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Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis
Embryonic aortic arches (AA) are initially bilaterally paired, transitional vessels and failures in remodeling based on hemodynamic and growth-related adaptations cause a spectrum of congenital heart disease (CHD) anatomies. Identifying regulatory mechanisms and cross-talk between the genetic elemen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240117/ https://www.ncbi.nlm.nih.gov/pubmed/30446764 http://dx.doi.org/10.1038/s41598-018-35127-7 |
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author | Karakaya, Cansu Goktas, Selda Celik, Merve Kowalski, William J. Keller, Bradley B. Pekkan, Kerem |
author_facet | Karakaya, Cansu Goktas, Selda Celik, Merve Kowalski, William J. Keller, Bradley B. Pekkan, Kerem |
author_sort | Karakaya, Cansu |
collection | PubMed |
description | Embryonic aortic arches (AA) are initially bilaterally paired, transitional vessels and failures in remodeling based on hemodynamic and growth-related adaptations cause a spectrum of congenital heart disease (CHD) anatomies. Identifying regulatory mechanisms and cross-talk between the genetic elements of these vessels are critical to understand the ethiology of CHD and refine predictive computational models. This study aims to screen expression profiles of fundamental biological pathways in AA at early stages of chick embryo morphogenesis and correlate them with our current understanding of growth and mechanical loading. Reverse transcription-quantitative PCR (RT-qPCR) was followed by correlation and novel peak expression analyses to compare the behaviour and activation period of the genes. Available protein networks were also integrated to investigate the interactions between molecules and highlight major hierarchies. Only wall shear stress (WSS) and growth-correlated expression patterns were investigated. Effect of WSS was seen directly on angiogenesis as well on structural and apoptosis-related genes. Our time-resolved network suggested that WSS-correlated genes coordinate the activity of critical growth factors. Moreover, differential gene expression of left and right AA might be an indicator of subsequent asymmetric morphogenesis. These findings may further our understanding of the complex processes of cardiac morphogenesis and errors resulting in CHD. |
format | Online Article Text |
id | pubmed-6240117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62401172018-11-26 Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis Karakaya, Cansu Goktas, Selda Celik, Merve Kowalski, William J. Keller, Bradley B. Pekkan, Kerem Sci Rep Article Embryonic aortic arches (AA) are initially bilaterally paired, transitional vessels and failures in remodeling based on hemodynamic and growth-related adaptations cause a spectrum of congenital heart disease (CHD) anatomies. Identifying regulatory mechanisms and cross-talk between the genetic elements of these vessels are critical to understand the ethiology of CHD and refine predictive computational models. This study aims to screen expression profiles of fundamental biological pathways in AA at early stages of chick embryo morphogenesis and correlate them with our current understanding of growth and mechanical loading. Reverse transcription-quantitative PCR (RT-qPCR) was followed by correlation and novel peak expression analyses to compare the behaviour and activation period of the genes. Available protein networks were also integrated to investigate the interactions between molecules and highlight major hierarchies. Only wall shear stress (WSS) and growth-correlated expression patterns were investigated. Effect of WSS was seen directly on angiogenesis as well on structural and apoptosis-related genes. Our time-resolved network suggested that WSS-correlated genes coordinate the activity of critical growth factors. Moreover, differential gene expression of left and right AA might be an indicator of subsequent asymmetric morphogenesis. These findings may further our understanding of the complex processes of cardiac morphogenesis and errors resulting in CHD. Nature Publishing Group UK 2018-11-16 /pmc/articles/PMC6240117/ /pubmed/30446764 http://dx.doi.org/10.1038/s41598-018-35127-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Karakaya, Cansu Goktas, Selda Celik, Merve Kowalski, William J. Keller, Bradley B. Pekkan, Kerem Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis |
title | Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis |
title_full | Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis |
title_fullStr | Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis |
title_full_unstemmed | Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis |
title_short | Asymmetry in Mechanosensitive Gene Expression during Aortic Arch Morphogenesis |
title_sort | asymmetry in mechanosensitive gene expression during aortic arch morphogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240117/ https://www.ncbi.nlm.nih.gov/pubmed/30446764 http://dx.doi.org/10.1038/s41598-018-35127-7 |
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