelial Cells and Smooth Muscle Cells in Early Arterial Intimal Thickening
title_sort intussusceptive angiogenesis and peg–socket junctions between endothelial cells and smooth muscle cells in early arterial intimal thickening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663623/
https://www.ncbi.nlm.nih.gov/pubmed/33126763
http://dx.doi.org/10.3390/ijms21218049
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