Sponsor
  • ·
  • Chinese Association of
    Integrative Medicine;
    China Academy of Chinese
    Medicine Sciences
Editing
  • ·
  • Editorial Board of
    China Journal of
    Orthopaedics and Traumatology
Publishing
  • ·
  • Publishing House,
    China Journal of
    Orthopaedics and Traumatology
Overseas Distributor
  • ·
  • China International Book
    Trading Corporation
    P.O.Box 399,Beijing,China
    Code No.M587
Mail-order
  • ·
  • Publishing House,
    China Journal of
    Orthopaedics and Traumatology
    No.16A, Nanxiaojie, Dongzhimennei,
    Beijing 100700,China
    Tel:0086-10-84020925
    Fax:0086-10-84036581
    Http://www.zggszz.com
    E-mail:zggszz@sina.com
人脱细胞半月板的制备
Hits: 2056   Download times: 1021   Received:November 20, 2013    
作者Author单位UnitE-Mail
周预 ZHOU Yu 首都医科大学附属北京朝阳医院骨科, 北京 100043 Department of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100043, China zhouyu9711@126.com 
刘玉杰 LIU Yu-jie 解放军总医院骨科, 北京 100853  
黄靖香 HUANG Jing-xiang 解放军总医院骨科, 北京 100853  
王瑞 WANG Rui 首都医科大学附属北京朝阳医院骨科, 北京 100043 Department of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100043, China  
臧磊 ZANG Lei 首都医科大学附属北京朝阳医院骨科, 北京 100043 Department of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100043, China  
海涌 HAI Yong 首都医科大学附属北京朝阳医院骨科, 北京 100043 Department of Orthopaedics, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100043, China  
期刊信息:《中国骨伤》2014年27卷,第3期,第237-239页
DOI:10.3969/j.issn.1003-0034.2014.03.016


目的:研究人脱细胞半月板的制备及其形态结构和生物力学性能。

方法:切取人半月板制备人脱细胞半月板,用HE、甲苯胺蓝、天狼星红、番红花O、AB染色和Hoechst-33258染色等方法进行定性检测,扫描电镜进行形态学观察,用生物力学机测定其在不同压缩比率下的瞬时形变恢复率,最大形变恢复率及最大受压强度。

结果:各种染色均显示细胞陷窝内已无细胞结构,Hoechst-33258染色显示无细胞残留,天狼星红染色为阳性,电镜观察示半月板表面及内部不规则存在空虚的陷窝。人脱细胞半月板的孔隙较大,孔隙直径为80~760 μm,孔隙率在67%以上。生物力学测定其压缩30%时,最大瞬时形变恢复率为(89.62±1.04)%,最大形变恢复率为100%,最大强度是(3.04±0.13)N.

结论:人半月板经去污剂等处理后,去除了细胞成分,保留了三维立体结构的细胞外基质,具有一定的生物力学性能;成功制备的人脱细胞半月板可作为半月板组织工程的支架载体。
[关键词]:人类  半月板,胫骨  脱细胞基质
 
Preparation of human meniscus acellular matrix
Abstract:

Objective: To investigate development of a cell extraction process for preparing human meniscus acellular matrix,and morphology and biomechanical properties.

Methods: Human meniscus were subjected to modified eight-step detergent,then,the specimens were assessed by staining with haematoxylin-eosin,toluidine blue,sirius red,saffron O,alcain blue and hoechst-33258,et al. The ultrastructure of the specimens was observed with scanning electron microscope. Transient recovery rate of deformation,maximal recovery rate of deformation and maximal compressive strength were tested to determine the biomechanical properties of the scaffold.

Results: Every stain confirmed that the celluar constituents of the specimens were removed. The specimens stained positively by staining with sirius red. Lacuna were found irregularly not only on the surface of the meniscus,but also in the meniscus with scanning electron microscope. Pores in the specinmens were large,the diameter of pores was 80 to 760 μm,porosity was over 67%. The transient recovery rate of deformation was(89.62±1.04)%,the maximal recovery rate of deformation was 100% and the maximal compressive strength was(3.04±0.13)N,when the specimens were compressed 30%.

Conclusion: The modified eight-step detergent can remove the immunogenic cell components from human meniscus,in addition,3D extracellular matrix can be retained. The scaffold has good biomechanical properties. This scaffold stands a good chance to be an implant for future tissue engineering of the human meniscus.
KEYWORDS:Humans  Menisci,tibia  Decellularization matrix
 
引用本文,请按以下格式著录参考文献:
中文格式:周预,刘玉杰,黄靖香,王瑞,臧磊,海涌.人脱细胞半月板的制备[J].中国骨伤,2014,27(3):237~239
英文格式:ZHOU Yu,LIU Yu-jie,HUANG Jing-xiang,WANG Rui,ZANG Lei,HAI Yong.Preparation of human meniscus acellular matrix[J].zhongguo gu shang / China J Orthop Trauma ,2014,27(3):237~239
View Full Text  View/Add Comment  Download reader
Close




版权所有:Editorial Office of China Journal of Orthopaedics and Traumatology京ICP备12048066号  版权声明
地址:No.16A, Nanxiaojie, Dongzhimennei, Beijing 100700, China
电话:0086-10-84036581 传真:0086-10-84036581 Email:zggszz@sina.com