中国骨质疏松杂志
中國骨質疏鬆雜誌
중국골질소송잡지
CHINESE JOURNAL OF OSTEOPOROSIS
2014年
7期
779-783
,共5页
曾高峰%宗少晖%邹斌%李柯柯
曾高峰%宗少暉%鄒斌%李柯柯
증고봉%종소휘%추빈%리가가
黄精多糖%骨髓间充质干细胞%成骨细胞分化%碱性磷酸酶%骨钙素
黃精多糖%骨髓間充質榦細胞%成骨細胞分化%堿性燐痠酶%骨鈣素
황정다당%골수간충질간세포%성골세포분화%감성린산매%골개소
Polygonatum polysaccharides%Bone marrow derived mesenchymal stem cell%Osteogenic differentiation%ALP%BGP
目的:探讨黄精多糖( PSP)对小鼠骨髓间充质干细胞向成骨细胞分化作用中碱性磷酸酶( alkaline phosphatase,ALP)和骨钙素( bone gla protein,BGP)表达的影响。方法取8周龄雄性BALB/C小鼠1只,无菌操作分离小鼠股骨和胫骨,注射器冲出骨髓制成细胞悬液,传代3次后分为7组用于实验。诱导组细胞采用体积分数为0.1双抗、含不同浓度PSP的血清+IMDM培养,非诱导组细胞采用体积分数为0.1双抗血清+IMDM培养。每天在倒置显微镜下观察各组细胞的生长情况及形态变化。在培养第3,5,7,9,11,13天用四唑盐法(MTT)检测细胞的生长情况并绘制细胞生长曲线。在培养第7天、第14天采用ELISΑ酶联免疫吸附法分别测量细胞碱性磷酸酶( ALP)和骨钙素( BGP)的表达量。结果①小鼠骨髓间充质干细胞经PSP诱导后呈三角形、多角形、不规则状,可重叠生长。②各组细胞生长曲线总体趋势基本相同,在第7,9,11,13天,非诱导组细胞不再生长,而各PSP诱导组细胞均继续生长。③各不同浓度PSP诱导组均比非诱导组高表达ALP和BGP( P<0.01)。结论 PSP可显著促小鼠骨髓间充质干细胞向成骨分化过程中ALP和BGP的表达,且随着浓度的增高该促进作用逐渐增强。
目的:探討黃精多糖( PSP)對小鼠骨髓間充質榦細胞嚮成骨細胞分化作用中堿性燐痠酶( alkaline phosphatase,ALP)和骨鈣素( bone gla protein,BGP)錶達的影響。方法取8週齡雄性BALB/C小鼠1隻,無菌操作分離小鼠股骨和脛骨,註射器遲齣骨髓製成細胞懸液,傳代3次後分為7組用于實驗。誘導組細胞採用體積分數為0.1雙抗、含不同濃度PSP的血清+IMDM培養,非誘導組細胞採用體積分數為0.1雙抗血清+IMDM培養。每天在倒置顯微鏡下觀察各組細胞的生長情況及形態變化。在培養第3,5,7,9,11,13天用四唑鹽法(MTT)檢測細胞的生長情況併繪製細胞生長麯線。在培養第7天、第14天採用ELISΑ酶聯免疫吸附法分彆測量細胞堿性燐痠酶( ALP)和骨鈣素( BGP)的錶達量。結果①小鼠骨髓間充質榦細胞經PSP誘導後呈三角形、多角形、不規則狀,可重疊生長。②各組細胞生長麯線總體趨勢基本相同,在第7,9,11,13天,非誘導組細胞不再生長,而各PSP誘導組細胞均繼續生長。③各不同濃度PSP誘導組均比非誘導組高錶達ALP和BGP( P<0.01)。結論 PSP可顯著促小鼠骨髓間充質榦細胞嚮成骨分化過程中ALP和BGP的錶達,且隨著濃度的增高該促進作用逐漸增彊。
목적:탐토황정다당( PSP)대소서골수간충질간세포향성골세포분화작용중감성린산매( alkaline phosphatase,ALP)화골개소( bone gla protein,BGP)표체적영향。방법취8주령웅성BALB/C소서1지,무균조작분리소서고골화경골,주사기충출골수제성세포현액,전대3차후분위7조용우실험。유도조세포채용체적분수위0.1쌍항、함불동농도PSP적혈청+IMDM배양,비유도조세포채용체적분수위0.1쌍항혈청+IMDM배양。매천재도치현미경하관찰각조세포적생장정황급형태변화。재배양제3,5,7,9,11,13천용사서염법(MTT)검측세포적생장정황병회제세포생장곡선。재배양제7천、제14천채용ELISΑ매련면역흡부법분별측량세포감성린산매( ALP)화골개소( BGP)적표체량。결과①소서골수간충질간세포경PSP유도후정삼각형、다각형、불규칙상,가중첩생장。②각조세포생장곡선총체추세기본상동,재제7,9,11,13천,비유도조세포불재생장,이각PSP유도조세포균계속생장。③각불동농도PSP유도조균비비유도조고표체ALP화BGP( P<0.01)。결론 PSP가현저촉소서골수간충질간세포향성골분화과정중ALP화BGP적표체,차수착농도적증고해촉진작용축점증강。
Objective To observe the effect of polygonatum polysaccharides ( PSP) on the expression of alkaline phosphatase ( ALP) and bone gla protein ( BGP) in the differentiation of the osteoblast by mouse bone marrow derived mesenchymal stem cells ( BMSCs) .Methods A BALB/C male 8-week mouse was selected.The marrow from the femur and the tibia was collected through sterile operation.The 3rd passage cells were collected and divided into 7 groups for the experiment.The cells in induced groups were cultured with 10%penicillin and streptomycin serum, additioned with different concentrations of PSP+IMDM, while cells in non-induced group were cultured with 10%penicillin and streptomycin serum +IMDM.The proliferation and morphologic changes of these cells were observed using inverted microscope everyday.At the 3rd, 5th, 7th, 9th, 11th, and the 13th day of culturing, the proliferation and growth of cells were determined using MTT test.The expression of ALP and BGP was detected using ELISA kit at the 7th day and the 14th day.Results After the induction with PSP, BMSCs presented as triangle, astero-form, polygon, or irregular shape.Clumps and multilayer of cells became evident.The growth curves of cells in each group were roughly the same.At the 7th, 9th, 11th, and the 13th day, cells in non-induced group stopped growing, while the cells in induced groups kept growing.The expression of ALP and BGP in induced groups with different concentrations of PSP was higher than that in the non-induced group.Conclusion PSP can enhance the expression of ALP and BGP during the osteogenic differentitation of BMSCs, especially in a high concentration of PSP.