Three-dimensional polycaprolactone-hydroxyapatite scaffolds combined with bone marrow cells for cartilage tissue engineering

被引:20
作者
Wei, Bo [1 ,2 ,3 ]
Yao, Qingqiang [1 ,2 ,3 ]
Guo, Yang [1 ,2 ,3 ]
Mao, Fengyong [1 ,2 ]
Liu, Shuai [1 ,2 ]
Xu, Yan [1 ,2 ,3 ]
Wang, Liming [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Nanjing Hosp 1, Dept Orthoped Surg, Nanjing 210006, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Cartilage Regenerat Ctr, Nanjing Hosp 1, Nanjing 210006, Jiangsu, Peoples R China
[3] Nanjing Med Univ, China Korea United Cell Therapy Ctr, Nanjing Hosp 1, Nanjing 210006, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Polycaprolactone; hydroxyapatite; bone marrow cells; cartilage tissue engineering; three dimensional; FULL-THICKNESS DEFECTS; ARTICULAR-CARTILAGE; IN-VITRO; CHONDRAL DEFECTS; REPAIR; JOINT; KNEE; TRANSPLANTATION; MICROFRACTURE; DESIGN;
D O I
10.1177/0885328215575762
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The goal of this study was to investigate the chondrogenic potential of three-dimensional polycaprolactone-hydroxyapatite (PCL-HA) scaffolds loaded with bone marrow cells invitro and the effect of PCL-HA scaffolds on osteochondral repair invivo. Here, bone marrow was added to the prepared PCL-HA scaffolds and cultured in chondrogenic medium for 10 weeks. Osteochondral defects were created in the trochlear groove of 29 knees in 17 New Zealand white rabbits, which were then divided into four groups that underwent: implantation of PCL-HA scaffolds (left knee, n=17; Group 1), microfracture (right knee, n=6; Group 2), autologous osteochondral transplantation (right knee, n=6; Group 3), and no treatment (right knee, n=5; Control). Extracellular matrix produced by bone marrow cells covered the surface and filled the pores of PCL-HA scaffolds after 10 weeks in culture. Moreover, many cell-laden cartilage lacunae were observed, and cartilage matrix was concentrated in the PCL-HA scaffolds. After a 12-week repair period, Group 1 showed excellent vertical and lateral integration with host bone, but incomplete cartilage regeneration and matrix accumulation. An uneven surface of regenerated cartilage and reduced distribution of cartilage matrix were observed in Group 2. In addition, abnormal bone growth and unstable integration between repaired and host tissues were detected. For Group 3, the integration between transplanted and host cartilage was interrupted. Our findings indicate that the PCL-HA scaffolds loaded with bone marrow cells improved chondrogenesis invitro and implantation of PCL-HA scaffolds for osteochondral repairenhanced integration with host bone. However, cartilage regeneration remained unsatisfactory. The addition of trophic factors or the use of precultured cell-PCL-HA constructs for accelerated osteochondral repair requires further investigation.
引用
收藏
页码:160 / 170
页数:11
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