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Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components
Brain arteriovenous malformation (BAVM) is an abnormality in the cerebral vascular system. Although the upregulation of the Notch signalling pathway is a deterministic factor in BAVM, the mechanism by which this pathway is upregulated in patients with BAVM is uncertain. The effects of serum starvati...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450735/ https://www.ncbi.nlm.nih.gov/pubmed/34231445 http://dx.doi.org/10.1177/00368504211028387 |
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author | Li, Liming Liu, Xiaqing Zhao, Mingguang Guo, Peng Zhang, Haifeng |
author_facet | Li, Liming Liu, Xiaqing Zhao, Mingguang Guo, Peng Zhang, Haifeng |
author_sort | Li, Liming |
collection | PubMed |
description | Brain arteriovenous malformation (BAVM) is an abnormality in the cerebral vascular system. Although the upregulation of the Notch signalling pathway is a deterministic factor in BAVM, the mechanism by which this pathway is upregulated in patients with BAVM is uncertain. The effects of serum starvation and vascular endothelial growth factor (VEGF) stimulation on the Notch signalling pathway in brain microvascular endothelial cells (MECs) and mouse embryonic stem (mES)/embryoid body (EB)-derived endothelial cells were investigated in this study. The duration of serum starvation and VEGF concentration were changed, cell viability was measured, and reasonable time and concentration gradients were selected for subsequent studies. Protein and mRNA expression levels of Notch signalling pathway components in both MECs and mES/EB-derived endothelial cells were detected using western blotting and real-time PCR, respectively. Expression levels of the Notch1, Notch4, Jagged1, delta-like ligand 4 (Dll4) and Hes1 proteins and mRNAs were upregulated by lower VEGF concentrations and shorter-term serum starvation but inhibited by higher VEGF concentrations and longer-term serum starvation. This study revealed effects of changes in the duration of serum starvation and VEGF concentration on the expression of Notch signalling pathway components in both MECs and mES/EB-derived endothelial cells, potentially contributing to BAVM formation. |
format | Online Article Text |
id | pubmed-10450735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-104507352023-08-26 Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components Li, Liming Liu, Xiaqing Zhao, Mingguang Guo, Peng Zhang, Haifeng Sci Prog Article Brain arteriovenous malformation (BAVM) is an abnormality in the cerebral vascular system. Although the upregulation of the Notch signalling pathway is a deterministic factor in BAVM, the mechanism by which this pathway is upregulated in patients with BAVM is uncertain. The effects of serum starvation and vascular endothelial growth factor (VEGF) stimulation on the Notch signalling pathway in brain microvascular endothelial cells (MECs) and mouse embryonic stem (mES)/embryoid body (EB)-derived endothelial cells were investigated in this study. The duration of serum starvation and VEGF concentration were changed, cell viability was measured, and reasonable time and concentration gradients were selected for subsequent studies. Protein and mRNA expression levels of Notch signalling pathway components in both MECs and mES/EB-derived endothelial cells were detected using western blotting and real-time PCR, respectively. Expression levels of the Notch1, Notch4, Jagged1, delta-like ligand 4 (Dll4) and Hes1 proteins and mRNAs were upregulated by lower VEGF concentrations and shorter-term serum starvation but inhibited by higher VEGF concentrations and longer-term serum starvation. This study revealed effects of changes in the duration of serum starvation and VEGF concentration on the expression of Notch signalling pathway components in both MECs and mES/EB-derived endothelial cells, potentially contributing to BAVM formation. SAGE Publications 2021-07-07 /pmc/articles/PMC10450735/ /pubmed/34231445 http://dx.doi.org/10.1177/00368504211028387 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Article Li, Liming Liu, Xiaqing Zhao, Mingguang Guo, Peng Zhang, Haifeng Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components |
title | Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components |
title_full | Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components |
title_fullStr | Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components |
title_full_unstemmed | Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components |
title_short | Effects of serum starvation and vascular endothelial growth factor stimulation on the expression of Notch signalling pathway components |
title_sort | effects of serum starvation and vascular endothelial growth factor stimulation on the expression of notch signalling pathway components |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450735/ https://www.ncbi.nlm.nih.gov/pubmed/34231445 http://dx.doi.org/10.1177/00368504211028387 |
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