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Nell-1通过MAPK-ERK信号通路增强钛表面前成骨细胞的成骨分化。

Nell-1 Enhances Osteogenic Differentiation of Pre-Osteoblasts on Titanium Surfaces via the MAPK-ERK Signaling Pathway.

作者信息

Shen Mei-Jie, Wang Ge-Ge, Wang Yu-Zhen, Xie Jing, Ding Xi

机构信息

Department of Stomatology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Department of Stomatology, the First People's Hospital of Tongxiang, Jiaxing, China.

出版信息

Cell Physiol Biochem. 2018;50(4):1522-1534. doi: 10.1159/000494651. Epub 2018 Oct 25.

Abstract

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.

摘要

背景/目的:本研究旨在探讨Nell-1对钛(Ti)表面前成骨细胞成骨行为的影响,并确定其潜在的信号通路。

方法

将不同浓度的Nell-1添加到培养基中,以刺激Ti表面的MC3T3-E1亚克隆14细胞。采用CCK-8比色法检测细胞增殖。分别采用碱性磷酸酶活性(ALP)测定法和酶联免疫吸附测定法(ELISA)评估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。采用蛋白质免疫印迹(WB)测定法分析成骨蛋白和丝裂原活化蛋白激酶(MAPK)信号通路的表达变化。

结果

Nell-1显著提高了Ti表面前成骨细胞中ALP、OCN、Runx2、骨保护素(OPG)、I型胶原(Col-I)和osterix(Osx)的成骨基因和蛋白表达水平。Nell-最佳浓度为100 ng/ml。此外,Nell-1激活了Ti表面MC3T3-E1细胞中的ERK和JNK,但未激活P38。除ALP和Col-I外,ERK抑制剂U0126抑制了Nell-1对成骨标志物表达的促进作用。

结论

一定浓度的Nell-1可通过激活MAPK/ERK信号通路促进Ti表面前成骨细胞的成骨分化。

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