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机械应力对下颌骨源性成骨细胞细胞因子产生的影响。

Effects of mechanical stress on cytokine production in mandible-derived osteoblasts.

机构信息

Departments of Microbiology & Immunology, Kyoto Prefectural University of Medicine Graduate School of Medical Science, Japan.

出版信息

Oral Dis. 2011 Oct;17(7):712-9. doi: 10.1111/j.1601-0825.2011.01832.x. Epub 2011 Jul 20.

Abstract

OBJECTIVE

Mechanical stress is known to be an important factor in the regulation of bone remodeling, and mandibular bone is continuously exposed to mechanical stressors such as occlusal force. Therefore, in this study, we investigated the effects of mechanical stress approaching occlusal force, to which mandible-derived osteoblasts (MDOB) are exposed, on cytokine expression and production using an original hydrostatic pressure apparatus.

MATERIALS AND METHODS

The levels of cytokine in MDOB were examined by real-time RT-PCR, ELISA, and western blotting. In addition, mitogen-activated protein kinase inhibitor for ERK1/2, JNK, and p-38 pathways was used to identify the signal transduction pathway.

RESULTS

Hydrostatic pressure increased the expression of IL-6 and TNF-α mRNA in a magnitude- and time-dependent manner and also enhanced IL-6 and TNF-α protein production. Furthermore, hydrostatic pressure changed the RANKL/OPG ratio in favor of RANKL for both mRNA and protein levels. Specific inhibitor of p-38 pathway but not that of the ERK1/2 and JNK pathways suppressed the up-regulation of RANKL production induced by hydrostatic pressure loading.

CONCLUSION

These results suggest that MDOB play a role in cytokine production in response to mechanical stress and that occlusal force may support the maintenance of mandible bone homeostasis by activating bone remodeling through osteoclastogenesis.

摘要

目的

机械应力是调节骨重塑的重要因素,下颌骨不断受到咀嚼力等机械应力的作用。因此,本研究采用原创的静水压力装置,研究了接近咀嚼力的机械应力对下颌骨源性成骨细胞(MDOB)细胞因子表达和产生的影响。

材料与方法

采用实时 RT-PCR、ELISA 和 Western blot 检测 MDOB 中的细胞因子水平。此外,还使用丝裂原活化蛋白激酶(MAPK)ERK1/2、JNK 和 p38 通路抑制剂来鉴定信号转导通路。

结果

静水压力以幅度和时间依赖的方式增加了 IL-6 和 TNF-α mRNA 的表达,并增强了 IL-6 和 TNF-α 蛋白的产生。此外,静水压力改变了 RANKL/OPG 比值,有利于 RANKL 的 mRNA 和蛋白水平。p38 通路的特异性抑制剂而非 ERK1/2 和 JNK 通路的抑制剂可抑制静水压力负荷诱导的 RANKL 产生的上调。

结论

这些结果表明,MDOB 在细胞因子产生中起作用,以响应机械应力,并且咀嚼力可能通过破骨细胞生成来激活骨重塑,从而支持下颌骨骨稳态的维持。

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