Enhanced in vivo osteogenesis by nanocarrier-fused bone morphogenetic protein-4

被引:28
|
作者
Shiozaki, Yasuyuki [1 ,2 ]
Kitajima, Takashi [4 ]
Mazaki, Tetsuro [1 ,2 ]
Yoshida, Aki [1 ]
Tanaka, Masato [1 ]
Umezawa, Akihiro [5 ]
Nakamura, Mariko [6 ]
Yoshida, Yasuhiro [3 ]
Ito, Yoshihiro [4 ]
Ozaki, Toshifumi [1 ]
Matsukawa, Akihiro [2 ]
机构
[1] Okayama Univ, Dept Orthoped Surg, Okayama 7008558, Japan
[2] Okayama Univ, Dept Pathol & Expt Med, Okayama 7008558, Japan
[3] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Biomat, Okayama 7008558, Japan
[4] RIKEN, Nano Med Engn Lab, Wako, Saitama, Japan
[5] Natl Res Inst Child Hlth & Dev, Okura, Tokyo, Japan
[6] Kibi Int Univ, Jr Coll, Dept Hlth & Welf Program, Takahashi, Okayama, Japan
来源
基金
日本学术振兴会;
关键词
BMP4; bone repair; bone tissue engineering; osteogenesis; OSTEOBLAST DIFFERENTIATION; ALKALINE-PHOSPHATASE; MATRIX; COLLAGEN; FUSION; FIBRONECTIN; SPINE;
D O I
10.2147/IJN.S44124
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose: Bone defects and nonunions are major clinical skeletal problems. Growth factors are commonly used to promote bone regeneration; however, the clinical impact is limited because the factors do not last long at a given site. The introduction of tissue engineering aimed to deter the diffusion of these factors is a promising therapeutic strategy. The purpose of the present study was to evaluate the in vivo osteogenic capability of an engineered bone morphogenetic protein-4 (BMP4) fusion protein. Methods: BMP4 was fused with a nanosized carrier, collagen-binding domain (CBD), derived from fibronectin. The stability of the CBD-BMP4 fusion protein was examined in vitro and in vivo. Osteogenic effects of CBD-BMP4 were evaluated by computer tomography after intramedullary injection without a collagen-sponge scaffold. Recombinant BMP-4, CBD, or vehicle were used as controls. Expressions of bone-related genes and growth factors were compared among the groups. Osteogenesis induced by CBD-BMP4, BMP4, and CBD was also assessed in a bone-defect model. Results: In vitro, CBD-BMP4 was retained in a collagen gel for at least 7 days while BMP4 alone was released within 3 hours. In vivo, CBD-BMP4 remained at the given site for at least 2 weeks, both with or without a collagen-sponge scaffold, while BMP4 disappeared from the site within 3 days after injection. CBD-BMP4 induced better bone formation than BMP4 did alone, CBD alone, and vehicle after the intramedullary injection into the mouse femur. -Bone-related genes and growth factors were expressed at higher levels in CBD-BMP4-treated mice than in all other groups, including BMP4-treated mice. Finally, CBD-BMP4 potentiated more bone formation than did controls, including BMP4 alone, when applied to cranial bone defects without a collagen scaffold. Conclusion: Altogether, nanocarrier-CBD enhanced the retention of BMP4 in the bone, thereby promoting augmented osteogenic responses in the absence of a scaffold. These results suggest that CBD-BMP4 may be clinically useful in facilitating bone formation.
引用
收藏
页码:1349 / 1360
页数:12
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