中国骨质疏松杂志
中國骨質疏鬆雜誌
중국골질소송잡지
CHINESE JOURNAL OF OSTEOPOROSIS
2013年
12期
1224-1227,1249
,共5页
刘国岩%徐展望%徐琬梨%张建新%刘彬
劉國巖%徐展望%徐琬梨%張建新%劉彬
류국암%서전망%서완리%장건신%류빈
骨碎补%骨髓间充质干细胞%Cbfα-1%成骨能力
骨碎補%骨髓間充質榦細胞%Cbfα-1%成骨能力
골쇄보%골수간충질간세포%Cbfα-1%성골능력
Rhizoma drynariae%Bone marrow mesenchymal stem cells%Cbf alpha 1%Osteogenesis ability
目的:体外实验研究中药骨碎补对大鼠骨髓间充质干细胞增殖分化及对Cbfα-1表达的影响。方法采用中药干预培养细胞的方法,利用骨碎补单味药物与培养基联合培养大鼠骨髓间充质干细胞( BMSCs ),通过Ⅰ型胶原免疫组化染色检测其促BMSCs成骨分化能力,通过RT-PCR方法进行半定量分析Cbfα-1的表达,探讨中药骨碎补促成骨能力的机制。结果骨碎补药物各组Ⅰ型胶原免疫组化染色检测BMSCs成骨分化能力及RT-PCR检测Cbfα-1的表达均明显优于空白组及条件培养组(P<0.01),0.002 g/ml药物组优于0.02 g/ml及0.0002 g/ml药物组(P<0.05)。结论中药骨碎补可促进BMSCs增殖及成骨分化,使Cbfα1的表达加强。
目的:體外實驗研究中藥骨碎補對大鼠骨髓間充質榦細胞增殖分化及對Cbfα-1錶達的影響。方法採用中藥榦預培養細胞的方法,利用骨碎補單味藥物與培養基聯閤培養大鼠骨髓間充質榦細胞( BMSCs ),通過Ⅰ型膠原免疫組化染色檢測其促BMSCs成骨分化能力,通過RT-PCR方法進行半定量分析Cbfα-1的錶達,探討中藥骨碎補促成骨能力的機製。結果骨碎補藥物各組Ⅰ型膠原免疫組化染色檢測BMSCs成骨分化能力及RT-PCR檢測Cbfα-1的錶達均明顯優于空白組及條件培養組(P<0.01),0.002 g/ml藥物組優于0.02 g/ml及0.0002 g/ml藥物組(P<0.05)。結論中藥骨碎補可促進BMSCs增殖及成骨分化,使Cbfα1的錶達加彊。
목적:체외실험연구중약골쇄보대대서골수간충질간세포증식분화급대Cbfα-1표체적영향。방법채용중약간예배양세포적방법,이용골쇄보단미약물여배양기연합배양대서골수간충질간세포( BMSCs ),통과Ⅰ형효원면역조화염색검측기촉BMSCs성골분화능력,통과RT-PCR방법진행반정량분석Cbfα-1적표체,탐토중약골쇄보촉성골능력적궤제。결과골쇄보약물각조Ⅰ형효원면역조화염색검측BMSCs성골분화능력급RT-PCR검측Cbfα-1적표체균명현우우공백조급조건배양조(P<0.01),0.002 g/ml약물조우우0.02 g/ml급0.0002 g/ml약물조(P<0.05)。결론중약골쇄보가촉진BMSCs증식급성골분화,사Cbfα1적표체가강。
Objective To investigate the effect of traditional Chinese medicine ( TCM) , rhizoma drynariae, on the proliferation and differentiation of rat bone marrow mesenchymal stem cells (BMSCs) and the expression of Cbf alpha1 (Cbfα-1) in vitro. Methods The method of culturing cells with the intervention of TCM was used.Rat BMSCs were cultured with the combination of single drug rhizoma drynariae and the medium.Collagen type I immunohistochemical staining was performed to detect its ability to promote the osteogenesis of BMSCs.The expression of Cbfα-1 was semi-quantitatively analyzed using RT-PCR, in order to investigate the mechanism of rhizoma drynariae promoting osteogenesis.Results The ability to promote the osteogenesis of BMSCs detected using collagen type I immunohistochemical staining and the expression of Cbfα-1 detected using RT-PCR in all rhizoma drynariae drug groups were significantly better than that in blank control group and conditioned culture group ( P<0.01 ) . The effect in the group with 0.002 g/ml of the drug was better than that in the groups with 0.02 g/ml and 0.0002 g/ml of the drug (P<0.05).Conclusion Rhizoma drynariae can promote the proliferation and osteogenesis differentiation of BMSCs and enhance the expression of Cbfα-1.