周刊 1997年1月创刊(总第329期) 第12卷 第21期 2008年5月20日出版


牵拉应力在5-氮杂胞苷诱导骨髓间充质干细胞成肌过程中的动态效应*★

何继业,王栋梁,董 海,彭建平,陈晓东


课题背景:①课题得到国家自然科学基金资助,项目名称“骨髓间充质干细胞转化为肌细胞对失神经肌萎缩的影响”,资助总额21万元。②课题取得的成果包括大鼠骨髓间充质干细胞的分离、纯化、培养与鉴定;5-氮杂胞嘧啶核苷与应力刺激诱导骨髓间充质干细胞成肌。已建立相关动物模型,目前正在进行动物体内实验,观察诱导细胞在失神经肌萎缩模型中的作用。

应用要点::①实验首次采用微环境生物力学的方法,单独或与生物化学因素协同对骨髓间质干细胞进行分化诱导,力图调控干预这一分化过程。②FX-4000 Flexercell细胞牵拉系统是国际比较公认应力实验系统。相比自行研制的生物力学设备,其实验结果较有说服力。

偏倚或不足:①实验表明应力能够促进已诱导的骨髓间充质干细胞进一步向肌细胞分化成熟,但究竟采用多大的应力强度及作用时间,且能保持细胞活性还不清楚。②实验之所以采用第4代大鼠骨髓间充质干细胞,是因为据有关文献报道并非任意一代的骨髓间充质干细胞都能够诱导分化为肌细胞,但课题组目前还未就此问题予以实验验证。③体外培养的间充质干细胞衰老较快,如果不能找到很好的培养方法,那么后续体内实验将会收到影响。


摘要
背景:国内外研究发现在一定力学环境下,体外培养的间充质干细胞其增殖分化等一系列生物学特性会发生相应变化。
目的:体外观察5-氮杂胞苷与牵拉应力对大鼠骨髓间充质干细胞向肌细胞分化的调控作用。
设计、时间及地点:2006-01/2007-06在上海交通大学生物力学实验室完成的细胞观察实验。
材料:清洁级3~4周龄雄性SD大鼠30只用于分离培养骨髓间充质干细胞,1~3 d龄SD新生鼠4只用于建立骨骼肌阳性细胞株。化学诱导剂5-氮杂胞苷为Sigma公司产品,牵拉设备FX-4000 Flexercell由美国Flexcell Int公司生产。
方法:将传至第4代的骨髓间充质干细胞接种于Flex 6孔板。①设立5组行成肌家族因子表达Western-Blot检测:第1组细胞单纯经10 μmol/L 5-氮杂胞苷诱导1周;第2~4组细胞以10 μmol/L 5-氮杂胞苷诱导1周后,在1 Hz频率、15%幅度应力条件下分别牵拉12,24,36 h;第5组以新生鼠骨骼肌细胞作为阳性对照。②设立5组行诱导剂及牵拉应力作用的RT-PCR检测:第1组细胞给予1 Hz频率、15%幅度应力牵拉24 h;第2、3组分别经10 μmol/L 5-氮杂胞苷诱导1,2周;第4组细胞经10 μmol/L 5-氮杂胞苷诱导2周后,给与同等应力牵拉24 h;第5组以新生鼠骨骼肌细胞作为阳性对照。
主要观察指标:不同诱导条件及应力牵拉状态下骨髓间充质干细胞成肌家族因子的表达。
结果:①第1组表达成肌因子MyoD与Myf5,成熟肌细胞标志MHC表达不显著;第2~4组MyoD与Myf5的表达明显增强(P < 0.05),且随牵拉时间延长因子的表达逐步增强,MHC表达不显著。②第1组不表达成肌家族因子;第2组表达MyoD、Myf5,第3组表达MyoD、Myf5、desmin,第4组几乎表达所有检测的肌细胞特异性标记。
结论:经5-氮杂胞苷诱导可启动骨髓间充质干细胞向肌细胞分化,单独的牵拉应力不能诱导成肌。牵拉应力可调控5-氮杂胞苷对骨髓间充质干细胞的诱导分化进程,并且与牵拉作用时间成正性相关。
关键词:骨髓间充质干细胞;肌细胞;5-氮杂胞苷;牵拉应力;诱导

何继业,王栋梁,董海,彭建平,陈晓东.牵拉应力在5-氮杂胞苷诱导骨髓间充质干细胞成肌过程中的动态效应[J].中国组织工程研究与临床康复,2008,12(21):4069-4073 [www.zglckf.com/zglckf/ejournal/upfiles/08-21/21k-4069(ps).pdf]


