Non-invasive mouse models of post-traumatic osteoarthritis

被引:123
作者
Christiansen, B. A. [1 ]
Guilak, F. [2 ]
Lockwood, K. A. [1 ]
Olson, S. A. [2 ]
Pitsillides, A. A. [3 ]
Sandell, L. J. [4 ]
Silva, M. J. [4 ]
van der Meulen, M. C. H. [5 ,6 ]
Haudenschild, D. R. [1 ]
机构
[1] Univ Calif Davis, Med Ctr, Dept Orthopaed Surg, Sacramento, CA 95817 USA
[2] Duke Univ, Med Ctr, Dept Orthopaed Surg, Durham, NC 27706 USA
[3] Royal Vet Coll London, Dept Comparat Biomed Sci, London, England
[4] Washington Univ, Dept Orthopaed Surg, St Louis, MO USA
[5] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[6] Cornell Univ, Sibley Sch Mech & Aerosp Engn, Ithaca, NY 14853 USA
基金
英国生物技术与生命科学研究理事会; 美国国家卫生研究院;
关键词
Post-traumatic osteoarthritis (PTOA); Mouse model; Articular cartilage; Knee injury; ANTERIOR CRUCIATE LIGAMENT; NECROSIS-FACTOR-ALPHA; MURINE KNEE-JOINT; ARTICULAR-CARTILAGE; IN-VIVO; INTRAARTICULAR FRACTURE; ANTIINFLAMMATORY DRUGS; OSTEOPHYTE FORMATION; BIOCHEMICAL-CHANGES; TIBIAL COMPRESSION;
D O I
10.1016/j.joca.2015.05.009
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
100224 [整形外科学];
摘要
Animal models of osteoarthritis (OA) are essential tools for investigating the development of the disease on a more rapid timeline than human OA. Mice are particularly useful due to the plethora of genetically modified or inbred mouse strains available. The majority of available mouse models of OA use a joint injury or other acute insult to initiate joint degeneration, representing post-traumatic osteoarthritis (PTOA). However, no consensus exists on which injury methods are most translatable to human OA. Currently, surgical injury methods are most commonly used for studies of OA in mice; however, these methods may have confounding effects due to the surgical/invasive injury procedure itself, rather than the targeted joint injury. Non-invasive injury methods avoid this complication by mechanically inducing a joint injury externally, without breaking the skin or disrupting the joint. In this regard, non-invasive injury models may be crucial for investigating early adaptive processes initiated at the time of injury, and may be more representative of human OA in which injury is induced mechanically. A small number of non-invasive mouse models of PTOA have been described within the last few years, including intra-articular fracture of tibial subchondral bone, cyclic tibial compression loading of articular cartilage, and anterior cruciate ligament (ACL) rupture via tibial compression overload. This review describes the methods used to induce joint injury in each of these non-invasive models, and presents the findings of studies utilizing these models. Altogether, these non-invasive mouse models represent a unique and important spectrum of animal models for studying different aspects of PTOA. (C) 2015 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1627 / 1638
页数:12
相关论文
共 99 条
[1]
Post-Traumatic Osteoarthritis: Improved Understanding and Opportunities for Early Intervention [J].
Anderson, Donald D. ;
Chubinskaya, Susan ;
Guilak, Farshid ;
Martin, James A. ;
Oegema, Theodore R. ;
Olson, Steven A. ;
Buckwaltert, Joseph A. .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2011, 29 (06) :802-809
[2]
Armstrong S J, 1993, Osteoarthritis Cartilage, V1, P89, DOI 10.1016/S1063-4584(05)80023-8
[3]
Arthritis Foundation, LEARN OST
[4]
Ex vivo characterization of articular cartilage and bone lesions in a rabbit ACL transection model of osteoarthritis using MRI and micro-CT [J].
Batiste, DL ;
Kirkley, A ;
Laverty, S ;
Thain, LMF ;
Spouge, AR ;
Holdsworth, DW .
OSTEOARTHRITIS AND CARTILAGE, 2004, 12 (12) :986-996
[5]
RAPID INDUCTION OF EARLY OSTEOARTHRITIC-LIKE LESIONS IN THE RABBIT KNEE BY CONTINUOUS INTRAARTICULAR INFUSION OF MAMMALIAN COLLAGENASE OR INTERLEUKIN-1 [J].
BORELLA, L ;
ENG, CP ;
DIJOSEPH, J ;
WELLS, C ;
WARD, J ;
CACCESE, R ;
BAEDER, WL .
AGENTS AND ACTIONS, 1991, 34 (1-2) :220-222
[6]
Long-term periarticular bone adaptation in a feline knee injury model for post-traumatic experimental osteoarthritis [J].
Boyd, SK ;
Müller, R ;
Leonard, T ;
Herzog, W .
OSTEOARTHRITIS AND CARTILAGE, 2005, 13 (03) :235-242
[7]
BRANDT KD, 1991, J RHEUMATOL, V18, P436
[8]
Aged Mice Have Enhanced Endocortical Response and Normal Periosteal Response Compared With Young-Adult Mice Following 1 Week of Axial Tibial Compression [J].
Brodt, Michael D. ;
Silva, Matthew J. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2010, 25 (09) :2006-2015
[9]
Posttraumatic osteoarthritis: A first estimate of incidence, prevalence, and burden of disease [J].
Brown, Thomas D. ;
Johnston, Richard C. ;
Saltzman, Charles L. ;
Marsh, J. Lawrence ;
Buckwalter, Joseph A. .
JOURNAL OF ORTHOPAEDIC TRAUMA, 2006, 20 (10) :739-744
[10]
Mechanical Injury Suppresses Autophagy Regulators and Pharmacologic Activation of Autophagy Results in Chondroprotection [J].
Carames, Beatriz ;
Taniguchi, Noboru ;
Seino, Daisuke ;
Blanco, Francisco J. ;
D'Lima, Darryl ;
Lotz, Martin .
ARTHRITIS AND RHEUMATISM, 2012, 64 (04) :1182-1192