Lu Li, Wu Liang, Chen Jun, Lin Xiao-hui, Wan Chao, Li Qing-nan
Guangdong Key Laboratory of Pharmaceutical Bioactive Substances, School of Life Science and Biopharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2011 Nov;31(11):1871-4.
To study the effects of sodium on rat osteoblast function and explore the role of epithelial sodium channel (ENaC) in such effects.
The proliferation and differentiation of rat osteoblasts were evaluated following treatment with 1×10(-4) mol/L to 1 mol/L Na(+). The mRNA expressions of the osteogenic genes and ENaC-α gene in the treated cells were assessed using RT-PCR.
Within the concentration of 1×10(-4) mol/L to 1 mol/L, Na(+) showed a two-way effect on the osteoblasts: low-concentration Na(+) (1×10(-4) mol/L) significantly promoted osteoblast differen- tiation, while at higher concentrations (0.5 and 1 mol/L), Na(+) produced an opposite effect. Sodium did not significantly affect osteoblast proliferation. Low-concentration Na(+) significantly increased the transcription of Cbfa1, OPN and OC, while high concentrations of Na(+) decreased their transcription. Low-concentration Na(+) also enhanced the mRNA expression of ENaC-α, but high-concentration Na(+) treatment lowered ENaC-α mRNA expression.
Na(+) displays a direct dose-related effect on osteoblasts by affecting its differentiation, osteogenic gene expression profile, and ENaC-α gene expression, suggesting the involvement of ENaC in Na(+)-mediated functional modulation of rat osteoblasts.
研究钠对大鼠成骨细胞功能的影响,并探讨上皮钠通道(ENaC)在此类影响中的作用。
用1×10⁻⁴mol/L至1mol/L的Na⁺处理大鼠成骨细胞后,评估其增殖和分化情况。使用逆转录聚合酶链反应(RT-PCR)检测处理后细胞中成骨基因和ENaC-α基因的mRNA表达。
在1×10⁻⁴mol/L至1mol/L的浓度范围内,Na⁺对成骨细胞呈现双向作用:低浓度Na⁺(1×10⁻⁴mol/L)显著促进成骨细胞分化,而在较高浓度(0.5和1mol/L)时,Na⁺产生相反作用。钠对成骨细胞增殖无显著影响。低浓度Na⁺显著增加Cbfa1、OPN和OC的转录,而高浓度Na⁺则降低它们的转录。低浓度Na⁺还增强ENaC-α的mRNA表达,但高浓度Na⁺处理降低ENaC-α mRNA表达。
Na⁺通过影响成骨细胞的分化、成骨基因表达谱和ENaC-α基因表达,对其显示出直接的剂量相关效应,提示ENaC参与Na⁺介导的大鼠成骨细胞功能调节。