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Title:Diferential roles of eNOS in late efects ofVEGF‑A on hyperpermeability in diferent types of endothelial cells
Authors:ID Bosma, Esmeralda K. (Author)
ID Darwesh, Shahan (Author)
ID Habani, Yasmin I. (Author)
ID Cammeraat, Maxime (Author)
ID Serrano Martinez, Paola (Author)
ID Breest Smallenburg, Mathilda E. van (Author)
ID Zheng, JiaY. (Author)
ID Vogels, Ilse M.C. (Author)
ID Noorden, Cornelis J. F. van (Author)
ID Schlingemann, Reinier O. (Author)
ID Klaassen, Ingeborg (Author)
Files:URL URL - Source URL, visit https://www.nature.com/articles/s41598-023-46893-4
 
.pdf PDF - Presentation file, download (1,53 MB)
MD5: 375950014779F2316D27DAFE3DA1F1C6
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Abstract:Vascular endothelial growth factor (VEGF)-A induces endothelial hyperpermeability, but the molecular pathways remain incompletely understood. Endothelial nitric oxide synthase (eNOS) regulates acute efects of VEGF-A on permeability of endothelial cells (ECs), but it remains unknown whether and how eNOS regulates late efects of VEGF-A-induced hyperpermeability. Here we show that VEGF-A induces hyperpermeability via eNOS-dependent and eNOS-independent mechanisms at 2 days after VEGF-A stimulation. Silencing of expression of the eNOS gene (NOS3) reduced VEGF-A-induced permeability for dextran (70 kDa) and 766 Da-tracer in human dermal microvascular ECs (HDMVECs), but not in human retinal microvascular ECs (HRECs) and human umbilical vein ECs (HUVECs). However, silencing of NOS3 expression in HRECs increased permeability to dextran, BSA and 766 Da-tracer in the absence of VEGF-A stimulation, suggesting a barrier-protective function of eNOS. We also investigated how silencing of NOS3 expression regulates the expression of permeability-related transcripts, and found that NOS3 silencing downregulates the expression of PLVAP, a molecule associated with trans-endothelial transport via caveolae, in HDMVECs and HUVECs, but not in HRECs. Our fndings underscore the complexity of VEGF-A-induced permeability pathways in ECs and the role of eNOS therein, and demonstrate that diferent pathways are activated depending on the EC phenotype.
Keywords:endocytosis, RNAi, hyperpermeability
Publication status:Published
Publication version:Version of Record
Publication date:05.12.2023
Year of publishing:2023
Number of pages:str. 1-14
Numbering:Vol. 13, [article no.] 21436
PID:20.500.12556/DiRROS-19306 New window
UDC:577.2
ISSN on article:2045-2322
COBISS.SI-ID:190987779 New window
Note:Soavtorji: Shahan Darwesh, Yasmin I. Habani, Maxime Cammeraat, Paola Serrano Martinez, Mathilda E. van Breest Smallenburg, JiaY. Zheng , Ilse M. C.Vogels , Cornelis J. F. van Noorden, Reinier O. Schlingemann1 & Ingeborg Klaassen; Nasl. z nasl. zaslona; Opis vira z dne 31. 3. 2024;
Publication date in DiRROS:15.07.2024
Views:153
Downloads:116
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Record is a part of a journal

Title:Scientific reports
Shortened title:Sci. rep.
Publisher:Nature Publishing Group
ISSN:2045-2322
COBISS.SI-ID:18727432 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0245-2019
Name:Ekotoksiologija, toksikološka genomika in karcinogeneza

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-2526-2020
Name:Razkrivanje niše matičnih glioma celic v iskanju novih terapevtskih ciljev pri bolnikih z glioblastomom

Funder:Other - Other funder or multiple funders
Funding programme:EFSD/Boehringer Ingelheim European Research Programme in Microvascular Complications of Diabetes 2018
Project number:BI18_4

Funder:Other - Other funder or multiple funders
Funding programme:AMC Foundation

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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