 

 

上海交通大学医学院附属新华医院骨科,上海市 200092

何继业★,男,1976年生,上海市人,汉族,上海交通大学医学院毕业,硕士,主治医师,主要从事肌组织工程方面的研究。
hejiye@gmail.
com

通讯作者:陈晓东,博士,教授,硕士生导师,上海交通大学医学院附属新华医院骨科,上海市 200092 chenxdmd@
yahoo.com

国家自然科学基金(30471748)*

中图分类号:R394.2
文献标识码:A
文章编号:1673-8225
(2008)21-04069-05

收稿日期:2007-10-16 修回日期:2008-02-20 (07-50-10-5585/ZS·Q)


Dynamic effects of stretch stress on bone marrow mesenchymal stem cell differentiation into myoblasts induced by 5-azacytidine

Abstract
BACKGROUND:
In vitro cultured biological characteristics of mesenchymal stem cells (MSCs) changed under a mechanics environment such as proliferation or differentiation.
OBJECTIVE: To observe the regulatory effects of stretch stress on rat bone marrow mesenchymal stem cell (BMSC) differentiation into myoblasts induced by 5-azacytidine.
DESIGN, TIME AND SETTING: The cell experiment was conducted at the Biomechanics Laboratory of Shanghai Jiao Tong University from January 2006 to June 2007.
MATERIALS: Totally 30 male SD rats aged 3-4 weeks of clean grade were selected for BMSC culture. Four neonatal SD rats aged 1-3 days were selected for establishing skeletal muscle positive cell strain. 5-azacytidine was purchased from Sigma, USA and FX-4000 Flexercell was bought from Flexcell Int, USA.
METHODS: Fourth passage of BMSCs was inoculated on the Flex 6-well plate. Western-blot: BMSCs in the group 1 were induced by 10μmol/L 5-azacytidine for 1 week. BMSCs in the groups 2-4 were induced by 10 μmol/L 5-azacytidine for 1 week, and then dragged at a frequency of 1 Hz and an extent of 15% for 12, 24 and 36 hours respectively. Skeletal muscles from neonatal rats in the group 5 were selected as a positive control. Reverse transcriptase-polymerase chain reaction (RT-PCR): BMSCs in the group 1 were dragged at a frequency of 1 Hz and an extent of 15% for 24 hours. BMSCs in the groups 2 and 3 were induced by 10μmol/L 5-azacytidine for 1 and 2 weeks, respectively. BMSCs in the group 4 were induced by 10 μmol/L 5-azacytidine for 2 weeks, and then dragged at a frequency of 1 Hz and an extent of 15% for 24 hours. Skeletal muscles from neonatal rats in the group 5 were selected as a positive control.
MAIN OUTCOME MEASURES: Myogenic family factors of BMSCs under different induction and stress conditions.
RESULTS: MyoD and Myf5 were positive, but MHC was negative in the group 1. MyoD and Myf5 levels were increased in the groups 2-4 (P < 0.05), and increased by prolongation of dragged time. MHC expression was not significant. Myogenic family factors were not detected in the group 1. MyoD and Myf5 were positive in the group 2. MyoD, Myf5 and desmin were positive in the group 3. All myoblast specific markers were found in the group 4.
CONCLUSION: 5-azacytidine can induce the differentiation of BMSCs into myoblasts. Stretch stress alone cannot induce myoblasts. Stretch stress also can adjust the induction of 5-azacytidine on BMSCs, and is positively correlated with stretch time.

He JY, Wang DL, Dong H, Peng JP, Chen XD.Dynamic effects of stretch stress on bone marrow mesenchymal stem cell differentiation into myoblasts induced by 5-azacytidine.Zhongguo Zuzhi Gongcheng Yanjiu yu Linchuang Kangfu 2008;12(21):4069-4073 [www.zglckf.com/zglckf/ejournal/upfiles/08-21/21k-4069(ps).pdf]




Department of Orthopaedics, Xinhua Hospital, Medical College, Shanghai Jiao Tong University, Shanghai 200092, China

He Ji-ye★, Master, Attending physician, Department of Orthopaedics, Xinhua Hospital, Medical College, Shanghai Jiao Tong University, Shanghai 200092, China
hejiye@gmail.com

Correspondence to: Chen Xiao-dong, Doctor, Professor, Tutor of master, Department of Orthopaedics, Xinhua Hospital, Medical College, Shanghai Jiao Tong University, Shanghai 200092, China
chenxdmd@yahoo.
com

Supported by: the National Natural Science Foundation of China, No. 30471748*

Received:2007-10-16
Accepted:2008-02-20

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