中国骨质疏松杂志
中國骨質疏鬆雜誌
중국골질소송잡지
CHINESE JOURNAL OF OSTEOPOROSIS
2009年
7期
490-495
,共6页
吴小涛%韦继南%李永刚%MAO Zubin%WANG Huan%LU Jun
吳小濤%韋繼南%李永剛%MAO Zubin%WANG Huan%LU Jun
오소도%위계남%리영강%MAO Zubin%WANG Huan%LU Jun
香豆雌酚%成骨细胞%OPG%骨质疏松
香豆雌酚%成骨細胞%OPG%骨質疏鬆
향두자분%성골세포%OPG%골질소송
Coumestrol%Osteoblasts%Osteoprotegerin%Osteoporosis
目的 观察植物雌激素香豆雌酚对成骨细胞增殖分化的作用并探讨其作用机制.方法 从小鼠颅盖骨获得成骨细胞并用0,10-9~10-5 M香豆雌酚孵育48 h,以17β雌二醇为阳性对照,用酶消化法测定碱性磷酸酶及Ⅰ型胶原含量,放免法测定骨钙素含量,RT-PCR法测定OPG及RANKL mRNA表达情况,Western Blot测定OPG蛋白含量.结果 干预48 h,不同浓度香豆雌酚呈剂量依赖性增加碱性磷酸酶及Ⅰ型胶原含量,10-6 M时达到最大效应(P<0.05),但10-5 M效应有所降低,香豆雌酚轻度增加成骨细胞骨钙素含量,各组间无统计学差异.香豆雌酚呈剂量依赖性增加OPG基因及蛋白的表达(P<0.05),轻度降低RANKL基因的表达.结论 香豆雌酚能增加成骨细胞增殖及分化,可能其部分通过OPG/RANKL发挥作用.
目的 觀察植物雌激素香豆雌酚對成骨細胞增殖分化的作用併探討其作用機製.方法 從小鼠顱蓋骨穫得成骨細胞併用0,10-9~10-5 M香豆雌酚孵育48 h,以17β雌二醇為暘性對照,用酶消化法測定堿性燐痠酶及Ⅰ型膠原含量,放免法測定骨鈣素含量,RT-PCR法測定OPG及RANKL mRNA錶達情況,Western Blot測定OPG蛋白含量.結果 榦預48 h,不同濃度香豆雌酚呈劑量依賴性增加堿性燐痠酶及Ⅰ型膠原含量,10-6 M時達到最大效應(P<0.05),但10-5 M效應有所降低,香豆雌酚輕度增加成骨細胞骨鈣素含量,各組間無統計學差異.香豆雌酚呈劑量依賴性增加OPG基因及蛋白的錶達(P<0.05),輕度降低RANKL基因的錶達.結論 香豆雌酚能增加成骨細胞增殖及分化,可能其部分通過OPG/RANKL髮揮作用.
목적 관찰식물자격소향두자분대성골세포증식분화적작용병탐토기작용궤제.방법 종소서로개골획득성골세포병용0,10-9~10-5 M향두자분부육48 h,이17β자이순위양성대조,용매소화법측정감성린산매급Ⅰ형효원함량,방면법측정골개소함량,RT-PCR법측정OPG급RANKL mRNA표체정황,Western Blot측정OPG단백함량.결과 간예48 h,불동농도향두자분정제량의뢰성증가감성린산매급Ⅰ형효원함량,10-6 M시체도최대효응(P<0.05),단10-5 M효응유소강저,향두자분경도증가성골세포골개소함량,각조간무통계학차이.향두자분정제량의뢰성증가OPG기인급단백적표체(P<0.05),경도강저RANKL기인적표체.결론 향두자분능증가성골세포증식급분화,가능기부분통과OPG/RANKL발휘작용.
Objective To observe the effect of phytoestrogen coumestrol on the function of osteoblast including ALP and osteocalcin type I collagen, OPG and RANKL. Methods Osteoblasts obtained from fetal mouse calvaria and were incubated with coumestrol (0, 10-9-10-5 M) or 17β-Estradiol (10-8 M) for 48 hours. Alkaline phosphatase (ALP) activity and type I collagen contents was measured by enzyme digestion. Osteocalcin production was measured by radioimmunity. OPG and RANKL mRNA level were detected by RT-PCR and OPG protein was determined by Western Blot. Results Treated with coumestrol for 48 hours, ALP activity and type I collagen contents was dose-dependently increased by all kinds concentration of coumestrol and reached peak at 10-6 M (P<0.05) and then decreased slightly when cotreated with 10-5 M coumestrol. Coumestrol increased osteocalcin expression slightly, but there were no significant differences among groups. Coumestrol increased OPG mRNA expression and protein production in dose-dependently manner (P<0.05) and slightly decreased RANKL mRNA expression. Conclusions Coumestrol has an enhancing effect on the proliferation and differentiation of osteoblasts, at least in part, by stimulating OPG/RANKL expression in osteoblasts.