组织工程与重建外科杂志 ›› 2010, Vol. 6 ›› Issue (6): 301-305.doi: 10.3969/j.issn.1673-0364.2010.06.001

• 论著 •    下一篇

镁黄长石浸提液影响人脂肪干细胞增殖和成骨分化的实验研究

谷辉杰,巩伦理,张昀,尹烁,常江,崔磊   

  1. 上海交通大学医学院附属第九人民医院整复外科;上海市组织工程国家工程研究中心;上海市中国科学院上海硅酸盐研究所
  • 发布日期:2020-07-23

Experimental Study on the Effect of Extracts of Akermanite on Proliferation and Osteo-Differentiation of Human Adipose-Derived Stem Cells

GU Huijie1,GONG Lunli1,ZHANG Yun1,YIN Shuo2,CHANG Jiang3,CUI Lei1,2   

  1. 1 Department of Plastic and Reconstructive Surgery,Shanghai Ninth People’s Hospital,Shanghai 200011,China;2 National Tissue Engineering Research and Development Center,Shanghai 200241,China;3 Shanghai Institute of Ceramics,Chinese Academy of Science,Shanghai 200050,China
  • Published:2020-07-23
  • Contact: 国家自然科学基金(30672190和30730034)

摘要: 目的通过探讨不同浓度镁黄长石浸提液对人脂肪干细胞(Human adipose-derived stem cells,hADSCs)增殖和成骨分化的影响,初步阐明镁黄长石体外促进hADSCs成骨分化的机制。方法依照ISO/EN 10993-5标准,制备镁黄长石浸提液,将获得的hADSCs培养于不同浓度的浸提液中(1/2、1/4、1/8、1/16、1/32),利用MTT法检测细胞的增殖情况;在成骨诱导条件下,通过碱性磷酸酶染色、活性检测和茜素红染色以及钙离子定量检测,观察不同浓度浸提液对hADSCs成骨特性的影响。结果 1/2、1/4、1/8浓度的浸提液可以浓度依赖性地抑制hADSCs的体外增殖;1/4、1/8、1/16浓度的浸提液可以促进hADSCs的体外成骨分化;碱性磷酸酶染色和活性检测、茜素红染色和钙离子定量检测显示,1/4浓度的浸提液对hADSCs的体外成骨分化促进作用最强,此时的钙、镁和硅离子浓度分别为:2.36 mM、1.11 mM和1.03 mM。结论镁黄长石浸提液中的离子在适当浓度时,可以抑制hADSCs的体外增殖,同时促进hADSCs的体外成骨分化。

关键词: 人脂肪干细胞, 增殖, 成骨分化, 镁黄长石, 浸提液

Abstract: Objective To elucidate the underlying mechanism of the osteo-differentiation of akermanite on human adipose-derived stem cells(hADSCs) via observing the effect of different diluted rate extracts on the proliferation and osteo-differentiation of hDASCs.Methods The original extract was prepared according to the ISO/EN 10993-5 and hDASCs were cultured in the different diluted rate extracts(1/2,1/4,1/8,1/16,1/32).The MTT assay was carried out to quantitatively evaluate the proliferation of the cells.Under the condition of osteo-induction,osteogenic differentiation of hADSCs cultured in the different extracts was detected by ALP expression and calcium deposition.Results The 1/2,1/4,1/8 extracts could concentration-dependently suppress the proliferation of hASCs,while the 1/4,1/8,1/16 extracts could promote the osteogenic differentiation of hADSCs.Among them,the 1/4 extract with the concentration of Ca2+,Mg2+ and Si4+ were 2.36 mM,1.11 mM,1.03 mM,has the optimum one.Conclusion The ions in the extract of akermanite can suppress the proliferation of hADSCs while promoting the osteogenic differentiation of hADSCs in a suitable concentration.

Key words: Human adipose-derived stem cells(hADSCs), Proliferation, Osteogenic differentiation, Akermanite, Extract

中图分类号: