Factors regulating osteoclast formation in human tissues adjacent to peri-implant bone loss:: expression of receptor activator NFκB, RANK ligand and osteoprotegerin

被引:122
作者
Crotti, TN
Smith, MD
Findlay, DM
Zreiqat, H
Ahern, MJ
Weedon, H
Hatzinikolous, G
Capone, M
Holding, C
Haynes, DR [1 ]
机构
[1] Univ Adelaide, Div Hlth Sci, Dept Pathol, Adelaide, SA 5005, Australia
[2] Flinders Med Ctr, Dept Med, Adelaide, SA, Australia
[3] Repatriat Gen Hosp, Adelaide, SA, Australia
[4] Univ Adelaide, Dept Orthopaed & Trauma, Adelaide, SA, Australia
[5] Univ New S Wales, Sch Pathol, Kensington, NSW 2033, Australia
基金
英国医学研究理事会;
关键词
osteolysis; joint replacement; pathology; immunochemistry; in situ hybridization;
D O I
10.1016/S0142-9612(03)00556-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Aseptic bone loss adjacent to orthopedic joint implants is a common cause of joint implant failure in humans. This study investigates the expression of key regulators of osteoclast formation, receptor activator NFkappaB (RANK), Receptor activator of NFkappaB ligand (RANKL) and osteoprotegerin (OPG), in the peri-implant tissues of patients with osteolysis compared with levels in synovial tissues from osteoarthritic and healthy subjects. Immunohistochemical studies demonstrated that significantly higher levels of RANKL protein (p<0.05) were found in the peri-implant tissues of patients with implant failure than in similar tissues from osteoarthritic and healthy subjects. In contrast, OPG protein levels were similar in all tissues. RANKL, expressed as mRNA and protein, was predominantly associated with cells containing wear particles. Dual labeling studies showed that the cells expressing RANKL protein were macrophages. In situ hybridization studies confirmed that mRNA encoding for these proteins is also expressed by cells in the peri-implant tissues. In addition, RANK mRNA was expressed in cells that contained wear particles. These findings show that abnormally high levels of RANKL are expressed in peri-implant tissues of patients with prosthetic loosening and that these abnormal levels of RANKL may significantly contribute to aseptic implant loosening. (c) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:565 / 573
页数:9
相关论文
共 44 条
[11]   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
[12]   THE SYNOVIAL-LIKE MEMBRANE AT THE BONE-CEMENT INTERFACE IN LOOSE TOTAL HIP REPLACEMENTS AND ITS PROPOSED ROLE IN BONE LYSIS [J].
GOLDRING, SR ;
SCHILLER, AL ;
ROELKE, M ;
ROURKE, CM ;
ONEILL, DA ;
HARRIS, WH .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1983, 65 (05) :575-584
[13]   Cellular profile and cytokine production at prosthetic interfaces - Study of tissues retrieved from revised hip and knee replacements [J].
Goodman, SB ;
Huie, P ;
Song, Y ;
Schurman, D ;
Maloney, W ;
Woolson, S ;
Sibley, R .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1998, 80B (03) :531-539
[14]  
Gravallese EM, 2000, ARTHRITIS RHEUM, V43, P250, DOI 10.1002/1529-0131(200002)43:2<250::AID-ANR3>3.0.CO
[15]  
2-P
[16]   Osteoprotegerin and receptor activator of nuclear factor kappaB ligand (RANKL) regulate osteoclast formation by cells in the human rheumatoid arthritic joint [J].
Haynes, DR ;
Crotti, TN ;
Loric, M ;
Bain, GI ;
Atkins, GJ ;
Findlay, DM .
RHEUMATOLOGY, 2001, 40 (06) :623-630
[17]   The osteoclastogenic molecules RANKL and RANK are associated with periprosthetic osteolysis [J].
Haynes, DR ;
Crotti, TN ;
Potter, AE ;
Loric, M ;
Atkins, GJ ;
Howie, DW ;
Findlay, DM .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2001, 83B (06) :902-911
[18]   Bidirectional signaling between stromal and hemopoietic cells regulates interleukin-1 expression during human osteoclast formation [J].
Haynes, DR ;
Atkins, GJ ;
Loric, M ;
Crotti, TN ;
Geary, SM ;
Findlay, DM .
BONE, 1999, 25 (03) :269-278
[19]  
HAYNES DR, 2003, RHEUMATOLOGY, V43, P1
[20]   Effect of osteoprotegerin and osteoprotegerin ligand on osteoclast formation by arthroplasty membrane derived macrophages [J].
Itonaga, I ;
Sabokbar, A ;
Murray, DW ;
Athanasou, NA .
ANNALS OF THE RHEUMATIC DISEASES, 2000, 59 (01) :26-31