Cargando…
Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro
PURPOSE: To establish a high-glucose (HG) stressed cell model and study the expression of main components of the Dll4/Notch-VEGF signaling pathway under high-glucose stimulation. METHODS: A model of HG-conditioned cells (human umbilical vein endothelial cells, HUVECs) was first established, and then...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031991/ https://www.ncbi.nlm.nih.gov/pubmed/35464260 http://dx.doi.org/10.2147/DMSO.S355004 |
_version_ | 1784692529808015360 |
---|---|
author | Gao, Na Xiao, Linghui Tao, Zheng Zheng, Yanlin Wang, Wanjie Huang, Hui |
author_facet | Gao, Na Xiao, Linghui Tao, Zheng Zheng, Yanlin Wang, Wanjie Huang, Hui |
author_sort | Gao, Na |
collection | PubMed |
description | PURPOSE: To establish a high-glucose (HG) stressed cell model and study the expression of main components of the Dll4/Notch-VEGF signaling pathway under high-glucose stimulation. METHODS: A model of HG-conditioned cells (human umbilical vein endothelial cells, HUVECs) was first established, and then the expression of Dll4, Notch1, Notch4 and VEGF in HG-stressed cells with or without Notch pathway blockage was analyzed by RT-PCR and Western blot. To observe cell migration, we also evaluated the Transwell assay. RESULTS: HUVECs stimulated with 30mmol/L HG was selected as a cell model. RT-PCR and Western blot results showed that HG stimulation induced the expression of Dll4, Notch1 and VEGF and downregulated Notch4. The expressions were reversed after Notch pathway blockage; meanwhile, the blockage of Notch pathway inhibited cell migration under HG condition. CONCLUSION: The function of Notch4 in responses to HG stimulation deserves further researching. Combination therapy by blocking Dll4/Notch and VEGF pathways may provide us with a new way for anti-neovascularization. |
format | Online Article Text |
id | pubmed-9031991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-90319912022-04-23 Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro Gao, Na Xiao, Linghui Tao, Zheng Zheng, Yanlin Wang, Wanjie Huang, Hui Diabetes Metab Syndr Obes Original Research PURPOSE: To establish a high-glucose (HG) stressed cell model and study the expression of main components of the Dll4/Notch-VEGF signaling pathway under high-glucose stimulation. METHODS: A model of HG-conditioned cells (human umbilical vein endothelial cells, HUVECs) was first established, and then the expression of Dll4, Notch1, Notch4 and VEGF in HG-stressed cells with or without Notch pathway blockage was analyzed by RT-PCR and Western blot. To observe cell migration, we also evaluated the Transwell assay. RESULTS: HUVECs stimulated with 30mmol/L HG was selected as a cell model. RT-PCR and Western blot results showed that HG stimulation induced the expression of Dll4, Notch1 and VEGF and downregulated Notch4. The expressions were reversed after Notch pathway blockage; meanwhile, the blockage of Notch pathway inhibited cell migration under HG condition. CONCLUSION: The function of Notch4 in responses to HG stimulation deserves further researching. Combination therapy by blocking Dll4/Notch and VEGF pathways may provide us with a new way for anti-neovascularization. Dove 2022-04-18 /pmc/articles/PMC9031991/ /pubmed/35464260 http://dx.doi.org/10.2147/DMSO.S355004 Text en © 2022 Gao et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Gao, Na Xiao, Linghui Tao, Zheng Zheng, Yanlin Wang, Wanjie Huang, Hui Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro |
title | Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro |
title_full | Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro |
title_fullStr | Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro |
title_full_unstemmed | Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro |
title_short | Preliminary Research of Main Components of Dll4/ Notch-VEGF Signaling Pathway Under High-Glucose Stimulation in vitro |
title_sort | preliminary research of main components of dll4/ notch-vegf signaling pathway under high-glucose stimulation in vitro |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031991/ https://www.ncbi.nlm.nih.gov/pubmed/35464260 http://dx.doi.org/10.2147/DMSO.S355004 |
work_keys_str_mv | AT gaona preliminaryresearchofmaincomponentsofdll4notchvegfsignalingpathwayunderhighglucosestimulationinvitro AT xiaolinghui preliminaryresearchofmaincomponentsofdll4notchvegfsignalingpathwayunderhighglucosestimulationinvitro AT taozheng preliminaryresearchofmaincomponentsofdll4notchvegfsignalingpathwayunderhighglucosestimulationinvitro AT zhengyanlin preliminaryresearchofmaincomponentsofdll4notchvegfsignalingpathwayunderhighglucosestimulationinvitro AT wangwanjie preliminaryresearchofmaincomponentsofdll4notchvegfsignalingpathwayunderhighglucosestimulationinvitro AT huanghui preliminaryresearchofmaincomponentsofdll4notchvegfsignalingpathwayunderhighglucosestimulationinvitro |