中国组织工程研究 ›› 2010, Vol. 14 ›› Issue (40): 7580-7582.doi: 10.3969/j.issn.1673-8225.2010.40.039

• 干细胞基础实验 basic experiments of stem cells • 上一篇    下一篇

当归多糖对体外造血微环境中肌卫星细胞增殖的影响 

汪  涛,冯  莉,王晓玲,宋海林   

  1. 天津中医药大学中医学院组织学与胚胎学教研室,天津市  300193 
  • 出版日期:2010-10-01 发布日期:2010-10-01
  • 作者简介:汪涛,女,1962年生,上海市人,汉族,1983年毕业,副教授,硕士生导师,主要从事干细胞生物学的研究。
  • 基金资助:

    天津市高等学校科技发展基金计划项目(20060301);国家自然基金面上项目(30772881)。

Effects of angelica polysaccharides on the proliferation of mouse skeletal muscle satellite cells in hematopoietic microenvironments in vitro

Wang Tao, Feng Li, Wang Xiao-ling, Song Hai-lin   

  1. Department of Histology and Embryology, Tianjin College of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin  300193, China
  • Online:2010-10-01 Published:2010-10-01
  • About author:Wang Tao, Associate professor, Master’s supervisor, Department of Histology and Embryology, Tianjin College of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China wangtao6112@163.com
  • Supported by:

     the Fund for High School Science and Technology Planning Project of Tianjin, No. 20060301*; the National Natural Science Foundation of China (General Program), No. 30772881*

摘要:

背景:肌卫星细胞是造血功能重建最有希望的种子细胞来源。当归多糖对造血干细胞和造血祖细胞的增殖分化存在显著的促进作用,也可以有效改变肌卫星细胞的生长特性。
目的:观察当归多糖对不同培养条件下乳鼠骨骼肌卫星细胞增殖的影响。
方法:分离小鼠肌卫星细胞,培养5 d后采用α-肌动蛋白免疫细胞化学鉴定。将细胞接种于96孔板培养24 h,使细胞同步化;将细胞分为空白对照组,骨髓基质细胞培养上清组,加入含50,100,200,300,400 mg/L当归多糖的DMEM/F12培养基实验组及经50,100,200,300,400 mg/L当归多糖干预后骨髓基质细胞条件培养基组。经实验处理后采用MTT法检测各组细胞的增殖活性。
结果与结论:分离培养的骨骼肌卫星细胞呈α-肌动蛋白染色阳性,通过MTT法检测发现,经不同浓度当归多糖干预后的骨髓基质细胞条件培养基培养的各组肌卫星细胞增殖显著。且经当归多糖干预的骨髓基质细胞条件培养基可以有效改变肌卫星细胞的生长特性,并呈剂量依赖性。

关键词: 肌卫星细胞, 当归多糖, 造血微环境, 增殖

Abstract:

BACKGROUND: It is hopeful that skeletal muscle satellite cells (SMSCs) can be served as seed cells for hematopoietic reconstitution. Angelica polysaccharides (APS) can not only promote hematopoietic stem cells and hematopoietic progenitor cells proliferation and differentiation, but also change the growth characteristics of SMSCs.
OBJECTIVE: To investigate the effects of APS on the proliferation of mouse SMSCs in different culture environments.
METHODS: SMSCs were procured by a modified method from new born mouse. The α-actin protein of the SMSCs was examined by immunohistochemistry at 5 days after culture. SMSCs were cultured and synchronized for 24 hours in the 96-well plate. After that, SMSCs were assigned into the blank control group, marrow stroma cell supernatant group, APS DMEM/F12 groups (contained 50, 100, 200, 300, 400 mg/L APS) and the marrow stroma cell conditioned medium (disposed by 50, 100, 200, 300, 400 mg/L APS in DMEM/F12). The proliferation of SMSCs was determined by MTT.

RESULTS AND CONCLUSION: The α-actin was positive in the cultured SMSCs. MTT results demonstrated that, SMSCs showed a proliferative property in the marrow stroma cell conditioned medium groups. Additionally, the marrow stroma cell conditioned medium can effectively alter growth characteristics of SMSCs in a dose-dependent manner.

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