中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
30期
4797-4803
,共7页
生物材料%骨生物材料%胶原膜%骨髓间充质干细胞%复合培养%细胞增殖%成骨分化%骨组织工程%引导骨组织再生技术
生物材料%骨生物材料%膠原膜%骨髓間充質榦細胞%複閤培養%細胞增殖%成骨分化%骨組織工程%引導骨組織再生技術
생물재료%골생물재료%효원막%골수간충질간세포%복합배양%세포증식%성골분화%골조직공정%인도골조직재생기술
stem cells%col agen%celldifferentiation%bone regeneration
背景:相关实验表明Bio-Gide胶原膜与细胞有良好的生物相容性,但有关与其复合培养干细胞成骨分化能力的报道少见。目的:观察Bio-Gide胶原膜对骨髓间充质干细胞增殖及成骨分化的影响。方法:全骨髓贴壁法体外分离培养兔骨髓间充质干细胞,将第3代兔骨髓间充质干细胞分别接种于覆盖Bio-Gide胶原膜的培养板(实验组)与单纯培养板(对照组)培养。于培养1,4,7,14 d利用CCK-8试剂盒检测细胞增殖;成骨分化诱导培养1,4,7,14 d收集细胞培养液上清,检测细胞碱性磷酸酶活性。结果与结论:两组细胞数量均随着培养时间的增加而不断增加,对照组培养7 d细胞数量明显多于实验组(P<0.05),其他时间点组间比较差异无显著性意义。两组细胞碱性磷酸酶活性均随着培养时间的增加而不断增加,实验组成骨诱导14 d细胞碱性磷酸酶活性高于对照组(P <0.05),其他时间点组间比较差异无显著性意义。表明Bio-Gide胶原膜可促进兔骨髓间充质干细胞的增殖及成骨分化。
揹景:相關實驗錶明Bio-Gide膠原膜與細胞有良好的生物相容性,但有關與其複閤培養榦細胞成骨分化能力的報道少見。目的:觀察Bio-Gide膠原膜對骨髓間充質榦細胞增殖及成骨分化的影響。方法:全骨髓貼壁法體外分離培養兔骨髓間充質榦細胞,將第3代兔骨髓間充質榦細胞分彆接種于覆蓋Bio-Gide膠原膜的培養闆(實驗組)與單純培養闆(對照組)培養。于培養1,4,7,14 d利用CCK-8試劑盒檢測細胞增殖;成骨分化誘導培養1,4,7,14 d收集細胞培養液上清,檢測細胞堿性燐痠酶活性。結果與結論:兩組細胞數量均隨著培養時間的增加而不斷增加,對照組培養7 d細胞數量明顯多于實驗組(P<0.05),其他時間點組間比較差異無顯著性意義。兩組細胞堿性燐痠酶活性均隨著培養時間的增加而不斷增加,實驗組成骨誘導14 d細胞堿性燐痠酶活性高于對照組(P <0.05),其他時間點組間比較差異無顯著性意義。錶明Bio-Gide膠原膜可促進兔骨髓間充質榦細胞的增殖及成骨分化。
배경:상관실험표명Bio-Gide효원막여세포유량호적생물상용성,단유관여기복합배양간세포성골분화능력적보도소견。목적:관찰Bio-Gide효원막대골수간충질간세포증식급성골분화적영향。방법:전골수첩벽법체외분리배양토골수간충질간세포,장제3대토골수간충질간세포분별접충우복개Bio-Gide효원막적배양판(실험조)여단순배양판(대조조)배양。우배양1,4,7,14 d이용CCK-8시제합검측세포증식;성골분화유도배양1,4,7,14 d수집세포배양액상청,검측세포감성린산매활성。결과여결론:량조세포수량균수착배양시간적증가이불단증가,대조조배양7 d세포수량명현다우실험조(P<0.05),기타시간점조간비교차이무현저성의의。량조세포감성린산매활성균수착배양시간적증가이불단증가,실험조성골유도14 d세포감성린산매활성고우대조조(P <0.05),기타시간점조간비교차이무현저성의의。표명Bio-Gide효원막가촉진토골수간충질간세포적증식급성골분화。
BACKGROUND:Bio-Gide col agen membranes show a good biocompatibility with stem cells. But the research on the osteogenetic differentiation of bone marrow mesenchymal stem cells cultured on the Bio-Gide col agen membranes is rarely reported. OBJECTIVE:To observe the effect of Bio-Gide col agen membranes on the proliferation and the osteogenetic differentiation of bone marrow mesenchymal stem cells. METHODS:Bone marrow mesenchymal stem cells from rabbits were isolated and cultured by using the whole bone marrow adherence method in vitro. Passage 3 bone marrow mesenchymal stem cells were selected and seeded on the Bio-Gide col agen membrane pretreated petri dish (experimental group) and simple petri dish (control group). The proliferation of bone marrow mesenchymal stem cells was detected by cellCounting Kit-8 at 1, 4, 7, 14 days. The supernatant of the cells cultured in osteogenic differentiation medium were col ected to detect the activity of alkaline phosphatase at 1, 4, 7, 14 days. RESULTS AND CONCLUSION:The number of bone marrow mesenchymal stem cells in the two groups was increased with the increasing time, and the control group had more cells than the experimental group at 7 days (P<0.05). There was no significant difference between the two groups at other time points. The alkaline phosphatase activity was increased with the increasing culture time, and the experimental group had a higher activity than the control group at 14 days (P<0.05). There was no significant difference between the two groups at other time points. Experimental findings indicate that Bio-Gide col agen membranes can promote the proliferation and the osteogenetic differentiation of bone marrow mesenchymal stem cells.