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Survey of the extracellular matrix architecture across the rat arterial tree

OBJECTIVE: To understand arterial remodeling and the pathophysiology of arterial diseases, it is necessary to understand the baseline qualities and variations in arterial structure. Arteries could differ in wall thickness, laminar structure, and laminar fenestration depending on their position withi...

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Autores principales: McCreary, Dylan D., Skirtich, Nolan F., Andraska, Elizabeth A., Tzeng, Edith, McEnaney, Ryan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739875/
https://www.ncbi.nlm.nih.gov/pubmed/35028599
http://dx.doi.org/10.1016/j.jvssci.2021.08.001
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author McCreary, Dylan D.
Skirtich, Nolan F.
Andraska, Elizabeth A.
Tzeng, Edith
McEnaney, Ryan M.
author_facet McCreary, Dylan D.
Skirtich, Nolan F.
Andraska, Elizabeth A.
Tzeng, Edith
McEnaney, Ryan M.
author_sort McCreary, Dylan D.
collection PubMed
description OBJECTIVE: To understand arterial remodeling and the pathophysiology of arterial diseases, it is necessary to understand the baseline qualities and variations in arterial structure. Arteries could differ in wall thickness, laminar structure, and laminar fenestration depending on their position within the arterial tree. We endeavored to evaluate and compare the extracellular matrix structure of different arteries throughout the arterial tree, from the aorta to the adductor muscle arteriole, with a particular focus on the internal elastic lamina (IEL). METHODS: Arterial segments were harvested from male Sprague-Dawley rats and imaged using multiple modalities. En face scans by multiphoton microscopy were used to compare native-state adventitial collagen undulation and IEL fenestration. RESULTS: Collagen undulation was similar across most examined arteries but straighter in the skeletal muscle arterioles (P < .05). The elastic lamellae showed several differences. The IEL fenestrae were similar in average size among abdominal aorta and celiac, renal, common iliac, and common femoral arteries (range, 14-24 μm(2)), with wide within-vessel variance (square of the standard deviation, 462-1904 μm(4)). However, they tended to be smaller (9.08 μm(2)) and less variable (square of the standard deviation, 88.3 μm(4)) in the popliteal artery. Fenestrae were greater in number in the superior mesenteric artery (SMA; 6686/mm(2); P < .05) and profunda femoris artery (PFA; 11,042/mm(2); P < .05) compared with the other examined vessels, which ranged in surface density from 3143/mm(2) to 4362/mm(2). The SMA and PFA also showed greater total fenestration as a proportion of the IEL surface area (SMA, 15.04%; P < .05; PFA, 24.11%; P < .001) than the other examined arteries (range of means, 4.7%-9.4%). The arteriolar IEL was structurally distinct, comparable to a low-density wireframe. Other structural differences were also noted, including differences in the number of medial lamellae along the arterial tree. CONCLUSIONS: We found that vessels at different locations along the arterial tree differ in structure. The SMA, PFA, and intramuscular arterioles have fundamental differences in the extracellular matrix structure compared with other arteries. Location-specific features such as the medial lamellae number and elastic laminar structure might have relevance to physiology and confer vulnerabilities to the development of pathology.
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spelling pubmed-87398752022-01-12 Survey of the extracellular matrix architecture across the rat arterial tree McCreary, Dylan D. Skirtich, Nolan F. Andraska, Elizabeth A. Tzeng, Edith McEnaney, Ryan M. JVS Vasc Sci Article OBJECTIVE: To understand arterial remodeling and the pathophysiology of arterial diseases, it is necessary to understand the baseline qualities and variations in arterial structure. Arteries could differ in wall thickness, laminar structure, and laminar fenestration depending on their position within the arterial tree. We endeavored to evaluate and compare the extracellular matrix structure of different arteries throughout the arterial tree, from the aorta to the adductor muscle arteriole, with a particular focus on the internal elastic lamina (IEL). METHODS: Arterial segments were harvested from male Sprague-Dawley rats and imaged using multiple modalities. En face scans by multiphoton microscopy were used to compare native-state adventitial collagen undulation and IEL fenestration. RESULTS: Collagen undulation was similar across most examined arteries but straighter in the skeletal muscle arterioles (P < .05). The elastic lamellae showed several differences. The IEL fenestrae were similar in average size among abdominal aorta and celiac, renal, common iliac, and common femoral arteries (range, 14-24 μm(2)), with wide within-vessel variance (square of the standard deviation, 462-1904 μm(4)). However, they tended to be smaller (9.08 μm(2)) and less variable (square of the standard deviation, 88.3 μm(4)) in the popliteal artery. Fenestrae were greater in number in the superior mesenteric artery (SMA; 6686/mm(2); P < .05) and profunda femoris artery (PFA; 11,042/mm(2); P < .05) compared with the other examined vessels, which ranged in surface density from 3143/mm(2) to 4362/mm(2). The SMA and PFA also showed greater total fenestration as a proportion of the IEL surface area (SMA, 15.04%; P < .05; PFA, 24.11%; P < .001) than the other examined arteries (range of means, 4.7%-9.4%). The arteriolar IEL was structurally distinct, comparable to a low-density wireframe. Other structural differences were also noted, including differences in the number of medial lamellae along the arterial tree. CONCLUSIONS: We found that vessels at different locations along the arterial tree differ in structure. The SMA, PFA, and intramuscular arterioles have fundamental differences in the extracellular matrix structure compared with other arteries. Location-specific features such as the medial lamellae number and elastic laminar structure might have relevance to physiology and confer vulnerabilities to the development of pathology. Elsevier 2021-08-28 /pmc/articles/PMC8739875/ /pubmed/35028599 http://dx.doi.org/10.1016/j.jvssci.2021.08.001 Text en © 2021 by the Society for Vascular Surgery. Published by Elsevier Inc. https://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
McCreary, Dylan D.
Skirtich, Nolan F.
Andraska, Elizabeth A.
Tzeng, Edith
McEnaney, Ryan M.
Survey of the extracellular matrix architecture across the rat arterial tree
title Survey of the extracellular matrix architecture across the rat arterial tree
title_full Survey of the extracellular matrix architecture across the rat arterial tree
title_fullStr Survey of the extracellular matrix architecture across the rat arterial tree
title_full_unstemmed Survey of the extracellular matrix architecture across the rat arterial tree
title_short Survey of the extracellular matrix architecture across the rat arterial tree
title_sort survey of the extracellular matrix architecture across the rat arterial tree
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739875/
https://www.ncbi.nlm.nih.gov/pubmed/35028599
http://dx.doi.org/10.1016/j.jvssci.2021.08.001
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