dc.contributor.author
Luong, Trang T. D.
dc.contributor.author
Schelski, Nadeshda
dc.contributor.author
Boehme, Beate
dc.contributor.author
Makridakis, Manousos
dc.contributor.author
Vlahou, Antonia
dc.contributor.author
Lang, Florian
dc.contributor.author
Pieske, Burkert
dc.contributor.author
Alesutan, Ioana
dc.contributor.author
Voelkl, Jakob
dc.date.accessioned
2019-04-23T13:40:40Z
dc.date.available
2019-04-23T13:40:40Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/24481
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-2252
dc.description.abstract
Background/Aims: Fibulin-3, an extracellular matrix glycoprotein, inhibits vascular oxidative stress and remodeling in hypertension. Oxidative stress is prevalent in chronic kidney disease (CKD) patients and is an important mediator of osteo-/chondrogenic transdifferentiation and calcification of vascular smooth muscle cells (VSMCs) during hyperphosphatemia. Therefore, the present study explored the effects of Fibulin-3 on phosphate-induced vascular calcification. Methods: Experiments were performed in primary human aortic smooth muscle cells (HAoSMCs) treated with control or with phosphate without or with additional treatment with recombinant human Fibulin-3 protein or with hydrogen peroxide as an exogenous source of oxidative stress. Results: Treatment with calcification medium significantly increased calcium deposition in HAoSMCs, an effect significantly blunted by additional treatment with Fibulin-3. Moreover, phosphate-induced alkaline phosphatase activity and mRNA expression of osteogenic and chondrogenic markers MSX2, CBFA1, SOX9 and ALPL were all significantly reduced by addition of Fibulin-3. These effects were paralleled by similar regulation of oxidative stress in HAoSMCs. Phosphate treatment significantly up-regulated mRNA expression of the oxidative stress markers NOX4 and CYBA, down-regulated total antioxidant capacity and increased the expression of downstream effectors of oxidative stress PA1-1. MMP2 and MMP9 as well as BAX/BLC2 ratio in HAoSMCs, all effects blocked by additional treatment with Fibulin-3. Furthermore, the protective effects of Fibulin-3 on phosphate-induced osteogenic and chondrogenic markers expression in HAoSMCs were reversed by additional treatment with hydrogen peroxide. Conclusions: Fibulin-3 attenuates phosphate-induced osteo-/chondrogenic transdifferentiation and calcification of VSMCs, effects involving inhibition of oxidative stress. Up-regulation or supplementation of Fibulin-3 may be beneficial in reducing the progression of vascular calcification during hyperphosphatemic conditions such as CKD. (C) 2018 The Author(s) Published by S. Karger AG, Basel.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Oxidative stress
en
dc.subject
Vascular calcification
en
dc.subject
Osteo-/chondrogenic signaling
en
dc.subject
Vascular smooth muscle cells
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Fibulin-3 Attenuates Phosphate-Induced Vascular Smooth Muscle Cell Calcification by Inhibition of Oxidative Stress
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1159/000489144
dcterms.bibliographicCitation.journaltitle
Cellular Physiology and Biochemistry
dcterms.bibliographicCitation.number
4
dcterms.bibliographicCitation.originalpublishername
Karger Publishers
dcterms.bibliographicCitation.pagestart
1305
dcterms.bibliographicCitation.pageend
1316
dcterms.bibliographicCitation.volume
46
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
29689558
dcterms.isPartOf.issn
1015-8987