Chitosan-glycerol phosphate/blood implants increase cell recruitment, transient vascularization and subchondral bone remodeling in drilled cartilage defects

被引:136
作者
Chevrier, A.
Hoemann, C. D.
Sun, J.
Buschmann, M. D.
机构
[1] Ecole Polytech, Dept Chem Engn, Montreal, PQ H3C 3A7, Canada
[2] Biosyntech Canada Inc, Laval, PQ, Canada
基金
加拿大健康研究院;
关键词
chitosan; cartilage; cartilage repair; bone repair; biodegradation; biocompatibility; chemotaxis; angiogenesis;
D O I
10.1016/j.joca.2006.08.007
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: Marrow-stimulation techniques are used by surgeons to repair cartilage lesions although consistent regeneration of hyaline cartilage is rare. We have shown previously that autologous blood can be mixed with a polymer solution containing chitosan in a glycerol phosphate (GP) buffer (chitosan-GP), and that implantation of this polymer/blood composite onto marrow-stimulated chondral defects in rabbit and sheep leads to the synthesis of more chondral repair tissue with greater hyaline character compared to marrow-stimulation alone. In the current study, we examined the modulation of cell recruitment and repair tissue characteristics at early post-surgical time points (from day 1 to 56) in a rabbit model to elucidate potential mechanisms behind this improved repair outcome. Design: Thirty-three skeletally mature New Zealand White rabbits underwent bilateral arthrotomies, with each trochlea receiving a cartilage defect (3.5 mm x 4.5 mm) bearing four microdrill holes (0.9 mm diameter, similar to 4 mm deep) into the subchondral bone. One defect per rabbit was treated with a chitosan-GP/blood implant, while the other defect was left as a microdrilled control. Repair tissues were stained by histochemistry, for collagen types I, II, and X by immunohistochemistry and analyzed using quantitative stereological tools. Results: Histological analyses demonstrated that control defects followed a typical healing sequence observed previously in marrow-stimulation animal models while chitosan-GP/blood implants led to three significant modifications in the healing sequence at early stages: (1) increased inflammatory and marrow-derived stromal cell recruitment to the microdrill holes, (2) increased vascularization of the provisional repair tissue in the microdrill holes, and (3) increased intramembranous bone formation and subchondral bone remodeling (BR). Conclusions: These results suggest that the greater levels of provisional tissue vascularization and BR activity are main factors supporting improved cartilage repair when chitosan-GP/blood implants are applied to marrow-stimulated cartilage lesions. (C) 2006 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:316 / 327
页数:12
相关论文
共 43 条
  • [1] ARNOCZKY SP, 1996, OPERATIVE ARTHROSCOP, P211
  • [2] Effect of cultured autologous chondrocytes on repair of chondral defects in a canine model
    Breinan, HA
    Minas, T
    Hsu, HP
    Nehrer, S
    Sledge, CB
    Spector, M
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1997, 79A (10) : 1439 - 1451
  • [3] Novel injectable neutral solutions of chitosan form biodegradable gels in situ
    Chenite, A
    Chaput, C
    Wang, D
    Combes, C
    Buschmann, MD
    Hoemann, CD
    Leroux, JC
    Atkinson, BL
    Binette, F
    Selmani, A
    [J]. BIOMATERIALS, 2000, 21 (21) : 2155 - 2161
  • [4] Chevrier A, 2005, J HISTOTECHNOL, V28, P165
  • [5] Vascular proliferation and blood supply during distraction osteogenesis: A scanning electron microscopic observation
    Choi, IH
    Ahn, JH
    Chung, CY
    Cho, TJ
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 2000, 18 (05) : 698 - 705
  • [6] Chitosan enhances platelet adhesion and aggregation
    Chou, TC
    Fu, E
    Wu, CJ
    Yeh, JH
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 302 (03) : 480 - 483
  • [7] Vascular cell responses to polysaccharide materials: in vitro and in vivo evaluations
    Chupa, JM
    Foster, AM
    Sumner, SR
    Madihally, SV
    Matthew, HWT
    [J]. BIOMATERIALS, 2000, 21 (22) : 2315 - 2322
  • [8] CLARK RAF, 1996, MOL CELLULAR BIOL WO, P1
  • [9] COLOTTA F, 1992, BLOOD, V80, P2012
  • [10] FILION D, UNPUB BIOMACROMOLECU