<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Naven MA</submitter><funding>Versus Arthritis</funding><funding>Medical Research Council</funding><funding>Biotechnology and Biological Sciences Research Council</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>3963-3976</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9131279</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(8)</volume><pubmed_abstract>The circadian clock in murine articular cartilage is a critical temporal regulatory mechanism for tissue homeostasis and osteoarthritis. However, translation of these findings into humans has been hampered by the difficulty in obtaining circadian time series human cartilage tissues. As such, a suitable model is needed to understand the initiation and regulation of circadian rhythms in human cartilage. &lt;b>Methods:&lt;/b> We used a chondrogenic differentiation protocol on human embryonic stem cells (hESCs) as a proxy for early human chondrocyte development. Chondrogenesis was validated using histology and expression of pluripotency and differentiation markers. The molecular circadian clock was tracked in real time by lentiviral transduction of human clock gene luciferase reporters. Differentiat</pubmed_abstract><journal>Theranostics</journal><pubmed_title>Development of human cartilage circadian rhythm in a stem cell-chondrogenesis model.</pubmed_title><pmcid>PMC9131279</pmcid><funding_grant_id>R20786</funding_grant_id><funding_grant_id>MR/T016744/1</funding_grant_id><funding_grant_id>BB/W013940/1</funding_grant_id><funding_grant_id>MR/P010709/1</funding_grant_id><funding_grant_id>MR/L004992/1</funding_grant_id><funding_grant_id>MR/L011840/1</funding_grant_id><funding_grant_id>MR/S002553/1</funding_grant_id><funding_grant_id>G0801057</funding_grant_id><funding_grant_id>1791756</funding_grant_id><funding_grant_id>20875</funding_grant_id><pubmed_authors>Pathiranage D</pubmed_authors><pubmed_authors>Bates N</pubmed_authors><pubmed_authors>Humphreys PA</pubmed_authors><pubmed_authors>Cain S</pubmed_authors><pubmed_authors>Woods S</pubmed_authors><pubmed_authors>Smith CA</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zeef LAH</pubmed_authors><pubmed_authors>Wen C</pubmed_authors><pubmed_authors>Kimber SJ</pubmed_authors><pubmed_authors>Naven MA</pubmed_authors><pubmed_authors>Au M</pubmed_authors><pubmed_authors>Meng QJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of human cartilage circadian rhythm in a stem cell-chondrogenesis model.</name><description>The circadian clock in murine articular cartilage is a critical temporal regulatory mechanism for tissue homeostasis and osteoarthritis. However, translation of these findings into humans has been hampered by the difficulty in obtaining circadian time series human cartilage tissues. As such, a suitable model is needed to understand the initiation and regulation of circadian rhythms in human cartilage. &lt;b>Methods:&lt;/b> We used a chondrogenic differentiation protocol on human embryonic stem cells (hESCs) as a proxy for early human chondrocyte development. Chondrogenesis was validated using histology and expression of pluripotency and differentiation markers. The molecular circadian clock was tracked in real time by lentiviral transduction of human clock gene luciferase reporters. Differentiat</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-09T16:39:15.649Z</modification><creation>2024-11-15T12:36:00.955Z</creation></dates><accession>S-EPMC9131279</accession><cross_references><pubmed>35664072</pubmed><doi>10.7150/thno.70893</doi></cross_references></HashMap>