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Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis
We used rat experimental myocardial infarction to study the ultrastructural recovery, especially neo-angiogenesis in the infarction border zone. We were interested in the possible role(s) of telocytes (TCs), a novel type of interstitial cell very recently discovered in myocardim (see http://www.telo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822940/ https://www.ncbi.nlm.nih.gov/pubmed/21895968 http://dx.doi.org/10.1111/j.1582-4934.2011.01449.x |
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author | Manole, C G Cismaşiu, V Gherghiceanu, Mihaela Popescu, L M |
author_facet | Manole, C G Cismaşiu, V Gherghiceanu, Mihaela Popescu, L M |
author_sort | Manole, C G |
collection | PubMed |
description | We used rat experimental myocardial infarction to study the ultrastructural recovery, especially neo-angiogenesis in the infarction border zone. We were interested in the possible role(s) of telocytes (TCs), a novel type of interstitial cell very recently discovered in myocardim (see http://www.telocytes.com). Electron microscopy, immunocytochemistry and analysis of several proangiogenic microRNAs provided evidence for TC involvement in neo-angiogenesis after myocardial infarction. Electron microscopy showed the close spatial association of TCs with neoangiogenetic elements. Higher resolution images provided the following information: (a) the intercellular space between the abluminal face of endothelium and its surrounding TCs is frequently less than 50 nm; (b) TCs establish multiple direct nanocontacts with endothelial cells, where the extracellular space seems obliterated; such nanocontacts have a length of 0.4–1.5 μm; (c) the absence of basal membrane on the abluminal face of endothelial cell. Besides the physical contacts (either nanoscopic or microscopic) TCs presumably contribute to neo-angiognesis via paracrine secretion (as shown by immunocytochemistry for VEGF or NOS2). Last but not least, TCs contain measurable quantities of angiogenic microRNAs (e.g. let-7e, 10a, 21, 27b, 100, 126-3p, 130a, 143, 155, 503). Taken together, the direct (physical) contact of TCs with endothelial tubes, as well as the indirect (chemical) positive influence within the ‘angiogenic zones’, suggests an important participation of TCs in neo-angiogenesis during the late stage of myocardial infarction. |
format | Online Article Text |
id | pubmed-3822940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38229402015-04-06 Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis Manole, C G Cismaşiu, V Gherghiceanu, Mihaela Popescu, L M J Cell Mol Med Images in Cellular, Molecular Medicine We used rat experimental myocardial infarction to study the ultrastructural recovery, especially neo-angiogenesis in the infarction border zone. We were interested in the possible role(s) of telocytes (TCs), a novel type of interstitial cell very recently discovered in myocardim (see http://www.telocytes.com). Electron microscopy, immunocytochemistry and analysis of several proangiogenic microRNAs provided evidence for TC involvement in neo-angiogenesis after myocardial infarction. Electron microscopy showed the close spatial association of TCs with neoangiogenetic elements. Higher resolution images provided the following information: (a) the intercellular space between the abluminal face of endothelium and its surrounding TCs is frequently less than 50 nm; (b) TCs establish multiple direct nanocontacts with endothelial cells, where the extracellular space seems obliterated; such nanocontacts have a length of 0.4–1.5 μm; (c) the absence of basal membrane on the abluminal face of endothelial cell. Besides the physical contacts (either nanoscopic or microscopic) TCs presumably contribute to neo-angiognesis via paracrine secretion (as shown by immunocytochemistry for VEGF or NOS2). Last but not least, TCs contain measurable quantities of angiogenic microRNAs (e.g. let-7e, 10a, 21, 27b, 100, 126-3p, 130a, 143, 155, 503). Taken together, the direct (physical) contact of TCs with endothelial tubes, as well as the indirect (chemical) positive influence within the ‘angiogenic zones’, suggests an important participation of TCs in neo-angiogenesis during the late stage of myocardial infarction. Blackwell Publishing Ltd 2011-11 2011-10-24 /pmc/articles/PMC3822940/ /pubmed/21895968 http://dx.doi.org/10.1111/j.1582-4934.2011.01449.x Text en © 2011 The Authors Journal of Cellular and Molecular Medicine © 2011 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd |
spellingShingle | Images in Cellular, Molecular Medicine Manole, C G Cismaşiu, V Gherghiceanu, Mihaela Popescu, L M Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
title | Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
title_full | Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
title_fullStr | Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
title_full_unstemmed | Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
title_short | Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
title_sort | experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis |
topic | Images in Cellular, Molecular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822940/ https://www.ncbi.nlm.nih.gov/pubmed/21895968 http://dx.doi.org/10.1111/j.1582-4934.2011.01449.x |
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