Biodegradable polymer with collagen microsponge serves as a new bioengineered cardiovascular prosthesis

被引:61
作者
Iwai, S
Sawa, Y
Ichikawa, H
Taketani, S
Uchimura, E
Chen, GP
Hara, M
Miyake, J
Matsuda, H
机构
[1] Osaka Univ, Grad Sch Med, Div Cardiovasc Surg, Dept Surg, Osaka, Japan
[2] Osaka Prefecture Univ, Dept Appl Biosci, Res Inst Adv Sci & Technol, Osaka, Japan
关键词
D O I
10.1016/j.jtcvs.2004.04.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Biodegradable materials with autologous cell seeding have attracted much interest as potential cardiovascular grafts. However, pretreatment of these materials requires a complicated and invasive procedure that carries the risk of infection. To avoid these problems, we sought to develop a biodegradable graft material containing collagen microsponge that would permit the regeneration of autologous vessel tissue. The ability of this material to accelerate in situ cellularization with autologous endothelial and smooth muscle cells was tested with and without precellularization. Methods: Poly(lactic-co-glycolic acid) as a biodegradable scaffold was compounded with collagen microsponge to form a vascular patch material. These poly(lactic-co-glycolic acid)-collagen patches with (n = 10) or without (n = 10) autologous vessel cellularization were used to patch the canine pulmonary artery trunk. Histologic and biochemical assessments were performed 2 and 6 months after the implantation. Results: There was no thrombus formation in either group, and the poly(lactic-co-glycolic acid) scaffold was almost completely absorbed in both groups. Histologic results showed the formation of an endothelial cell monolayer, a parallel alignment of smooth muscle cells, and reconstructed vessel wall with elastin and collagen fibers. The cellular and extracellular components in the patch had increased to levels similar to those in native tissue at 6 months. Conclusions: The poly(lactic-co-glycolic acid)-collagen microsponge patch with and without precellularization showed good histologic findings and durability. This patch shows promise as a bioengineered material for promoting in situ cellularization and the regeneration of autologous tissue in cardiovascular surgery.
引用
收藏
页码:472 / 479
页数:8
相关论文
共 25 条
  • [1] Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization
    Asahara, T
    Masuda, H
    Takahashi, T
    Kalka, C
    Pastore, C
    Silver, M
    Kearne, M
    Magner, M
    Isner, JM
    [J]. CIRCULATION RESEARCH, 1999, 85 (03) : 221 - 228
  • [2] Redifferentiation of dedifferentiated bovine chondrocytes when cultured in vitro in a PLGA-collagen hybrid mesh
    Chen, G
    Sato, T
    Ushida, T
    Hirochika, R
    Tateishi, T
    [J]. FEBS LETTERS, 2003, 542 (1-3) : 95 - 99
  • [3] Chen GP, 2000, J BIOMED MATER RES, V51, P273, DOI 10.1002/(SICI)1097-4636(200008)51:2<273::AID-JBM16>3.0.CO
  • [4] 2-O
  • [5] Circulating bone marrow cells can contribute to neointimal formation
    Han, CL
    Campbell, GR
    Campbell, JH
    [J]. JOURNAL OF VASCULAR RESEARCH, 2001, 38 (02) : 113 - 119
  • [6] DIFFERENTIAL-EFFECTS OF LAMININ, INTACT TYPE-IV COLLAGEN, AND SPECIFIC DOMAINS OF TYPE-IV COLLAGEN ON ENDOTHELIAL-CELL ADHESION AND MIGRATION
    HERBST, TJ
    MCCARTHY, JB
    TSILIBARY, EC
    FURCHT, LT
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 106 (04) : 1365 - 1373
  • [7] Restoration to a quiescent and contractile phenotype from a proliferative phenotype of myofibroblast-like human aortic smooth muscle cells by culture on type IV collagen gels
    Hirose, M
    Kosugi, H
    Nakazato, K
    Hayashi, T
    [J]. JOURNAL OF BIOCHEMISTRY, 1999, 125 (06) : 991 - 1000
  • [8] Tissue engineering of functional trileaflet heart valves from human marrow stromal cells
    Hoerstrup, SP
    Kadner, A
    Melnitchouk, S
    Trojan, A
    Eid, K
    Tracy, J
    Sodian, R
    Visjager, JF
    Kolb, SA
    Grunenfelder, J
    Zund, G
    Turina, MI
    [J]. CIRCULATION, 2002, 106 (13) : I143 - I150
  • [9] Delivery of a growth factor fusion protein having collagen-binding activity to wound tissues
    Ishikawa, T
    Terai, H
    Yamamoto, T
    Harada, K
    Kitajima, T
    [J]. ARTIFICIAL ORGANS, 2003, 27 (02) : 147 - 154
  • [10] Kim BS, 1998, BIOTECHNOL BIOENG, V57, P46