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dc.contributor.authorLei, Pengfei
dc.contributor.authorDai, Zixun
dc.contributor.authorZhang, Yu S
dc.contributor.authorNiu, Wanting
dc.contributor.authorLi, Kun
dc.contributor.authorWang, Long
dc.contributor.authorHu, Yihe
dc.contributor.authorXie, Jie
dc.contributor.authorZhang, Yu Shrike
dc.contributor.authorLiu, Huan
dc.date.accessioned2019-03-29T20:54:19Z
dc.date.available2019-03-29T20:54:19Z
dc.date.issued2019-03
dc.date.submitted2018-08
dc.identifier.issn1749-799X
dc.identifier.urihttp://hdl.handle.net/1721.1/121127
dc.description.abstractBackground In the ultrahigh molecular weight polyethylene (UHMWPE) prosthetic environment, fibroblasts affected by wear particles have the capacity of osteogenesis to reduce osteolysis. We aimed to assess the effects of macrophages on the osteogenic capability of fibroblasts treated with UHMWPE wear particles. Methods The effect of different concentrations of UHMWPE (0, 0.01, 0.1, and 1 mg/ml, respectively) on macrophage proliferation were validated by MTT assay to determine the optimum one. The fibroblasts viability was further determined in the co-culture system of UHMWPE particles and macrophage supernatants. The experiment was designed as seven groups: (A) fibroblasts only; (B) fibroblasts + 1 mg/ml UHMWPE particles; and (C1–C5) fibroblasts + 1/16, 1/8, 1/4, 1/2, and 1/1 supernatants of macrophage cultures stimulated by 1 mg/ml UHMWPE particles vs. fibroblast complete media, respectively. Alizarin red staining was used to detect calcium accumulation. The expression levels of osteogenic proteins were detected by Western blot and ELISA, including alkaline phosphatase (ALP) and osteocalcin (OCN). Results The concentration of 0.1 mg/ml was considered as the optimum concentration for macrophage proliferation due to the survival rate and was highest among the four concentrations. Fibroblast viability was better in the group of fibroblasts + 1/16 ratio of macrophage supernatants stimulated by 1 mg/ml of UHMWPE particles than the other groups (1:8, 1:4, 1:2, 1:1). ALP and OCN expressions were significantly decreased in the group of fibroblasts + 1/4, 1/2, and 1/1 supernatants stimulated by 1 mg/ml of UHMWPE particles compared with other groups (1/8, 1/16) and the group of fibroblasts + 1 mg/ml UHMWPE (p < 0.5). Conclusions Macrophages are potentially involved in the periprosthetic osteolysis by reducing the osteogenic capability of fibroblasts treated with wear particles generated from UHMWPE materials in total hip arthroplasty.en_US
dc.description.sponsorshipChina Sholarship Council (Grant 201506370173)en_US
dc.description.sponsorshipChina. National Natural Science Foundation (Grant 31200739)en_US
dc.description.sponsorshipChina. National Natural Science Foundation (Grant 31470948)en_US
dc.publisherBioMed Central Ltd.en_US
dc.relation.isversionofhttps://doi.org/10.1186/s13018-019-1119-8en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceBioMed Centralen_US
dc.titleMacrophage inhibits the osteogenesis of fibroblasts in ultrahigh molecular weight polyethylene (UHMWPE) wear particle-induced osteolysisen_US
dc.typeArticleen_US
dc.identifier.citationLei, Pengfei et al. "Macrophage inhibits the osteogenesis of fibroblasts in ultrahigh molecular weight polyethylene (UHMWPE) wear particle-induced osteolysis." Journal of Orthopaedic Surgery and Research 14, 80 (March 2019) https://doi.org/10.1186/s13018-019-1119-8 © The Author(s)en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorLiu, Huan
dc.relation.journalJournal of Orthopaedic Surgery and Researchen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-03-24T04:19:06Z
dc.language.rfc3066en
dc.rights.holderThe Author(s).
dspace.orderedauthorsLei, Pengfei; Dai, Zixun; Zhang, Yu Shrike; Liu, Hua; Niu, Wanting; Li, Kun; Wang, Long; Hu, Yihe; Xie, Jieen_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_CCen_US


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