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Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart
BACKGROUND: Outflow tract (OFT) septation defects are a common cause of congenital heart disease. Numerous studies have focused on the septation mechanism of the OFT, but have reported inconsistent conclusions. This study, therefore, aimed to investigate the septation of the aortic sac and the OFT i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006820/ https://www.ncbi.nlm.nih.gov/pubmed/29893363 http://dx.doi.org/10.4103/0366-6999.233956 |
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author | Yang, Yan-Ping Li, Hai-Rong Cao, Xi-Mei Qiao, Cong-Jin Ya, Jing |
author_facet | Yang, Yan-Ping Li, Hai-Rong Cao, Xi-Mei Qiao, Cong-Jin Ya, Jing |
author_sort | Yang, Yan-Ping |
collection | PubMed |
description | BACKGROUND: Outflow tract (OFT) septation defects are a common cause of congenital heart disease. Numerous studies have focused on the septation mechanism of the OFT, but have reported inconsistent conclusions. This study, therefore, aimed to investigate the septation of the aortic sac and the OFT in the early embryonic human heart. METHODS: Serial sections of 27 human embryonic hearts from Carnegie stage (CS) 10 to CS19 were immunohistochemically stained with antibodies against α-smooth muscle actin (α-SMA) and myosin heavy chain. RESULTS: At CS10–CS11, the OFT wall was an exclusively myocardial structure that was continuous with the aortic sac at the margin of the pericardial cavity. From CS13 onward, the OFT was divided into nonmyocardial and myocardial portions. The cushion formed gradually, and its distal border with the OFT myocardium was consistently maintained. The aortic sac between the fourth and sixth aortic arch arteries was degenerated. At CS16, the α-SMA-positive aortopulmonary septum formed and fused with the two OFT cushions, thus septating the nonmyocardial portion of the OFT into two arteries. At this stage, the cushions were not fused. At CS19, the bilateral cushions were fused to septate the myocardial portion of the OFT. CONCLUSIONS: Data suggest that the OFT cushion is formed before the aortopulmonary septum is formed. Thus, the OFT cushion is not derived from the aortopulmonary septum. In addition, the nonmyocardial part of the OFT is septated into the aorta and pulmonary trunk by the aortopulmonary septum, while the main part of the cushion fuses and septates the myocardial portion of the OFT. |
format | Online Article Text |
id | pubmed-6006820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60068202018-06-30 Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart Yang, Yan-Ping Li, Hai-Rong Cao, Xi-Mei Qiao, Cong-Jin Ya, Jing Chin Med J (Engl) Original Article BACKGROUND: Outflow tract (OFT) septation defects are a common cause of congenital heart disease. Numerous studies have focused on the septation mechanism of the OFT, but have reported inconsistent conclusions. This study, therefore, aimed to investigate the septation of the aortic sac and the OFT in the early embryonic human heart. METHODS: Serial sections of 27 human embryonic hearts from Carnegie stage (CS) 10 to CS19 were immunohistochemically stained with antibodies against α-smooth muscle actin (α-SMA) and myosin heavy chain. RESULTS: At CS10–CS11, the OFT wall was an exclusively myocardial structure that was continuous with the aortic sac at the margin of the pericardial cavity. From CS13 onward, the OFT was divided into nonmyocardial and myocardial portions. The cushion formed gradually, and its distal border with the OFT myocardium was consistently maintained. The aortic sac between the fourth and sixth aortic arch arteries was degenerated. At CS16, the α-SMA-positive aortopulmonary septum formed and fused with the two OFT cushions, thus septating the nonmyocardial portion of the OFT into two arteries. At this stage, the cushions were not fused. At CS19, the bilateral cushions were fused to septate the myocardial portion of the OFT. CONCLUSIONS: Data suggest that the OFT cushion is formed before the aortopulmonary septum is formed. Thus, the OFT cushion is not derived from the aortopulmonary septum. In addition, the nonmyocardial part of the OFT is septated into the aorta and pulmonary trunk by the aortopulmonary septum, while the main part of the cushion fuses and septates the myocardial portion of the OFT. Medknow Publications & Media Pvt Ltd 2018-06-20 /pmc/articles/PMC6006820/ /pubmed/29893363 http://dx.doi.org/10.4103/0366-6999.233956 Text en Copyright: © 2018 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Yang, Yan-Ping Li, Hai-Rong Cao, Xi-Mei Qiao, Cong-Jin Ya, Jing Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart |
title | Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart |
title_full | Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart |
title_fullStr | Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart |
title_full_unstemmed | Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart |
title_short | Septation of the Intrapericardial Arterial Trunks in the Early Human Embryonic Heart |
title_sort | septation of the intrapericardial arterial trunks in the early human embryonic heart |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006820/ https://www.ncbi.nlm.nih.gov/pubmed/29893363 http://dx.doi.org/10.4103/0366-6999.233956 |
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