Murine model of prosthesis failure for the long-term study of aseptic loosening

被引:65
作者
Yang, Shang-You
Yu, Haiying
Gong, Weiming
Wu, Bin
Mayton, Lois
Costello, Richard
Wooley, Paul H.
机构
[1] Wayne State Univ, Dept Orthopaed Surg, Detroit, MI 48201 USA
[2] John D Dingell VA Med Ctr, Detroit, MI 48201 USA
[3] Jinan Cent Hosp, Dept Orthopaed Surg, Shandong, Peoples R China
关键词
animal model; aseptic loosening; wear debris; pullout test; gene therapy;
D O I
10.1002/jor.20342
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
We examined a novel mouse model of wear debris-induced prosthesis instability and osteolysis, and its application for the evaluation of therapy. A stainless steel or titanium-alloy pin was implanted into the proximal tibia to form a contiguous surface with the articular cartilage. In some mice, titanium particles were injected into the tibial canal during the surgery, followed by monthly intraarticular injection. MicroCT scans revealed that the implants without particle challenge were stable without bone mineral density changes for 6 months. Histological analysis showed new bone formation around the implant at 6 weeks postsurgery. Periprosthetic soft tissue with inflammatory cells was a ubiquitous finding at the interface between the implant and surrounding bone in samples exposed to titanium particles, and expression of IL-1 beta, TNF alpha, and CD68 was common in these joints. Pullout tests indicated that an average 5N load was required to pull out stable implants from surrounding bone. However, particle stimulation dramatically reduced the pullout force to less than 0.4 N. The feasibility of in vivo gene transfer on this model was confirmed by X-gal staining of synovial membrane and periprosthetic tissue after injection of AAV-LacZ in the prosthetic joint. This murine model of weight-bearing knee prosthesis provides an economical, reproducible, and easily obtained means to study joint arthroplasty failure. The ability to evaluate the biomechanical properties of the prosthetic joint, in addition to histological and biochemical examination, results in a useful model to investigate many of the properties of prosthetic joint components during the response to debris-associated osteolysis. (c) 2007 Ortbopaedic Research Society.
引用
收藏
页码:603 / 611
页数:9
相关论文
共 36 条
[1]   The effects of particulate polyethylene at a weight-bearing bone-implant interface - A study in rats [J].
Allen, M ;
Brett, F ;
Millett, P ;
Rushton, N .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1996, 78B (01) :32-37
[2]   The pathology of total joint arthroplasty - II. Mechanisms of implant failure [J].
Bauer, TW ;
Schils, J .
SKELETAL RADIOLOGY, 1999, 28 (09) :483-497
[3]   CELLULAR PROLIFERATION AND CYTOKINE RESPONSES TO POLYMETHYLMETHACRYLATE PARTICLES IN PATIENTS WITH A CEMENTED TOTAL JOINT ARTHROPLASTY [J].
CHADHA, HS ;
WOOLEY, PH ;
SUD, S ;
FITZGERALD, RH .
INFLAMMATION RESEARCH, 1995, 44 (04) :145-151
[4]   Significance of peak value and duration of the interfacial shear load in evaluation of the bone-implant interface [J].
Chang, YS ;
Kobayashi, M ;
Li, ZL ;
Oka, M ;
Nakamura, T .
CLINICAL BIOMECHANICS, 2003, 18 (08) :773-779
[5]  
CHIBA J, 1994, CLIN ORTHOP RELAT R, V300, P304
[6]  
DOWD JE, 1995, CLIN ORTHOP RELAT R, P106
[7]   Biological fixation of hydroxyapatite-coated versus grit-blasted titanium hip stems: a canine study [J].
Eckardt, A ;
Aberman, HM ;
Cantwell, HD ;
Heine, J .
ARCHIVES OF ORTHOPAEDIC AND TRAUMA SURGERY, 2003, 123 (01) :28-35
[8]   An animal model for interface tissue formation in cemented hip replacements [J].
El-Warrak, AO ;
Olmstead, M ;
Apelt, D ;
Deiss, F ;
Noetzli, H ;
Zlinsky, K ;
Hilbe, M ;
Bertschar-Wolfsberger, R ;
Johnson, AL ;
Auer, J ;
Von Rechenberg, B .
VETERINARY SURGERY, 2004, 33 (05) :495-504
[9]  
Friedman R J, 1994, Instr Course Lect, V43, P233
[10]   Efficacy of ex vivo OPG gene therapy in preventing wear debris induced osteolysis [J].
Goater, JJ ;
O'Keefe, RJ ;
Rosier, RN ;
Puzas, JE ;
Schwarz, EM .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (02) :169-173