中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2015年
37期
5923-5927
,共5页
吴思敏%刘庆梅%马彦云%王久存%赵东宝
吳思敏%劉慶梅%馬彥雲%王久存%趙東寶
오사민%류경매%마언운%왕구존%조동보
组织构建%骨细胞%骨保护素%R-脊椎蛋白1%Wnt%DKK1%hFOB1.19%成骨细胞%破骨细胞%组织工程%国家自然科学基金
組織構建%骨細胞%骨保護素%R-脊椎蛋白1%Wnt%DKK1%hFOB1.19%成骨細胞%破骨細胞%組織工程%國傢自然科學基金
조직구건%골세포%골보호소%R-척추단백1%Wnt%DKK1%hFOB1.19%성골세포%파골세포%조직공정%국가자연과학기금
背景:研究表明Wnt/β-catenin信号通路活性受抑是类风湿关节炎骨侵蚀的始动因素,增强该通路有望治疗类风湿关节炎关节破坏。R-脊椎蛋白1(RSpo1)可能是Wnt激活剂,尚无人成骨细胞相关研究。<br> 目的:验证R-脊椎蛋白1抑制DKK1促进该细胞的分化成熟。<br> 方法:给予S40转染人成骨细胞株hFOB 1.19 Wnt-3a、R-脊椎蛋白1及Wnt信号通路抑制剂DKK1不同刺激,通过检测细胞增殖、碱性磷酸酶活性及骨保护素水平,观察R-脊椎蛋白1在成骨细胞中的作用。<br> 结果与结论:R-脊椎蛋白1对hFOB 1.19细胞增殖无影响,Wnt-3a上调碱性磷酸酶活性,与R-脊椎蛋白1共刺激可增强该作用;R-脊椎蛋白1可减少DKK1对hFOB1.19细胞碱性磷酸酶活力的抑制作用。R-脊椎蛋白1可提高骨保护素质量浓度,但R-脊椎蛋白1对骨保护素的增强作用大于DKK1对其的抑制作用。提示R-脊椎蛋白1通过抑制DKK1,参与Wnt/β-catenin信号通路,促进成骨细胞分化成熟,分泌骨保护素。
揹景:研究錶明Wnt/β-catenin信號通路活性受抑是類風濕關節炎骨侵蝕的始動因素,增彊該通路有望治療類風濕關節炎關節破壞。R-脊椎蛋白1(RSpo1)可能是Wnt激活劑,尚無人成骨細胞相關研究。<br> 目的:驗證R-脊椎蛋白1抑製DKK1促進該細胞的分化成熟。<br> 方法:給予S40轉染人成骨細胞株hFOB 1.19 Wnt-3a、R-脊椎蛋白1及Wnt信號通路抑製劑DKK1不同刺激,通過檢測細胞增殖、堿性燐痠酶活性及骨保護素水平,觀察R-脊椎蛋白1在成骨細胞中的作用。<br> 結果與結論:R-脊椎蛋白1對hFOB 1.19細胞增殖無影響,Wnt-3a上調堿性燐痠酶活性,與R-脊椎蛋白1共刺激可增彊該作用;R-脊椎蛋白1可減少DKK1對hFOB1.19細胞堿性燐痠酶活力的抑製作用。R-脊椎蛋白1可提高骨保護素質量濃度,但R-脊椎蛋白1對骨保護素的增彊作用大于DKK1對其的抑製作用。提示R-脊椎蛋白1通過抑製DKK1,參與Wnt/β-catenin信號通路,促進成骨細胞分化成熟,分泌骨保護素。
배경:연구표명Wnt/β-catenin신호통로활성수억시류풍습관절염골침식적시동인소,증강해통로유망치료류풍습관절염관절파배。R-척추단백1(RSpo1)가능시Wnt격활제,상무인성골세포상관연구。<br> 목적:험증R-척추단백1억제DKK1촉진해세포적분화성숙。<br> 방법:급여S40전염인성골세포주hFOB 1.19 Wnt-3a、R-척추단백1급Wnt신호통로억제제DKK1불동자격,통과검측세포증식、감성린산매활성급골보호소수평,관찰R-척추단백1재성골세포중적작용。<br> 결과여결론:R-척추단백1대hFOB 1.19세포증식무영향,Wnt-3a상조감성린산매활성,여R-척추단백1공자격가증강해작용;R-척추단백1가감소DKK1대hFOB1.19세포감성린산매활력적억제작용。R-척추단백1가제고골보호소질량농도,단R-척추단백1대골보호소적증강작용대우DKK1대기적억제작용。제시R-척추단백1통과억제DKK1,삼여Wnt/β-catenin신호통로,촉진성골세포분화성숙,분비골보호소。
BACKGROUND:Studies have funded that reduced Wnt/β-catenin signaling is involved in the onset and/or progression of bone erosion in rheumatoid arthritis. It can lead to potential new treatment approaches of bone erosion by enhancing Wnt/β-catenin signaling pathway. R-spondin 1 may act as a Wnt agonist, but there is no study in human osteoblasts. OBJECTIVE:To verify the effect of R-spondin 1 on promoting differentiation and maturation of human osteoblasts by inhibiting DKK1. METHODS:S40-transfected human osteoblast lines, hFOB1.19, were treated with R-spondin 1, Wnt-3a and DKK1 to detecting the proliferation, alkaline phoshpatase activity and osteoprotegerin concentration. RESULTS AND CONCLUSION:R-spondin 1 had no effects on hFOB1.19 cel s. Wnt-3a upregulated the activity of alkaline phoshpatase, which could be enhanced by addition of R-spondin 1. R-spondin 1 could reduce the DKK1-mediated inhibition of alkaline phoshpatase activity in hFOB1.19 cel s. R-spondin 1 increased the concentration of osteoprotegerin, and moreover, the promotion of osteoprotegerin by R-spondin 1 alone was stronger than the inhibition by DKK1. These findings suggest that R-spondin 1 can inhibit DKK1 by Wnt/β-catenin signal pathway to promote the differential and maturation of human osteoblasts to excrete osteoprotegerin.