<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rogers AW</submitter><funding>NIDCR NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>1383-1390</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6199677</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>97(12)</volume><pubmed_abstract>Temporomandibular joint (TMJ) osteoarthritis (TMJOA) disrupts extracellular matrix (ECM) homeostasis, leading to cartilage degradation. Upregulated a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-5 leads to cleavage of its substrate aggrecan (Acan) and is considered a hallmark of TMJOA. However, most research on ADAMTS5-Acan turnover has focused on hyaline cartilage, not fibrocartilage, which comprises the TMJ. The mandibular condylar cartilage (MCC) of the TMJ is organized in zones, and chondrocytes are arranged in axial rows, yet the molecular mechanisms required to generate the MCC zonal architecture have not been elucidated. Here, we test the hypothesis that ADAMTS5 is required for development of the TMJ MCC. Adamts5&lt;sup>+/+&lt;/sup> and Adamts5&lt;sup>-/-&lt;/sup> murin</pubmed_abstract><journal>Journal of dental research</journal><pubmed_title>The Zonal Architecture of the Mandibular Condyle Requires ADAMTS5.</pubmed_title><pmcid>PMC6199677</pmcid><funding_grant_id>P30-NIGMS-103331</funding_grant_id><funding_grant_id>RO1-HL-121382</funding_grant_id><funding_grant_id>P30-GM-103342</funding_grant_id><funding_grant_id>P30 GM103331</funding_grant_id><funding_grant_id>R01 HL121382</funding_grant_id><funding_grant_id>T32 DE017551</funding_grant_id><funding_grant_id>T32-DE-017551</funding_grant_id><pubmed_authors>Cisewski SE</pubmed_authors><pubmed_authors>Kern CB</pubmed_authors><pubmed_authors>Rogers AW</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Zonal Architecture of the Mandibular Condyle Requires ADAMTS5.</name><description>Temporomandibular joint (TMJ) osteoarthritis (TMJOA) disrupts extracellular matrix (ECM) homeostasis, leading to cartilage degradation. Upregulated a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-5 leads to cleavage of its substrate aggrecan (Acan) and is considered a hallmark of TMJOA. However, most research on ADAMTS5-Acan turnover has focused on hyaline cartilage, not fibrocartilage, which comprises the TMJ. The mandibular condylar cartilage (MCC) of the TMJ is organized in zones, and chondrocytes are arranged in axial rows, yet the molecular mechanisms required to generate the MCC zonal architecture have not been elucidated. Here, we test the hypothesis that ADAMTS5 is required for development of the TMJ MCC. Adamts5&lt;sup>+/+&lt;/sup> and Adamts5&lt;sup>-/-&lt;/sup> murin</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2025-04-04T13:30:19.516Z</modification><creation>2019-11-07T08:01:40Z</creation></dates><accession>S-EPMC6199677</accession><cross_references><pubmed>29879379</pubmed><doi>10.1177/0022034518777751</doi></cross_references></HashMap>