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Title:The role of heparan sulfate and neuropilin 2 in VEGFA signaling in human endothelial tip cells and non-tip cells during angiogenesis in vitro
Authors:ID Dallinga, Marchien G. (Author)
ID Habani, Yasmin I. (Author)
ID Schimmel, Alinda W. M. (Author)
ID Dallinga-Thie, Geesje M. (Author)
ID Noorden, Cornelis J. F. van (Author)
ID Klaassen, Ingeborg (Author)
ID Schlingemann, Reinier O. (Author)
Files:URL URL - Source URL, visit https://www.mdpi.com/2073-4409/10/4/926
 
.pdf PDF - Presentation file, download (3,24 MB)
MD5: 9D87E37BEDFE2597F561A4702DAF0767
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo NIB - National Institute of Biology
Abstract:During angiogenesis, vascular endothelial growth factor A (VEGFA) regulates endothelial cell (EC) survival, tip cell formation, and stalk cell proliferation via VEGF receptor 2 (VEGFR2). VEGFR2 can interact with VEGFR2 co-receptors such as heparan sulfate proteoglycans (HSPGs) and neuropilin 2 (NRP2), but the exact roles of these co-receptors, or of sulfatase 2 (SULF2), an enzyme that removes sulfate groups from HSPGs and inhibits HSPG-mediated uptake of very low density lipoprotein (VLDL), in angiogenesis and tip cell biology are unknown. In the present study, we investigated whether the modulation of binding of VEGFA to VEGFR2 by knockdown of SULF2 or NRP2 affects sprouting angiogenesis, tip cell formation, proliferation of non-tip cells, and EC survival, or uptake of VLDL. To this end, we employed VEGFA splice variant 121, which lacks an HSPG binding domain, and VEGFA splice variant 165, which does have this domain, in in vitro models of angiogenic tip cells and vascular sprouting. We conclude that VEGFA165 and VEGFA121 have similar inducing effects on tip cells and sprouting in vitro, and that the binding of VEGFA165 to HSPGs in the extracellular matrix does not seem to play a role, as knockdown of SULF2 did not alter these effects. Co-binding of NRP2 appears to regulate VEGFA–VEGFR2-induced sprout initiation, but not tip cell formation. Finally, as the addition of VLDL increased sprout formation but not tip cell formation, and as VLDL uptake was limited to non-tip cells, our findings suggest that VLDL plays a role in sprout formation by providing biomass for stalk cell proliferation.
Keywords:endothelial cells, angiogenesis, VEGFA, tip cells, SULF2, NRP2, HSPG
Publication status:Published
Publication version:Version of Record
Publication date:16.04.2021
Year of publishing:2021
Number of pages:str. 1-17
Numbering:Vol. 10, iss. 4
PID:20.500.12556/DiRROS-19472 New window
UDC:577.2
ISSN on article:2073-4409
DOI:10.3390/cells10040926 New window
COBISS.SI-ID:61567747 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 3. 5. 2021;
Publication date in DiRROS:19.07.2024
Views:265
Downloads:204
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Record is a part of a journal

Title:Cells
Shortened title:Cells
Publisher:MDPI
ISSN:2073-4409
COBISS.SI-ID:519958809 New window

Document is financed by a project

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:UitZicht
Project number:UitZicht2013-12 and UitZicht2018-26

Funder:Other - Other funder or multiple funders
Funding programme:Rotterdamse Stichting Blindenbelangen
Project number:B20130006, B20180072

Funder:Other - Other funder or multiple funders
Funding programme:Stichting Nederlands Oogheelkundig Onderzoek
Project number:2013-04

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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