{"doi":"10.1371/journal.pone.0052209","title":"Discoidin Domain Receptors Promote α1β1- and α2β1-Integrin Mediated Cell Adhesion to Collagen by Enhancing Integrin Activation","abstract":null,"journal":"PLoS ONE","year":2012,"id":650255,"datarank":0.7454719949364003,"base_score":4.969813299576001,"endowment":4.969813299576001,"self_citation_contribution":0.7454719949364003,"citation_network_contribution":0.0,"self_endowment_contribution":0.7454719949364003,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":143,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1695432,"name":"Dominique Bihan","orcid":null,"position":1,"is_corresponding":false},{"id":1695433,"name":"Francis Chang","orcid":null,"position":2,"is_corresponding":false},{"id":987619,"name":"Paul H. Huang","orcid":"0000-0003-3972-5087","position":3,"is_corresponding":false},{"id":990176,"name":"Richard W. Farndale","orcid":"0000-0001-6130-8808","position":4,"is_corresponding":false},{"id":879556,"name":"Birgit Leitinger","orcid":"0000-0003-2426-1179","position":5,"is_corresponding":false},{"id":534798,"name":"Huifang Xu","orcid":"0000-0002-7077-2896","position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"Discoidin Domain Receptors Promote α1β1- and α2β1-Integrin Mediated Cell Adhesion to Collagen by Enhancing Integrin Activation","abstract":"The discoidin domain receptors, DDR1 and DDR2, are receptor tyrosine kinases that bind to and are activated by collagens. Similar to collagen-binding β1 integrins, the DDRs bind to specific motifs within the collagen triple helix. However, these two types of collagen receptors recognize distinct collagen sequences. While GVMGFO (O is hydroxyproline) functions as a major DDR binding motif in fibrillar collagens, integrins bind to sequences containing Gxx'GEx\". The DDRs are thought to regulate cell adhesion, but their roles have hitherto only been studied indirectly. In this study we used synthetic triple-helical collagen-derived peptides that incorporate either the DDR-selective GVMGFO motif or integrin-selective motifs, such as GxOGER and GLOGEN, in order to selectively target either type of receptor and resolve their contributions to cell adhesion. Our data using HEK293 cells show that while cell adhesion to collagen I was completely inhibited by anti-integrin blocking antibodies, the DDRs could mediate cell attachment to the GVMGFO motif in an integrin-independent manner. Cell binding to GVMGFO was independent of DDR receptor signalling and occurred with limited cell spreading, indicating that the DDRs do not mediate firm adhesion. However, blocking the interaction of DDR-expressing cells with collagen I via the GVMGFO site diminished cell adhesion, suggesting that the DDRs positively modulate integrin-mediated cell adhesion. Indeed, overexpression of the DDRs or activation of the DDRs by the GVMGFO ligand promoted α1β1 and α2β1 integrin-mediated cell adhesion to medium- and low-affinity integrin ligands without regulating the cell surface expression levels of α1β1 or α2β1. Our data thus demonstrate an adhesion-promoting role of the DDRs, whereby overexpression and/or activation of the DDRs leads to enhanced integrin-mediated cell adhesion as a result of higher integrin activation state.","is_dataset_classified":null,"base_score":4.969813299576001,"endowment":4.969813299576001,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"23284937","pmcid":"PMC3527415","openalex_id":"https://openalex.org/W2019624372","authors":[],"funders":[{"funder_name":"Medical Research Council","grant_id":"G0500707","title":"The collagen binding integrins: structure and regulation"},{"funder_name":"Medical Research Council","grant_id":"G0701121","title":"The discoidin domain receptors: collagen binding specificity and cooperation with integrins in cell adhesion / migration"},{"funder_name":"Biotechnology and Biological Sciences Research Council","grant_id":"BB/I014276/1","title":"Quantitative Analysis of Discoidin Domain Receptor 2 Signalling Networks"},{"funder_name":"Wellcome Trust","grant_id":"089028","title":null},{"funder_name":"Biotechnology and Biological Sciences Research Council","grant_id":"BB/I011226/1","title":"Discoidin domain receptor signalling: from crystal structures to mechanisms"},{"funder_name":"Wellcome Trust","grant_id":"unidentified","title":"unidentified"}],"total_grants":6,"fwci":6.1114,"citation_percentile":0.97406639,"influential_citations":0,"citation_trend":[{"year":2013,"count":7},{"year":2014,"count":19},{"year":2015,"count":13},{"year":2016,"count":18},{"year":2017,"count":10},{"year":2018,"count":9},{"year":2019,"count":10},{"year":2020,"count":5},{"year":2021,"count":5},{"year":2022,"count":15},{"year":2023,"count":12},{"year":2024,"count":10},{"year":2025,"count":6},{"year":2026,"count":4}],"oa_status":"gold","license":"cc-by","oa_locations":[{"url":"https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0052209&type=printable","host_type":"journal"},{"url":"https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0052209&type=printable","host_type":"publisher"},{"url":"http://dx.plos.org/10.1371/journal.pone.0052209","host_type":"publisher"},{"url":"https://doi.org/10.1371/journal.pone.0052209","host_type":"journal"},{"url":"https://pubmed.ncbi.nlm.nih.gov/23284937","host_type":"repository"},{"url":"https://doaj.org/article/929bc50cb8f14b9989eee9e09454b993","host_type":"repository"},{"url":"http://europepmc.org/articles/PMC3527415","host_type":"repository"},{"url":"https://figshare.com/articles/dataset/Discoidin_Domain_Receptors_Promote_1_1_and_2_1_Integrin_Mediated_Cell_Adhesion_to_Collagen_by_Enhancing_Integrin_Activation__/115579","host_type":"repository"},{"url":"https://www.ncbi.nlm.nih.gov/pmc/articles/3527415","host_type":"repository"},{"url":"https://europepmc.org/articles/PMC3527415","host_type":"Europe_PMC"},{"url":"https://europepmc.org/articles/PMC3527415?pdf=render","host_type":"Europe_PMC"},{"url":"http://dx.doi.org/10.1371/journal.pone.0052209","host_type":""},{"url":"https://dx.doi.org/10.1371/journal.pone.0052209","host_type":""}],"fields_of_study":["Cell Adhesion Molecules Research","Protease and Inhibitor Mechanisms","Proteoglycans and glycosaminoglycans research","0301 basic medicine","0303 health sciences","03 medical and health sciences"],"mesh_terms":["Discoidin Domain Receptors","Antibodies","Cell Adhesion","Cell Line","Collagen","Humans","Protein Binding","Receptors, Mitogen","Integrins","Receptor Protein-Tyrosine Kinases","Integrin alpha2beta1","Integrin alpha1beta1"],"keywords":["Discoidin domain","DDR1","Collagen receptor","Integrin","Cell biology","Cell adhesion","RGD motif","Cell adhesion molecule","Biology","Chemistry","Receptor","Receptor tyrosine kinase","Signal transduction","Biochemistry","Cell","Integrins","Science","Q","R","Receptor Protein-Tyrosine Kinases","Antibodies","Cell Line","Integrin alpha1beta1","Receptors, Mitogen","Medicine","Humans","Collagen","Integrin alpha2beta1","Discoidin Domain Receptors","Research Article","Protein Binding"],"sdg_mappings":[],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-08-10T05:08:30.460216Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}