Design of prevascularized three-dimensional cell-dense tissues using a cell sheet stacking manipulation technology

被引:236
作者
Sasagawa, Tadashi [1 ]
Shimizu, Tatsuya [1 ]
Sekiya, Sachiko [1 ]
Haraguchi, Yuji [1 ]
Yamato, Masayuki [1 ]
Sawa, Yoshiki [2 ]
Okano, Teruo [1 ]
机构
[1] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, TWIns, Shinjuku Ku, Tokyo 1628666, Japan
[2] Osaka Univ, Grad Sch Med, Dept Cardiovasc Surg, Osaka 5650871, Japan
关键词
Cell sheet; Endothelial cell; Co-culture; Prevascularization; Functional anastomosis; RESPONSIVE CULTURE DISHES; ENDOTHELIAL-CELLS; 2-DIMENSIONAL MANIPULATION; CARDIOMYOCYTE SHEETS; TEMPERATURE; SURFACES; COCULTURE; FABRICATION; DEFECTS; HARVEST;
D O I
10.1016/j.biomaterials.2009.11.036
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
To survive three-dimensional (3-D) cell-dense thick tissues after transplantation, the improvements of hypoxia, nutrient insufficiency, and accumulation of waste products are required. This study presents a strategy for the initiation of prevascular networks in a 3-D tissue construct by sandwiching endothelial cells between the cell sheets. For obtaining a stable stacked cell sheet construct, a sophisticated 3-D cell sheet manipulation system using temperature-responsive culture dishes and a cell sheet manipulator was developed. When sparsely cultured human umbilical vein endothelial cells (HUVECs) were sandwiched between two myoblast sheets, the inserted HUVECs sprouted and formed network structures in vitro. Additionally, when myoblast sheets and HUVECs were alternately sandwiched, endothelial cell connections through the layers and capillary-like structures were found in a five-layer construct. Moreover, the endothelial networks in the five-layer myoblast sheet construct were observed to connect to the host vessels after transplantation into the subcutaneous tissues of nude rats, resulted in a neovascularization that allow the graft to survive. These results indicated that the prevascularized myoblast sheet constructs could induce functional anastomosis. Consequently, our prevascularizing method using a cell sheet stacking manipulation technology provides a substantial advance for developing various types of three-dimensional tissues and contributes to regenerative medicine. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1646 / 1654
页数:9
相关论文
共 29 条
[1]   The arthroscopic implantation of autologous chondrocytes for the treatment of full-thickness cartilage defects of the knee joint [J].
Erggelet, C ;
Sittinger, M ;
Lahm, A .
ARTHROSCOPY-THE JOURNAL OF ARTHROSCOPIC AND RELATED SURGERY, 2003, 19 (01) :108-110
[2]   SELF-REGULATION OF GROWTH IN 3 DIMENSIONS [J].
FOLKMAN, J ;
HOCHBERG, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1973, 138 (04) :745-753
[3]   Patellofemoral full-thickness chondral defects treated with hyalograft-C - A clinical, arthroscopic, and histologic review [J].
Gobbi, Alberto ;
Kon, Elisaveta ;
Berruto, Massimo ;
Francisco, Ramces ;
Filardo, Giuseppe ;
Marcacci, Maurilio .
AMERICAN JOURNAL OF SPORTS MEDICINE, 2006, 34 (11) :1763-1773
[4]   Novel approach for achieving double-layered cell sheets co-culture: overlaying endothelial cell sheets onto monolayer hepatocytes utilizing temperature-responsive culture dishes [J].
Harimoto, M ;
Yamato, M ;
Hirose, M ;
Takahashi, C ;
Isoi, Y ;
Kikuchi, A ;
Okano, T .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 62 (03) :464-470
[5]   A thermoresponsive, microtextured substrate for cell sheet engineering with defined structural organization [J].
Isenberg, Brett C. ;
Tsuda, Yukiko ;
Williams, Corin ;
Shimizu, Tatsuya ;
Yamato, Masayuki ;
Okano, Teruo ;
Wong, Joyce Y. .
BIOMATERIALS, 2008, 29 (17) :2565-2572
[6]   Two-dimensional manipulation of confluently cultured vascular endothelial cells using temperature-responsive poly(N-isopropylacrylamide)-grafted surfaces [J].
Kikuchi, A ;
Okuhara, M ;
Karikusa, F ;
Sakurai, Y ;
Okano, T .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1998, 9 (12) :1331-1348
[7]  
Kushida A, 1999, J BIOMED MATER RES, V45, P355, DOI 10.1002/(SICI)1097-4636(19990615)45:4<355::AID-JBM10>3.0.CO
[8]  
2-7
[9]  
Kushida A, 2001, J BIOMED MATER RES, V54, P37, DOI 10.1002/1097-4636(200101)54:1<37::AID-JBM5>3.0.CO
[10]  
2-7