Osteopontin Promotes Expression of Matrix Metalloproteinase 13 through NF-κB Signaling in Osteoarthritis
Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that...
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Published in | BioMed research international Vol. 2016; no. 2016; pp. 1 - 8 |
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Hindawi Publishing Corporation
01.01.2016
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Abstract | Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that OPN promoted the production of MMP13 and activation of NF- κ B pathway by increasing the abundance of p65 and phosphorylated p65 and translocation of p65 protein from cytoplasm to nucleus. Notably, inhibition of NF- κ B pathway by inhibitor suppressed the production of MMP13 induced by OPN treatment. In conclusion, OPN induces production of MMP13 through activation of NF- κ B pathway. |
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AbstractList | Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that OPN promoted the production of MMP13 and activation of NF- κ B pathway by increasing the abundance of p65 and phosphorylated p65 and translocation of p65 protein from cytoplasm to nucleus. Notably, inhibition of NF- κ B pathway by inhibitor suppressed the production of MMP13 induced by OPN treatment. In conclusion, OPN induces production of MMP13 through activation of NF- κ B pathway. Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that OPN promoted the production of MMP13 and activation of NF-κB pathway by increasing the abundance of p65 and phosphorylated p65 and translocation of p65 protein from cytoplasm to nucleus. Notably, inhibition of NF-κB pathway by inhibitor suppressed the production of MMP13 induced by OPN treatment. In conclusion, OPN induces production of MMP13 through activation of NF-κB pathway. Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that OPN promoted the production of MMP13 and activation of NF- Kappa B pathway by increasing the abundance of p65 and phosphorylated p65 and translocation of p65 protein from cytoplasm to nucleus. Notably, inhibition of NF- Kappa B pathway by inhibitor suppressed the production of MMP13 induced by OPN treatment. In conclusion, OPN induces production of MMP13 through activation of NF- Kappa B pathway. Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that OPN promoted the production of MMP13 and activation of NF- κ B pathway by increasing the abundance of p65 and phosphorylated p65 and translocation of p65 protein from cytoplasm to nucleus. Notably, inhibition of NF- κ B pathway by inhibitor suppressed the production of MMP13 induced by OPN treatment. In conclusion, OPN induces production of MMP13 through activation of NF- κ B pathway. Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown. In this study, we found that OA patients had higher abundance of OPN and matrix metalloproteinase 13 (MMP13). In chondrocytes, we showed that OPN promoted the production of MMP13 and activation of NF- B pathway by increasing the abundance of p65 and phosphorylated p65 and translocation of p65 protein from cytoplasm to nucleus. Notably, inhibition of NF- B pathway by inhibitor suppressed the production of MMP13 induced by OPN treatment. In conclusion, OPN induces production of MMP13 through activation of NF- B pathway. |
Author | Xiao, Wenfeng Tu, Min Li, Liangjun Gao, Shuguang Jiang, Wei Zeng, Chao Li, Yusheng Luo, Wei Deng, Zhenhan Lei, Guanghua Wang, Hua |
AuthorAffiliation | 2 Department of Bone and Joint, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen 518020, China 1 Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha 410078, China 3 Department of Orthopaedics, Second People's Hospital of Jingmen, Jingmen 448000, China 4 Department of Joint Surgery, Changsha Central Hospital, Changsha 410000, China |
AuthorAffiliation_xml | – name: 4 Department of Joint Surgery, Changsha Central Hospital, Changsha 410000, China – name: 3 Department of Orthopaedics, Second People's Hospital of Jingmen, Jingmen 448000, China – name: 2 Department of Bone and Joint, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen 518020, China – name: 1 Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha 410078, China |
Author_xml | – sequence: 1 fullname: Luo, Wei – sequence: 2 fullname: Lei, Guanghua – sequence: 3 fullname: Gao, Shuguang – sequence: 4 fullname: Li, Liangjun – sequence: 5 fullname: Tu, Min – sequence: 6 fullname: Zeng, Chao – sequence: 7 fullname: Deng, Zhenhan – sequence: 8 fullname: Wang, Hua – sequence: 9 fullname: Jiang, Wei – sequence: 10 fullname: Li, Yusheng – sequence: 11 fullname: Xiao, Wenfeng |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27656654$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_12677_ACM_2022_127953 crossref_primary_10_1007_s10735_022_10067_9 crossref_primary_10_1139_bcb_2021_0004 crossref_primary_10_3389_fcimb_2022_705647 crossref_primary_10_18632_aging_203707 crossref_primary_10_1155_2020_3428587 |
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Snippet | Osteopontin (OPN) is associated with the severity and progression of osteoarthritis (OA); however, the mechanism of OPN in the pathogenesis of OA is unknown.... |
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Title | Osteopontin Promotes Expression of Matrix Metalloproteinase 13 through NF-κB Signaling in Osteoarthritis |
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