体外
单核细胞
碱性磷酸酶
分泌物
MTT法
脂多糖
化学
细胞因子
刺激
细胞生长
体内
炎症
成骨细胞
细胞培养
分子生物学
免疫学
内分泌学
生物
生物化学
酶
遗传学
生物技术
作者
Haiyan Wang,Hui Deng,Chunyan Xu,Jie Ye,Rongdang Hu
出处
期刊:Chinese Journal of Orthodontics
日期:2011-06-20
卷期号:18 (02): 92-96
标识
DOI:10.3760/cma.j.issn.1674-5760.2011.02.007
摘要
Objective To investigate the influence of Pg-LPS stimulated monocyte (RAW264.7) culture supernatant on the proliferation and alkaline phosphatase (ALP) activity of osteoblastic cells (MC3T3-E1) in vitro. Methods The culture supernatant of monocytes stimulated with Pg-LPS was applied to osteoblasts MC3T3-E1 with different diluted concentrations(10%、20%、30%、40% and 50%) simultaneously for 24 h and 48 h in vitro.The cellular proliferation was assessed by MTT assay, Cellular ALP activity was examined using ALP measurement kit, and the results were statistically analyzed using SPSS 12.0 software package. Results LPS stimulated RAW264.7 to release inflammatory cytokines including IL-1β, IL-6 and TNF-α, whose secretion was in a time and dose dependent manner with the concentration of LPS. After the stimulation of different concentrations of inflammatory supernatant, the proliferation and ALP activity of MC3T3-El cells significantly deceased, both in a concentration-dependent manner. Conclusions These results indicated that the inflammatory cytokine secretion of Pg-LPS stimulated RAW264.7 culture supernatant was similar to the change in vivo with inflammation. The inflammatory supernatant could inhibit the proliferation and ALP activity of osteoblastic cells.
Key words:
LPS; Monocyte; Osteoblasts; Proliferation; ALP activity
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