脂肪细胞因子促进人体颌骨骨髓干细胞的脂肪生成

Adiponectin Promotes Human Jaw Bone Marrow Stem Cell Osteogenesis
2016-10-13 08:07发表评论
作者:Pu, Y., Wu, H. , Lu, S., Hu, H., Li, D., Wu, Y., Tang, Z.
机构: 北京大学口腔医学院暨口腔医院综合治疗二科
期刊: J DENT RES2016年7月7期95卷

Human jaw bone marrow mesenchymal stem cells (h-JBMMSCs) are multipotent progenitor cells with osteogenic differentiation potential. The relationship between adiponectin (APN) and the metabolism of h-JBMMSCs has not been fully elucidated, and the underlying mechanism remains unclear. The aim of the study was to investigate the effect and mechanism of APN on h-JBMMSC metabolism. h-JBMMSCs were obtained from the primary culture of human jaw bones and treated with or without APN (1 μg/mL). Osteogenesis-related gene expression was evaluated by real-time polymerase chain reaction (PCR), alkaline phosphatase (ALP) activity assay, and enzyme-linked immunosorbent assay (ELISA). To further investigate the signaling pathway, mechanistic studies were performed using Western blotting, immunofluorescence, lentiviral transduction, and SB202190 (a specific p38 inhibitor). Alizarin Red staining showed that APN promoted h-JBMMSC osteogenesis. Real-time PCR, ALP assay, and ELISA showed that ALP, osteocalcin (OCN), osteopontin, and integrin-binding sialoprotein were up-regulated in APN-treated cells compared to untreated controls. Immunofluorescence revealed that adaptor protein containing a pleckstrin homology domain, phosphotyrosine domain, and leucine zipper motif (APPL1) translocated from the nucleus to the cytoplasm with APN treatment. Additionally, the phosphorylation of p38 mitogen-activated protein kinase (MAPK) increased over time with APN treatment. Moreover, knockdown of APPL1 or p38 MAPK inhibition blocked the expression of APN-induced calcification-related genes including ALP, Runt-related transcription factor 2 (RUNX2), and OCN. Furthermore, Alizarin Red staining of calcium nodes was not increased by the knockdown of APPL1 or p38 inhibition. Our data suggest that this regulation is mediated through the APPL1-p38 MAPK signaling pathway. These findings collectively provide evidence that APN induces the osteogenesis of h-JBMMSCs through APPL1-mediated p38 MAPK activation.

© International & American Associations for Dental Research.

通讯机构:2nd Dental Center, Peking University School and Hospital of Stomatology, B5 Anli Garden, #66 Anli Road, Chao Yang District, Beijing, China
学科代码:口腔医学   关键词:脂肪细胞因子 人体颌骨骨髓干细胞 ,中国作者重要发表 爱思唯尔医学网, Elseviermed
来源: Scopus
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