Please use this identifier to cite or link to this item:
Title: Monocyte adhesion to atherosclerotic matrix proteins is enhanced by Asn-Gly-Arg deamidation
Authors: Dutta B.
Park J.E.
Kumar S.
Hao P.
Gallart-Palau X.
Serra A.
Ren Y.
Sorokin V. 
Lee C.N. 
Ho H.H.
De Kleijn D.
Sze S.K.
Issue Date: 18-Jul-2017
Publisher: Nature Publishing Group
Citation: Dutta B., Park J.E., Kumar S., Hao P., Gallart-Palau X., Serra A., Ren Y., Sorokin V., Lee C.N., Ho H.H., De Kleijn D., Sze S.K. (2017-07-18). Monocyte adhesion to atherosclerotic matrix proteins is enhanced by Asn-Gly-Arg deamidation. Scientific Reports 7 (1) : 5765. ScholarBank@NUS Repository.
Abstract: Atherosclerosis arises from leukocyte infiltration and thickening of the artery walls and constitutes a major component of vascular disease pathology, but the molecular events underpinning this process are not fully understood. Proteins containing an Asn-Gly-Arg (NGR) motif readily undergo deamidation of asparagine to generate isoDGR structures that bind to integrin ?v?3 on circulating leukocytes. Here we report the identification of isoDGR motifs in human atherosclerotic plaque components including extracellular matrix (ECM) proteins fibronectin and tenascin C, which have been strongly implicated in human atherosclerosis. We further demonstrate that deamidation of NGR motifs in fibronectin and tenascin C leads to increased adhesion of the monocytic cell line U937 and enhanced binding of primary human monocytes, except in the presence of a ?v?3-blocking antibody or the ?v-selective inhibitor cilengitide. In contrast, under the same deamidating conditions monocyte-macrophages displayed only weak binding to the alternative ECM component vitronectin which lacks NGR motifs. Together, these findings confirm a critical role for isoDGR motifs in mediating leukocyte adhesion to the ECM via integrin ?v?3 and suggest that protein deamidation may promote the pathological progression of human atherosclerosis by enhancing monocyte recruitment to developing plaques. � 2017 The Author(s).
Source Title: Scientific Reports
ISSN: 20452322
DOI: 10.1038/s41598-017-06202-2
Appears in Collections:Elements
Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
s41598-017-06202-2.pdf3.18 MBAdobe PDF




checked on Oct 20, 2019


checked on Jul 25, 2019

Page view(s)

checked on Oct 17, 2019


checked on Oct 17, 2019

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.