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Notch1 activates angiogenic regulator Netrin4 in endothelial cells
Netrin4 (NTN4) is a chemotropic factor that regulates angiogenesis. We found that endothelial expression of the activated, intracellular domain of Notch1 (NICD1), significantly up‐regulated NTN4 mRNA as well as intracellular NTN4 protein in both transgenic mice and cultured human umbilical vein endo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484422/ https://www.ncbi.nlm.nih.gov/pubmed/30784178 http://dx.doi.org/10.1111/jcmm.14240 |
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author | Liu, Qiang Allen, Thaddeus D. Song, Wei Wada, Youichiro Lobe, Corrinne G. Liu, Ju |
author_facet | Liu, Qiang Allen, Thaddeus D. Song, Wei Wada, Youichiro Lobe, Corrinne G. Liu, Ju |
author_sort | Liu, Qiang |
collection | PubMed |
description | Netrin4 (NTN4) is a chemotropic factor that regulates angiogenesis. We found that endothelial expression of the activated, intracellular domain of Notch1 (NICD1), significantly up‐regulated NTN4 mRNA as well as intracellular NTN4 protein in both transgenic mice and cultured human umbilical vein endothelial cells (HUVECs). Notch1 activation also increased NTN4 secretion from HUVECs. We subsequently demonstrated that NICD1 bound to CSL (CBF1, Suppressor of Hairless, Lag‐1), a core component of Notch transcription complex, at the −53 element of the human NTN4 gene promoter. Loss of the −53 element compromised NICD1‐induced NTN4 expression. Our results suggest a conserved role for Notch signalling in transcriptional regulation of endothelial NTN4. |
format | Online Article Text |
id | pubmed-6484422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64844222019-05-03 Notch1 activates angiogenic regulator Netrin4 in endothelial cells Liu, Qiang Allen, Thaddeus D. Song, Wei Wada, Youichiro Lobe, Corrinne G. Liu, Ju J Cell Mol Med Short Communications Netrin4 (NTN4) is a chemotropic factor that regulates angiogenesis. We found that endothelial expression of the activated, intracellular domain of Notch1 (NICD1), significantly up‐regulated NTN4 mRNA as well as intracellular NTN4 protein in both transgenic mice and cultured human umbilical vein endothelial cells (HUVECs). Notch1 activation also increased NTN4 secretion from HUVECs. We subsequently demonstrated that NICD1 bound to CSL (CBF1, Suppressor of Hairless, Lag‐1), a core component of Notch transcription complex, at the −53 element of the human NTN4 gene promoter. Loss of the −53 element compromised NICD1‐induced NTN4 expression. Our results suggest a conserved role for Notch signalling in transcriptional regulation of endothelial NTN4. John Wiley and Sons Inc. 2019-02-19 2019-05 /pmc/articles/PMC6484422/ /pubmed/30784178 http://dx.doi.org/10.1111/jcmm.14240 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communications Liu, Qiang Allen, Thaddeus D. Song, Wei Wada, Youichiro Lobe, Corrinne G. Liu, Ju Notch1 activates angiogenic regulator Netrin4 in endothelial cells |
title | Notch1 activates angiogenic regulator Netrin4 in endothelial cells |
title_full | Notch1 activates angiogenic regulator Netrin4 in endothelial cells |
title_fullStr | Notch1 activates angiogenic regulator Netrin4 in endothelial cells |
title_full_unstemmed | Notch1 activates angiogenic regulator Netrin4 in endothelial cells |
title_short | Notch1 activates angiogenic regulator Netrin4 in endothelial cells |
title_sort | notch1 activates angiogenic regulator netrin4 in endothelial cells |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484422/ https://www.ncbi.nlm.nih.gov/pubmed/30784178 http://dx.doi.org/10.1111/jcmm.14240 |
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