CAJ | 학술논문

目的探讨氟对大鼠成骨细胞胰岛素样生长因子-1 (IGF-1)和受体mRNA、蛋白表达的影响.方法应用酶消化法分离SD大鼠成骨细胞,取第2代成骨细胞,加入不同浓度[0(对照)、10-7、10-6、10-5、10-4、10-3 mol/L]的氟(F-),在培养24、48 h时采用免疫放射法检测成骨细胞培养液中IGF-1含量；荧光定量PCR法检测成骨细胞IGF-1受体mRNA表达；Western blot法检测成骨细胞IGF-1受体蛋白表达.结果 ①随染氟剂量增加,培养24、48 h的成骨细胞培养液中IGF-1含量有先升后降的趋势,24 h时10-6 mol/L组IGF-1含量[(65.45±4.84)ng/L]最高,与对照组[(38.83±3.48)ng/L]比较,差异有统计学意义(P＜ 0.05);48 h时10-5mol/L组IGF-1含量[(59.14±1.53)ng/L]最高,与对照组[(33.79±1.84)ng/L]比较,差异有统计学意义(P＜0.05).②24、48 h 10-5 mol/L组成骨细胞IGF-1受体mRNA表达(0.0055±0.0004、0.0262±0.0040)明显高于相应对照组(0.0022±0.0001、0.0073±0.0008,P均＜0.05).③随染氟剂量增加,培养24、48 h的成骨细胞IGF-1受体蛋白表达有先升后降的趋势,其中24 h 10-5 mol/L组(1.39±0.16)与对照组(0.86±0.12)比较,差异有统计学意义(P＜0.05),48 h各染氟组与对照组比较,差异无统计学意义(P均＞0.05).结论氟可影响大鼠成骨细胞IGF-1和受体mRNA、蛋白表达,提示IGFs信号传导通路系统对氟调控骨代谢有重要作用.
목적 탐토불대대서성골세포이도소양생장인자-1 (IGF-1)화수체mRNA、단백표체적영향.방법 응용매소화법분리SD대서성골세포,취제2대성골세포,가입불동농도[0(대조)、10-7、10-6、10-5、10-4、10-3 mol/L]적불(F-),재배양24、48 h시채용면역방사법검측성골세포배양액중IGF-1함량；형광정량PCR법검측성골세포IGF-1수체mRNA표체；Western blot법검측성골세포IGF-1수체단백표체.결과 ①수염불제량증가,배양24、48 h적성골세포배양액중IGF-1함량유선승후강적추세,24 h시10-6 mol/L조IGF-1함량[(65.45±4.84)ng/L]최고,여대조조[(38.83±3.48)ng/L]비교,차이유통계학의의(P＜ 0.05);48 h시10-5mol/L조IGF-1함량[(59.14±1.53)ng/L]최고,여대조조[(33.79±1.84)ng/L]비교,차이유통계학의의(P＜0.05).②24、48 h 10-5 mol/L조성골세포IGF-1수체mRNA표체(0.0055±0.0004、0.0262±0.0040)명현고우상응대조조(0.0022±0.0001、0.0073±0.0008,P균＜0.05).③수염불제량증가,배양24、48 h적성골세포IGF-1수체단백표체유선승후강적추세,기중24 h 10-5 mol/L조(1.39±0.16)여대조조(0.86±0.12)비교,차이유통계학의의(P＜0.05),48 h각염불조여대조조비교,차이무통계학의의(P균＞0.05).결론 불가영향대서성골세포IGF-1화수체mRNA、단백표체,제시IGFs신호전도통로계통대불조공골대사유중요작용.
Objective To explore the influence of fluorine on mRNA and protein expression of the insulin-like growth factor-1 (IGF-1) and its receptor of rat osteoblasts.Methods Osteoblasts were isolated from rat bone by enzyme digestion.Different fluorine concentration [0 (control),10-7,10-6,10-5,10-4,10-3 mol/L] was add to the second generation osteoblasts.The IGF-1 in the culture medium was determined by radioimmunoassay (RIA) at different fluorine concentration and different time (24,48 h).The expression of IGF-1 receptor was measured by the method of fluorescent quantitation PCR and the expression of protein IGF-1 receptor was measured by Western blotting.Results ①With increased dose of fluoride exposure,IGF-1 concentration in the osteoblastic culture medium increased first and then decreased at 24,48 h,respectively.Compared to the control group [(38.83 ± 3.48)ng/L],IGF-1 concentration of the 24 h 10-6 mol/L group[(65.45 ± 4.84)ng/L] was higher,and the difference was statistically significant(P ＜ 0.05).The same result was also shown in the 48 h 10-5 mol/L group [(59.14 ± 1.53)ng/L] to its corresponding control group [(33.79 ± 1.84)ng/L,P ＜ 0.05].②The mRNA expression of IGF-1 receptor of the 24,48 h 10-5 mol/L groups (0.0055 ± 0.0004,0.0262 ± 0.0040) was significantly higher than their corresponding control groups (0.0022 ± 0.0001,0.0073 ± 0.0008,all P ＜ 0.05).③With increased dose of fluoride exposure,the protein expression of IGF-1 receptor increased first and then decreased ;the expression of 24 h 10-5 mol/L group (1.39 ± 0.16) was compared with the corresponding control group (0.86 ±0.12),and the difference was statistically significant (P ＜ 0.05) ; the expression of 48 h every fluorine group was also compared with the corresponding control group,and the difference was not statistically significant(all P＞ 0.05).Conclusions Fluorine can affect the mRNA and protein expression of osteoblastic IGF-1 and its receptor.It indicates that IGFS signal transduction pathways play an important role in fluorine regulation of bone metabolism.