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论文摘要

成骨细胞中Runx2对机械离心力刺激的响应

Bone morphogenetic protein signal transduction pathway regulates Runx2 expression in MC3T3 -E1 osteoblasts in vitro induced by centrifugation

作者:关键 程宗生 王健平 李德超 邓慧鑫

Author:GUAN Jian, CHENG Zong-sheng, WANG Jian-ping, LI De-chao, DENG Hui-xin

收稿日期:2010-02-25          年卷(期)页码:2010,28(01):38-38-40

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:基因表达,信号转导,离心力,成骨细胞,骨形态发生蛋白,

Key words:gene expression,signal transduction,centrifugation,osteoblasts,bone morphogenetic protein,

基金项目:

黑龙江省青年科学技术专项基金资助项目(QC05C47)

中文摘要

目的研究机械离心力刺激对MC3T3-E1细胞中Runx2表达的影响,探讨成骨细胞将力学刺激转化为生化响应过程中骨形态发生蛋白(BMP)信号转导通路的作用。方法将MC3T3-E1细胞分成A、B、C、D组,分别使用含10%胎牛血清、10%胎牛血清、100 ng·mL-1 Noggin和100 ng·mL-1 Noggin的DEME培养基预处理24 h,对B、D组加载271×g离心力5 min,A、C组不进行离心加力,其余条件相同。30 min后4组分别同时收获细胞,提取总RNA,并逆转录为cDNA,通过实时荧光定量PCR检测Runx2基因表达情况。结果B组Runx2 mRNA表达较A组明显增高(P

英文摘要

Objective To observe the expression of Runx2 in osteoblasts in response to centrifugation in vitro and discuss the function of bone morphogenetic protein(BMP) signal transduction pathway in this course. Methods Cells were divided into four groups, group A, B, C and D, pretreated with DMEM containing 10% fetal bovine serum, 10% fetal bovine serum, 100 ng·mL-1 Noggin and 100 ng·mL-1 Noggin for 24 hours separately. 271×g centrifugation was loaded for 5 min to these groups except group A and C, other conditions were the same. The total RNA of each group were extracted, and reversed transcription to cDNA after 30 min. The expression of Runx2 in response to centrifugation in vitro was analyzed by quantitative real time PCR. Results The expression of Runx2 mRNA in group B was significantly higher than that in group A(P

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