体外负压培养对骨髓间充质干细胞成骨活性的影响
摘要点击次数: 2158   全文下载次数: 1181   投稿时间:2011-05-26    
作者Author单位AddressE-Mail
杨治 YANG Zhi 陕西中医学院西电附属医院骨科,陕西 西安 710077 Department of Orthopaedics, the Xidian Hospital Affiliated to Shaanxi College of Traditional Chinese Medicine, Xi'an 710077, Shaanxi, China xgcgfd@126.com 
朱养均 ZHU Yang-jun 陕西中医学院西电附属医院骨科,陕西 西安 710077 Department of Orthopaedics, the Xidian Hospital Affiliated to Shaanxi College of Traditional Chinese Medicine, Xi'an 710077, Shaanxi, China  
程延 CHENG Yan 陕西中医学院西电附属医院骨科,陕西 西安 710077 Department of Orthopaedics, the Xidian Hospital Affiliated to Shaanxi College of Traditional Chinese Medicine, Xi'an 710077, Shaanxi, China  
尚保生 SHANG Bao-sheng 陕西中医学院西电附属医院骨科,陕西 西安 710077 Department of Orthopaedics, the Xidian Hospital Affiliated to Shaanxi College of Traditional Chinese Medicine, Xi'an 710077, Shaanxi, China  
常瑞 CHANG Rui 陕西中医学院西电附属医院骨科,陕西 西安 710077 Department of Orthopaedics, the Xidian Hospital Affiliated to Shaanxi College of Traditional Chinese Medicine, Xi'an 710077, Shaanxi, China  
何鹏 HE Peng 陕西中医学院西电附属医院骨科,陕西 西安 710077 Department of Orthopaedics, the Xidian Hospital Affiliated to Shaanxi College of Traditional Chinese Medicine, Xi'an 710077, Shaanxi, China  
张银刚 ZHANG Yin-gang 西安交通大学第一附属医院骨科  
期刊信息:《中国骨伤》2011年,第24卷,第12期,第1024-1027页
DOI:10.3969/j.issn.1003-0034.2011.12.014
基金项目:国家自然基金资助项目(编号:30973063);陕西省卫生厅科研基金(编号:2010D23);西安市卫生局科技立项 (编号:J2010B31)
中文摘要:

目的:探讨体外负压培养对骨髓间充质干细胞(bone marrow-derived stroma cells,BMSCs)成骨活性的影响。

方法:取第3代BMSCs分为实验组和对照组,实验组进行间歇性负压培养,设置压力为17 kPa,每次30 min,每日4次,干预2周;对照组于普通CO2培养箱中常规培养。倒置显微镜下观察细胞形态,检测ALP活性,免疫组织化学检测Ⅰ型胶原的表达,RT-PCR检测2周后以及终止负压后1、2、3 d 骨保护素(osteoprotegerin,OPG) mRNA和骨保护素配体(osteoprotegerin ligand,OPGL) mRNA表达水平。

结果:诱导2周后,BMSCs呈现出显著的成骨细胞特性,与对照组比较,ALP活性显著增加,Ⅰ型胶原表达阳性,实验组细胞OPG mRNA表达水平显著提高,OPGL mRNA表达水平显著降低,且差异均有统计学意义(P<0.05).负压终止后3 d,两组细胞OPG mRNA和OPGL mRNA表达水平差异无统计学意义 (P>0.05).

结论:体外负压培养可以提高BMSCs成骨活性。
【关键词】间充质干细胞  骨髓  成骨细胞  细胞培养技术
 
Effects of negative pressure on osteogenesis in human bone marrow-derived stroma cells cultured in vitro
ABSTRACT  

Objective: To investigate effects of intermittent negative pressure on osteogenesis in human bone marrow-derived stroma cells(BMSCs) cultured in vitro.

Methods: The third passage cells were divided into negative pressure treatment group and control group. The cells in the treatment group were induced by negative pressure intermittently(pressure:17 kPa,30 min per time,and four times of each day). The cells in the control group were cultured in conventional condition. The osteogenesis of BMSCs was examined by phase-contrast microscopy. The alkaline phosphatase(ALP) activities were determined. The expression of collagen type I was detected by immunohistochemistry method. The mRNA expressions of osteoprotegerin (OPG) and osteoprotegerin ligand (OPGL) in BMSCs were analyzed by real-time polymerase chain reaction (PCR).

Results: BMSCs showed a typical appearance of osteoblast after 2 weeks of induction by intermittent negative pressure. The activity of ALP increased significantly,and the expression of collagen type I was positive. In the treatment group,the mRNA expression of OPG increased significantly (P<0.05) and the mRNA expression of OPGL decreased significantly (P<0.05) after 2 weeks,compared with the control. However,3 days after the exposure to 2-week negative pressure,these were no significantly different from that of the control group(P>0.05).

Conclusion: Intermittent negative pressure could promote osteogenesis in BMSCs in vitro.
KEY WORDS  Mesenchymal stem cells  Bone marrow  Osteoblasts  Cell culture techniques
 
引用本文,请按以下格式著录参考文献:
中文格式:杨治,朱养均,程延,尚保生,常瑞,何鹏,张银刚.体外负压培养对骨髓间充质干细胞成骨活性的影响[J].中国骨伤,2011,24(12):1024~1027
英文格式:YANG Zhi,ZHU Yang-jun,CHENG Yan,SHANG Bao-sheng,CHANG Rui,HE Peng,ZHANG Yin-gang.Effects of negative pressure on osteogenesis in human bone marrow-derived stroma cells cultured in vitro[J].zhongguo gu shang / China J Orthop Trauma ,2011,24(12):1024~1027
阅读全文  下载  查看/发表评论  下载PDF阅读器
关闭




版权所有:《中国骨伤》杂志社京ICP备12048066号-2  版权声明
地址:北京市东直门内南小街甲16号,100700
电话:010-64089487 传真:010-64089792 Email:zggszz@sina.com

京公网安备 11010102004237号