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Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell
This work aimed to establish the lineage of cells similar to the interstitial cells of Cajal (ICC), the arterial ICC-like (AIL) cells, which have recently been described in resistance arteries, and to study their location in the artery wall. Segments of guinea-pig mesenteric arteries and single AIL...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2121184/ https://www.ncbi.nlm.nih.gov/pubmed/17760838 http://dx.doi.org/10.1111/j.1582-4934.2007.00066.x |
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author | Pucovský, Vladimír Harhun, Maksym I Povstyan, Oleksandr V Gordienko, Dmitri V Moss, Ray F Bolton, Thomas B |
author_facet | Pucovský, Vladimír Harhun, Maksym I Povstyan, Oleksandr V Gordienko, Dmitri V Moss, Ray F Bolton, Thomas B |
author_sort | Pucovský, Vladimír |
collection | PubMed |
description | This work aimed to establish the lineage of cells similar to the interstitial cells of Cajal (ICC), the arterial ICC-like (AIL) cells, which have recently been described in resistance arteries, and to study their location in the artery wall. Segments of guinea-pig mesenteric arteries and single AIL cells freshly isolated from them were used. Confocal imaging of immunostained cells or segments and electron microscopy of artery segments were used to test for the presence and cellular localization of selected markers, and to localize AIL cells in intact artery segments. AIL cells were negative for PGP9.5, a neural marker, and for von Willebrand factor (vWF), an endothelial cell marker. They were positive for smooth muscle α-actin and smooth muscle myosin heavy chain (SM-MHC), but expressed only a small amount of smoothelin, a marker of contractile smooth muscle cells (SMC), and of myosin light chain kinase (MLCK), a critical enzyme in the regulation of smooth muscle contraction. Cell isolation in the presence of latrunculin B, an actin polymerization inhibitor, did not cause the disappearance of AIL cells from cell suspension. The fluorescence of basal lamina protein collagen IV was comparable between the AIL cells and the vascular SMCs and the fluorescence of laminin was higher in AIL cells compared to vascular SMCs. Moreover, cells with thin processes were found in the tunica media of small resistance arteries using transmis-sion electron microscopy. The results suggest that AIL cells are immature or phenotypically modulated vascular SMCs constitutively present in resistance arteries. |
format | Text |
id | pubmed-2121184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-21211842007-12-11 Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell Pucovský, Vladimír Harhun, Maksym I Povstyan, Oleksandr V Gordienko, Dmitri V Moss, Ray F Bolton, Thomas B J Cell Mol Med Articles This work aimed to establish the lineage of cells similar to the interstitial cells of Cajal (ICC), the arterial ICC-like (AIL) cells, which have recently been described in resistance arteries, and to study their location in the artery wall. Segments of guinea-pig mesenteric arteries and single AIL cells freshly isolated from them were used. Confocal imaging of immunostained cells or segments and electron microscopy of artery segments were used to test for the presence and cellular localization of selected markers, and to localize AIL cells in intact artery segments. AIL cells were negative for PGP9.5, a neural marker, and for von Willebrand factor (vWF), an endothelial cell marker. They were positive for smooth muscle α-actin and smooth muscle myosin heavy chain (SM-MHC), but expressed only a small amount of smoothelin, a marker of contractile smooth muscle cells (SMC), and of myosin light chain kinase (MLCK), a critical enzyme in the regulation of smooth muscle contraction. Cell isolation in the presence of latrunculin B, an actin polymerization inhibitor, did not cause the disappearance of AIL cells from cell suspension. The fluorescence of basal lamina protein collagen IV was comparable between the AIL cells and the vascular SMCs and the fluorescence of laminin was higher in AIL cells compared to vascular SMCs. Moreover, cells with thin processes were found in the tunica media of small resistance arteries using transmis-sion electron microscopy. The results suggest that AIL cells are immature or phenotypically modulated vascular SMCs constitutively present in resistance arteries. Blackwell Publishing Ltd 2007-07 2007-06-24 /pmc/articles/PMC2121184/ /pubmed/17760838 http://dx.doi.org/10.1111/j.1582-4934.2007.00066.x Text en © 2007 The Authors Journal compilation © 2007 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd https://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Articles Pucovský, Vladimír Harhun, Maksym I Povstyan, Oleksandr V Gordienko, Dmitri V Moss, Ray F Bolton, Thomas B Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell |
title | Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell |
title_full | Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell |
title_fullStr | Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell |
title_full_unstemmed | Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell |
title_short | Close relation of arterial ICC-like cells to the contractile phenotype of vascular smooth muscle cell |
title_sort | close relation of arterial icc-like cells to the contractile phenotype of vascular smooth muscle cell |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2121184/ https://www.ncbi.nlm.nih.gov/pubmed/17760838 http://dx.doi.org/10.1111/j.1582-4934.2007.00066.x |
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