Bone Tissue Response to the Bone-like Tissue Coating on Titunitun

被引:1
作者
Wang Xiaoqi
Yang Xu
Zhang Shuang
Jiang Tao
Zhou Yi
Wang Yining [1 ]
机构
[1] Wuhan Univ, State Key Lab Breeding Base Basic Sci Stomatol Hu, Minist Educ, Sch & Hosp Stomatol, Wuhan 430079, Peoples R China
基金
国家教育部博士点专项基金资助; 中国国家自然科学基金;
关键词
bone regeneration; bone marrow stromal cells; mineralized bone nodules; biomaterials; NODULES FORMED INVITRO; MARROW STROMAL CELLS; IN-VITRO; EXTRACELLULAR-MATRIX; OSTEOBLASTIC DIFFERENTIATION; ENDOSSEOUS IMPLANT; FORMATION ADJACENT; GENE-EXPRESSION; SURFACES; TITANIUM;
D O I
10.1007/s11595-015-1126-5
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The objective of this study was to inestigate the effects of mneralized bone nodules, formed in vitro by bone marrow stromal cells (BMSCs), on the new bone formation in bone defect and on implant surface. The mineralized bone nodules were generated by culture of Lewis rats BMSCs on titanium disks in osteogenic induction medium. The gap-healing animal model was used to create the bone detect facing the disk. The titanium disks in the presence of B group or in the absence of NB group bone nodules were randomly placed into one of the rat distal femurs. This self-control design was used to compare the bone formation in defects and on titanium surface, by Micro-CT, fluorescence staining, histological and histomorphometric analysis. 'f he new bone formation parameters in bone defect area of B group were significantly higher than those of NB group at 2 weeks, including bone volume fraction, trabecular thickness and bone area ratio. The bone nodules pre-stained with Alizarin red disappeared mostly at 2 weeks, while the red fluorescence reappeared in the newly formed bone away from the disk surface. For the bone-implant contact, B group showed lower values than NB group at 2 weeks, but no significant difference was found at 4 weeks. Our results indicate that the mineralized bone nodules can be resorbed in vivo and promote the early osteogenesis in the bone defects, and bone nodules may he applicable for new bone generation in hone defect or modification of tissue engineering scaffold.
引用
收藏
页码:203 / 209
页数:7
相关论文
共 30 条
[1]   Early bone formation adjacent to rough and turned endosseous implant surfaces - An experimental study in the dog [J].
Abrahamsson, I ;
Berglundh, T ;
Linder, E ;
Lang, NP ;
Lindhe, J .
CLINICAL ORAL IMPLANTS RESEARCH, 2004, 15 (04) :381-392
[2]   Matricellular proteins: Extracellular modulators of bone development, remodeling, and regeneration [J].
Alford, Andrea I. ;
Hankenson, Kurt D. .
BONE, 2006, 38 (06) :749-757
[3]   MINERALIZED BONE NODULES FORMED INVITRO FROM ENZYMATICALLY RELEASED RAT CALVARIA CELL-POPULATIONS [J].
BELLOWS, CG ;
AUBIN, JE ;
HEERSCHE, JNM ;
ANTOSZ, ME .
CALCIFIED TISSUE INTERNATIONAL, 1986, 38 (03) :143-154
[4]   De novo alveolar bone formation adjacent to endosseous implants -: A model study in the dog [J].
Berglundh, T ;
Abrahamsson, I ;
Lang, NP ;
Lindhe, J .
CLINICAL ORAL IMPLANTS RESEARCH, 2003, 14 (03) :251-262
[5]   ULTRASTRUCTURAL ANALYSIS OF BONE NODULES FORMED INVITRO BY ISOLATED FETAL-RAT CALVARIA CELLS [J].
BHARGAVA, U ;
BARLEV, M ;
BELLOWS, CG ;
AUBIN, JE .
BONE, 1988, 9 (03) :155-163
[6]   In vitro generated extracellular matrix and fluid shear stress synergistically enhance 3D osteoblastic differentiation [J].
Datta, N ;
Pham, QP ;
Sharma, U ;
Sikavitsas, VI ;
Jansen, JA ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (08) :2488-2493
[7]   Effect of bone extracellular matrix synthesized in vitro on the osteoblastic differentiation of marrow stromal cells [J].
Datta, N ;
Holtorf, HL ;
Sikavitsas, VI ;
Jansen, JA ;
Mikos, AG .
BIOMATERIALS, 2005, 26 (09) :971-977
[8]   Organic-inorganic surface modifications for titanium implant surfaces [J].
de Jonge, Lise T. ;
Leeuwenburgh, Sander C. G. ;
Wolke, Joop G. C. ;
Jansen, John A. .
PHARMACEUTICAL RESEARCH, 2008, 25 (10) :2357-2369
[9]   Structure and mechanical quality of the collagen-mineral nano-composite in bone [J].
Fratzl, P ;
Gupta, HS ;
Paschalis, EP ;
Roschger, P .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (14) :2115-2123
[10]   Third-generation biomedical materials [J].
Hench, LL ;
Polak, JM .
SCIENCE, 2002, 295 (5557) :1014-+