Capillary vessel network integration by inserting a vascular pedicle enhances bone formation in tissue-engineered bone using interconnected porous hydroxyapatite ceramics

被引:60
作者
Akita, S
Tamai, N
Myoui, A
Nishikawa, M
Kaito, T
Takaoka, K
Yoshikawa, H
机构
[1] Osaka Univ, Grad Sch Med, Dept Orthoped, Suita, Osaka 5650871, Japan
[2] Hoshigaoka Koseinenkin Hosp, Dept Orthoped Surg, Osaka, Japan
[3] Osaka City Univ, Sch Med, Dept Orthoped Surg, Osaka 545, Japan
来源
TISSUE ENGINEERING | 2004年 / 10卷 / 5-6期
关键词
D O I
10.1089/1076327041348338
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The aim of the present study was to investigate the possibility of integrating porous hydroxyapatite (HA) ceramics with a capillary vessel network via insertion of a vascular pedicle, and to determine whether this procedure enhances new bone formation in tissue engineering of bone. First, synthetic interconnected porous HA (IP-CHA) was implanted subcutaneously into rat groin with or without insertion of superficial inferior epigastric vessels. At 6 weeks, IP-CHA with vascular insertion contained thick fibrous connective tissue with a number of large blood vessels that seemed to derive from the inserted vascular bundle. Next, IP-CHA loaded with recombinant human bone morphogenetic protein 2 (BMP, 2 or 10 mug/block) was implanted with or without vascular insertion. At 3 weeks, IP-CHA/BMP (10 mug) composite with vascular insertion exhibited abundant new bone formation in the pores of the deep portion close to the inserted vessels. In contrast, IP-CHA/BMP (10 mug) without vascular insertion showed poor bone formation. Histomorphometric analysis demonstrated that vascular insertion significantly increased new bone formation. In IP-CHAs with a lower dose of BMP (2 mug), no bone formation was found, with or without vascular insertion. These results suggest that the present system of integrating a vascular network with IP-CHA is a useful technique for bone tissue engineering.
引用
收藏
页码:789 / 795
页数:7
相关论文
共 24 条
[11]   The effect of blood supply in muscle and an elevated muscle flap on endogenous tissue-engineered bone by rhBMP-2 in the rat [J].
Kusumoto, K ;
Bessho, K ;
Fujimura, K ;
Akioka, J ;
Okubo, Y ;
Ogawa, Y ;
Iizuka, T .
ANNALS OF PLASTIC SURGERY, 2000, 45 (04) :408-414
[12]   Antiangiogenic agent (TNP-470) inhibition of ectopic bone formation induced by bone morphogenetic protein-2 [J].
Mori, S ;
Yoshikawa, H ;
Hashimoto, J ;
Ueda, T ;
Funai, H ;
Kato, M ;
Takaoka, K .
BONE, 1998, 22 (02) :99-105
[13]  
NAKANO K, 1992, SPINE, V17, pS41
[14]  
Nakase T, 2000, HISTOCHEM CELL BIOL, V114, P21
[15]  
Norman Maria E., 1994, Clinical Materials, V17, P85, DOI 10.1016/0267-6605(94)90016-7
[16]  
Noshi T, 2000, J BIOMED MATER RES, V52, P621
[17]   Tissue-engineered bone regeneration [J].
Petite, H ;
Viateau, V ;
Bensaïd, W ;
Meunier, A ;
de Pollak, C ;
Bourguignon, M ;
Oudina, K ;
Sedel, L ;
Guillemin, G .
NATURE BIOTECHNOLOGY, 2000, 18 (09) :959-963
[18]   Repair of large bone defects with the use of autologous bone marrow stromal cells [J].
Quarto, R ;
Mastrogiacomo, M ;
Cancedda, R ;
Kutepov, SM ;
Mukhachev, V ;
Lavroukov, A ;
Kon, E ;
Marcacci, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (05) :385-386
[19]   A biodegradable polymer as a cytokine delivery system for inducing bone formation [J].
Saito, N ;
Okada, T ;
Horiuchi, H ;
Murakami, N ;
Takahashi, J ;
Nawata, M ;
Ota, H ;
Nozaki, K ;
Takaoka, K .
NATURE BIOTECHNOLOGY, 2001, 19 (04) :332-335
[20]   Novel hydroxyapatite ceramics with an interconnective porous structure exhibit superior osteoconduction in vivo [J].
Tamai, N ;
Myoui, A ;
Tomita, T ;
Nakase, T ;
Tanaka, J ;
Ochi, T ;
Yoshikawa, H .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 59 (01) :110-117