首页> 外文期刊>Cellular Physiology and Biochemistry >Nell-1 Enhances Osteogenic Differentiation of Pre-Osteoblasts on Titanium Surfaces via the MAPK-ERK Signaling Pathway
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Nell-1 Enhances Osteogenic Differentiation of Pre-Osteoblasts on Titanium Surfaces via the MAPK-ERK Signaling Pathway

机译:Nell-1通过MAPK-ERK信号通路增强钛表面上成骨细胞的成骨分化

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Background/Aims This study aimed to investigate the effect of Nell-1 on the osteogenic behaviors of pre-osteoblasts on titanium (Ti) surfaces and to identify the underlying signaling pathway. Methods Nell-1 at different concentrations was added to culture medium to stimulate MC3T3-E1 subclone 14 on Ti surfaces. A CCK-8 colorimetric assay was used to detect cell proliferation. Alkaline phosphatase activity (ALP) assay and enzyme-linked immunosorbent assay (ELISA) were used to evaluate ALP activity and the osteocalcin (OCN) secretion, respectively. Indicators of osteoblastic differentiation were assessed using real-time polymerase chain reaction analysis (RT-PCR). Western blot (WB) assay was used to analyze the expression changes of the osteogenic proteins and the mitogen-activated protein kinase (MAPK) pathway. Results Nell-1 significantly increased the osteogenic gene and protein expression levels of ALP, OCN, Runx2, osteoprotegerin (OPG), collagen type I (Col-I), and Osterix (Osx) in pre-osteoblasts on Ti surfaces. The optimal concentration of Nell-1 was 100 ng/ ml. In addition, Nell-1 activated ERK and JNK, but not P38, in MC3T3-E1 cells on the Ti surface. Except for ALP and Col-I, the promotive effects of Nell-1 on the expression of osteogenic markers were suppressed by ERK inhibitor U0126. Conclusion Certain concentrations of Nell-1 can promote the osteogenic differentiation of pre-osteoblasts on Ti surfaces by activating the MAPK/ERK signaling pathway.
机译:背景/目的本研究旨在研究Nell-1对成骨细胞在钛(Ti)表面成骨行为的影响,并确定潜在的信号传导途径。方法将不同浓度的Nell-1加入培养基中,刺激Ti表面的MC3T3-E1亚克隆14。使用CCK-8比色测定法检测细胞增殖。碱性磷酸酶活性(ALP)测定和酶联免疫吸附测定(ELISA)分别用于评价ALP活性和骨钙素(OCN)分泌。使用实时聚合酶链反应分析(RT-PCR)评估成骨细胞分化指标。用Western blot(WB)分析成骨蛋白和促分裂原活化蛋白激酶(MAPK)途径的表达变化。结果Nell-1显着增加了成钛细胞表面成骨细胞中ALP,OCN,Runx2,骨保护素(OPG),I型胶原(Col-1)和Osterix(Osx)的成骨基因和蛋白质表达水平。 Nell-1的最佳浓度为100 ng / ml。此外,Nell-1在Ti表面的MC3T3-E1细胞中激活了ERK和JNK,但未激活P38。除ALP和Col-1外,ERK抑制剂U0126抑制Nell-1对成骨标记表达的促进作用。结论一定浓度的Nell-1可以通过激活MAPK / ERK信号通路促进成钛细胞表面成骨细胞的成骨分化。

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