{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Sheffield ID"],"funding":["NEI NIH HHS","Office of Research and Creative Activities, Brigham Young University"],"pagination":["708"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6018413"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["9"],"pubmed_abstract":["Osteoarthritis (OA) is a debilitating inflammation related disease characterized by joint pain and effusion, loss of mobility, and deformity that may result in functional joint failure and significant impact on quality of life. Once thought of as a simple \"wear and tear\" disease, it is now widely recognized that OA has a considerable metabolic component and is related to chronic inflammation. Defects associated with primary cilia have been shown to be cause OA-like changes in Bardet-Biedl mice. We examined the role of dysfunctional primary cilia in OA in mice through the regulation of the previously identified degradative and pro-inflammatory molecular pathways common to OA. We observed an increase in the presence of pro-inflammatory markers TGFβ-1 and HTRA1 as well as cartilage destructiv"],"journal":["Frontiers in physiology"],"pubmed_title":["Osteoarthritis-Like Changes in Bardet-Biedl Syndrome Mutant Ciliopathy Mice (<i>Bbs1</i><sup>M<i>390</i>R/M<i>390</i>R</sup>): Evidence for a Role of Primary Cilia in Cartilage Homeostasis and Regulation of Inflammation."],"pmcid":["PMC6018413"],"funding_grant_id":["R01 EY011298","R01 EY017168"],"pubmed_authors":["Dorius BK","Suli A","Sheffield ID","McGee MA","Coleman JM","Sanchez AE","Williams C","Baek DY","Rose BJ","Goodman MA","Kooyman DL","Daines JM","Eggett DL","Sheffield VC","Glenn SJ"],"additional_accession":[]},"is_claimable":false,"name":"Osteoarthritis-Like Changes in Bardet-Biedl Syndrome Mutant Ciliopathy Mice (<i>Bbs1</i><sup>M<i>390</i>R/M<i>390</i>R</sup>): Evidence for a Role of Primary Cilia in Cartilage Homeostasis and Regulation of Inflammation.","description":"Osteoarthritis (OA) is a debilitating inflammation related disease characterized by joint pain and effusion, loss of mobility, and deformity that may result in functional joint failure and significant impact on quality of life. Once thought of as a simple \"wear and tear\" disease, it is now widely recognized that OA has a considerable metabolic component and is related to chronic inflammation. Defects associated with primary cilia have been shown to be cause OA-like changes in Bardet-Biedl mice. We examined the role of dysfunctional primary cilia in OA in mice through the regulation of the previously identified degradative and pro-inflammatory molecular pathways common to OA. We observed an increase in the presence of pro-inflammatory markers TGFβ-1 and HTRA1 as well as cartilage destructiv","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018","modification":"2025-04-04T20:43:10.786Z","creation":"2019-03-26T23:44:41Z"},"accession":"S-EPMC6018413","cross_references":{"pubmed":["29971011"],"doi":["10.3389/fphys.2018.00708"]}}