Expression and localisation of thymosin beta-4 in the developing human early fetal heart.
BACKGROUND:The objective of this study was to investigate the expression and localisation of thymosin β4 (Tβ4) in the developing human heart. Tβ4 is a cardioprotective protein which may have therapeutic potential. While Tβ4 is an endogenously produced protein with known importance during development...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2018-01-01
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| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC6226193?pdf=render |
| _version_ | 1811325141458616320 |
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| author | Vinay Saunders Jennifer M Dewing Tilman Sanchez-Elsner David I Wilson |
| author_facet | Vinay Saunders Jennifer M Dewing Tilman Sanchez-Elsner David I Wilson |
| author_sort | Vinay Saunders |
| collection | DOAJ |
| description | BACKGROUND:The objective of this study was to investigate the expression and localisation of thymosin β4 (Tβ4) in the developing human heart. Tβ4 is a cardioprotective protein which may have therapeutic potential. While Tβ4 is an endogenously produced protein with known importance during development, its role within the developing human heart is not fully understood. Elucidating the localisation of Tβ4 within the developing heart will help in understanding its role during cardiac development and is crucial for understanding its potential for cardioprotection and repair in the adult heart. METHODS:Expression of Tβ4 mRNA in the early fetal human heart was assessed by PCR using both ventricular and atrial tissue. Fluorescence immunohistochemistry was used to assess the localisation of Tβ4 in sections of early fetal human heart. Co-staining with CD31, an endothelial cell marker, and with myosin heavy chain, a cardiomyocyte marker, was used to determine whether Tβ4 is localised to these cell types within the early fetal human heart. RESULTS:Tβ4 mRNA was found to be expressed in both the atria and the ventricles of the early fetal human heart. Tβ4 protein was found to be primarily localised to CD31-expressing endothelial cells and the endocardium as well as being present in the epicardium. Tβ4-associated fluorescence was greater in the compact layer of the myocardial wall and the interventricular septum than in the trabecular layer of the myocardium. CONCLUSIONS:The data presented illustrates expression of Tβ4 in the developing human heart and demonstrates for the first time that Tβ4 in the human heart is primarily localised to endothelial cells of the cardiac microvasculature and coronary vessels as-well as to the endothelial-like cells of the endocardium and to the epicardium. |
| first_indexed | 2024-04-13T14:27:53Z |
| format | Article |
| id | doaj.art-e84083b56ae745beb59c6880ed9b6771 |
| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-04-13T14:27:53Z |
| publishDate | 2018-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-e84083b56ae745beb59c6880ed9b67712022-12-22T02:43:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011311e020724810.1371/journal.pone.0207248Expression and localisation of thymosin beta-4 in the developing human early fetal heart.Vinay SaundersJennifer M DewingTilman Sanchez-ElsnerDavid I WilsonBACKGROUND:The objective of this study was to investigate the expression and localisation of thymosin β4 (Tβ4) in the developing human heart. Tβ4 is a cardioprotective protein which may have therapeutic potential. While Tβ4 is an endogenously produced protein with known importance during development, its role within the developing human heart is not fully understood. Elucidating the localisation of Tβ4 within the developing heart will help in understanding its role during cardiac development and is crucial for understanding its potential for cardioprotection and repair in the adult heart. METHODS:Expression of Tβ4 mRNA in the early fetal human heart was assessed by PCR using both ventricular and atrial tissue. Fluorescence immunohistochemistry was used to assess the localisation of Tβ4 in sections of early fetal human heart. Co-staining with CD31, an endothelial cell marker, and with myosin heavy chain, a cardiomyocyte marker, was used to determine whether Tβ4 is localised to these cell types within the early fetal human heart. RESULTS:Tβ4 mRNA was found to be expressed in both the atria and the ventricles of the early fetal human heart. Tβ4 protein was found to be primarily localised to CD31-expressing endothelial cells and the endocardium as well as being present in the epicardium. Tβ4-associated fluorescence was greater in the compact layer of the myocardial wall and the interventricular septum than in the trabecular layer of the myocardium. CONCLUSIONS:The data presented illustrates expression of Tβ4 in the developing human heart and demonstrates for the first time that Tβ4 in the human heart is primarily localised to endothelial cells of the cardiac microvasculature and coronary vessels as-well as to the endothelial-like cells of the endocardium and to the epicardium.http://europepmc.org/articles/PMC6226193?pdf=render |
| spellingShingle | Vinay Saunders Jennifer M Dewing Tilman Sanchez-Elsner David I Wilson Expression and localisation of thymosin beta-4 in the developing human early fetal heart. PLoS ONE |
| title | Expression and localisation of thymosin beta-4 in the developing human early fetal heart. |
| title_full | Expression and localisation of thymosin beta-4 in the developing human early fetal heart. |
| title_fullStr | Expression and localisation of thymosin beta-4 in the developing human early fetal heart. |
| title_full_unstemmed | Expression and localisation of thymosin beta-4 in the developing human early fetal heart. |
| title_short | Expression and localisation of thymosin beta-4 in the developing human early fetal heart. |
| title_sort | expression and localisation of thymosin beta 4 in the developing human early fetal heart |
| url | http://europepmc.org/articles/PMC6226193?pdf=render |
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