Creation of myocardial tubes using cardiomyocyte sheets and an in vitro cell sheet-wrapping device

被引:86
作者
Kubo, Hirotsugu
Shimizu, Tatsuya
Yamato, Masayuki
Fujimoto, Tetsuo
Okano, Teruo
机构
[1] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo, Japan
[2] Shibaura Inst Technol, Grad Sch Engn, Med Res Inst, Tokyo 108, Japan
关键词
tissue engineering; myocardial tube; cell sheet; wrapping device; inner pressure;
D O I
10.1016/j.biomaterials.2007.04.016
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Regenerative medicine involving injection of isolated cells and transplantation of tissue-engineered myocardial patches, has received significant attention as an alternative method to repair damaged heart muscle. In the present study, as the next generation of myocardial tissue engineering we demonstrate the in vitro fabrication of pulsatile myocardial tubes using cell sheet engineering technologies. Three neonatal rat cardiomyocyte sheets, which were harvested from temperature-responsive culture dishes, were wrapped around fibrin tubes using a novel cell sheet-wrapping device. The tubular constructs demonstrated spontaneous, synchronized pulsation within 3 h after cell sheet wrapping. Contractile force measurements showed that the contractile force increased in accordance with both increasing rest length (Starling mechanism) and increasing extracellular Ca2+ concentration. Furthermore, the tissue-engineered myocardial tubes presented measurable inner pressure changes evoked by tube contraction (0.11 +/- 0.01 mmHg, max 0.15 mmHg, n = 5). Histological analyses revealed both well-differentiated sarcomeres and diffuse gap junctions within the myocardial tissues that resembled native cardiac muscle. These data indicate that tissue-engineered myocardial tubes have native heart-like structure and function. These new myocardial tissue constructs should be useful for future applications in physiological studies and pharmacological screening, and present a possible core technology for the creation of engineered tissues capable of independent cardiac assistance. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3508 / 3516
页数:9
相关论文
共 30 条
[1]
Cardiac muscle tissue engineering: toward an in vitro model for electrophysiological studies [J].
Bursac, N ;
Papadaki, M ;
Cohen, RJ ;
Schoen, FJ ;
Eisenberg, SR ;
Carrier, R ;
Vunjak-Novakovic, G ;
Freed, LE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1999, 277 (02) :H433-H444
[2]
Rebuilding broken hearts [J].
Cohen, S ;
Leor, J .
SCIENTIFIC AMERICAN, 2004, 291 (05) :44-51
[3]
Three-dimensional reconstitution of embryonic cardiomyocytes in a collagen matrix: a new heart muscle model system [J].
Eschenhagen, T ;
Fink, C ;
Remmers, U ;
Scholz, H ;
Wattchow, J ;
Weil, J ;
Zimmerman, W ;
Dohmen, HH ;
Schafer, H ;
Bishopric, N ;
Wakatsuki, T ;
Elson, EL .
FASEB JOURNAL, 1997, 11 (08) :683-694
[4]
Engineering myocardial tissue [J].
Eschenhagen, T ;
Zimmermann, WH .
CIRCULATION RESEARCH, 2005, 97 (12) :1220-1231
[5]
Novel 3D culture system for study of cardiac myocyte development [J].
Evans, HJ ;
Sweet, JK ;
Price, RL ;
Yost, M ;
Goodwin, RL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (02) :H570-H578
[6]
Chronic stretch of engineered heart tissue induces hypertrophy and functional improvement [J].
Fink, C ;
Ergün, S ;
Kralisch, D ;
Remmers, U ;
Weil, J ;
Eschenhagen, T .
FASEB JOURNAL, 2000, 14 (05) :669-679
[7]
Electrical coupling of cardiomyocyte sheets occurs rapidly via functional gap junction formation [J].
Haraguchi, Yuji ;
Shimizu, Tatsuya ;
Yamato, Masayuki ;
Kikuchi, Akihiko ;
Okano, Teruo .
BIOMATERIALS, 2006, 27 (27) :4765-4774
[8]
Silicon micromachining to tissue engineer branched vascular channels for liver fabrication [J].
Kaihara, S ;
Borenstein, J ;
Koka, R ;
Lalan, S ;
Ochoa, ER ;
Ravens, M ;
Pien, H ;
Cunningham, B ;
Vacanti, JP .
TISSUE ENGINEERING, 2000, 6 (02) :105-117
[9]
Kushida A, 1999, J BIOMED MATER RES, V45, P355, DOI 10.1002/(SICI)1097-4636(19990615)45:4<355::AID-JBM10>3.0.CO
[10]
2-7