{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["28(5)"],"submitter":["Tang W"],"funding":["Innovative Research Group Project of the National Natural Science Foundation of China"],"pubmed_abstract":["Evidence indicates that mechanical loading plays an important role in osteoarthritis (OA) progression, while the specific pathological changes of the synovium under excessive mechanical loading are unclear. Results showed that excessive mechanical loading caused pro-inflammation of synovial macrophages, which has been confirmed to exist in OA. High Rapgef3 expression level was found in RNA sequencing of RAW246.7 subjected to 0.5 Hz and 20% cyclic tensile strain. We verified this in the synovium of patients with OA and destabilization of the medial meniscus (DMM)-OA mice. Interestingly, the Rapgef3 content of chondrocytes was very low. Primary chondrocytes treated with Rapgef3 alone did not show metabolic phenotype, but an OA phenotype appeared when treated with Rapgef3-stimulated macrophag"],"journal":["iScience"],"pagination":["112131"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12018577"],"repository":["biostudies-literature"],"pubmed_title":["Rapgef3 modulates macrophage reprogramming and exacerbates synovitis and osteoarthritis under excessive mechanical loading."],"pmcid":["PMC12018577"],"pubmed_authors":["Cai DZ","Zhang HY","Yin JB","Huang JL","Liu LL","Li GM","Liu YL","Wu CY","Yang LF","Zhu JJ","Tang W","Lin RG"],"additional_accession":[]},"is_claimable":false,"name":"Rapgef3 modulates macrophage reprogramming and exacerbates synovitis and osteoarthritis under excessive mechanical loading.","description":"Evidence indicates that mechanical loading plays an important role in osteoarthritis (OA) progression, while the specific pathological changes of the synovium under excessive mechanical loading are unclear. Results showed that excessive mechanical loading caused pro-inflammation of synovial macrophages, which has been confirmed to exist in OA. High Rapgef3 expression level was found in RNA sequencing of RAW246.7 subjected to 0.5 Hz and 20% cyclic tensile strain. We verified this in the synovium of patients with OA and destabilization of the medial meniscus (DMM)-OA mice. Interestingly, the Rapgef3 content of chondrocytes was very low. Primary chondrocytes treated with Rapgef3 alone did not show metabolic phenotype, but an OA phenotype appeared when treated with Rapgef3-stimulated macrophag","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 May","modification":"2026-06-01T23:00:25.936Z","creation":"2025-07-01T03:05:15.345Z"},"accession":"S-EPMC12018577","cross_references":{"pubmed":["40276767"],"doi":["10.1016/j.isci.2025.112131"]}}