Animal Models of Temporomandibular Joint Disorders: Implications for Tissue Engineering Approaches

被引:27
作者
Almarza, Alejandro J. [1 ]
Hagandora, Catherine K. [1 ]
Henderson, Sarah E. [1 ]
机构
[1] Univ Pittsburgh, Dept Oral Biol, McGowan Inst Regenerat Med, Ctr Craniofacial Regenerat,Dept Bioengn, Pittsburgh, PA 15260 USA
关键词
Temporomandibular joint; Disc; Condyle; Animal model; Temporomandibular joint disorder; INFLAMMATORY IRRITANT APPLICATION; EXPERIMENTAL DISK PERFORATION; ANTIGEN-INDUCED ARTHRITIS; ARTICULAR SOFT-TISSUE; GROWTH-FACTORS; BRAIN-STEM; TMJ PAIN; RABBIT; RATS; CONDYLECTOMY;
D O I
10.1007/s10439-011-0364-8
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Animal models for temporomandibular joint disorder (TMD) or degradation are necessary for assessing the value of current and future tissue engineering therapies. After reviewing the literature, it is quite apparent that most TMD animal studies can be categorized into chemical approaches or surgical/mechanical approaches. Overall, it was found that the top five cited manuscripts for all chemical models were cited by almost 40% more manuscripts than the top five manuscripts for surgical/mechanical models. It is clear that the chemical approaches have focused on the inflammatory aspect of TMDs and its relationship to pain. However, chemical irritants must be tested in larger animal models, and the effect of short-term inflammation on the mechanical properties of the fibrocartilage must be examined. Nevertheless, therapeutic approaches aimed at reducing or controlling inflammation could use the established chemical methods. Surgical/mechanical methods can be used as negative controls for first generation TMJ tissue engineering approaches when the therapy is applied immediately after injury. Next generation tissue engineering approaches will require testing on tissues degenerated for a few months after the surgical/mechanical methods, with enhanced functional assessment techniques.
引用
收藏
页码:2479 / 2490
页数:12
相关论文
共 86 条
[1]
HISTOPATHOLOGICAL CHANGES IN RABBIT CRANIOMANDIBULAR JOINT ASSOCIATED WITH EXPERIMENTALLY-INDUCED ANTERIOR DISK DISPLACEMENT (ADD) [J].
ALI, AM ;
SHARAWY, MM .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1994, 23 (08) :364-374
[2]
Scaffold and growth factor selection in temporomandibular joint disc engineering [J].
Allen, K. D. ;
Athanasiou, K. A. .
JOURNAL OF DENTAL RESEARCH, 2008, 87 (02) :180-185
[3]
Allen K D, 2006, Orthod Craniofac Res, V9, P143, DOI 10.1111/j.1601-6343.2006.00370.x
[4]
A surface-regional and freeze-thaw characterization of the porcine temporomandibular joint disc [J].
Allen, KD ;
Athanasiou, KA .
ANNALS OF BIOMEDICAL ENGINEERING, 2005, 33 (07) :951-962
[5]
The effects of protein-coated surfaces on passaged porcine TMJ disc cells [J].
Allen, Kyle D. ;
Erickson, Kathryn ;
Athanasiou, Kyriacos A. .
ARCHIVES OF ORAL BIOLOGY, 2008, 53 (01) :53-59
[6]
Effect of passage and topography on gene expression of temporomandibular joint disc cells [J].
Allen, Kyle D. ;
Athanasiou, Kyriacos A. .
TISSUE ENGINEERING, 2007, 13 (01) :101-110
[7]
Evaluation of three growth factors in combinations of two for temporomandibular joint disc tissue engineering [J].
Almarza, AJ ;
Athanasiou, KA .
ARCHIVES OF ORAL BIOLOGY, 2006, 51 (03) :215-221
[8]
Effects of initial cell seeding density for the tissue engineering of the temporomandibular joint disc [J].
Almarza, AJ ;
Athanasiou, KA .
ANNALS OF BIOMEDICAL ENGINEERING, 2005, 33 (07) :943-950
[9]
Seeding techniques and scaffolding choice for tissue engineering of the temporomandibular joint disk [J].
Almarza, AJ ;
Athanasiou, KA .
TISSUE ENGINEERING, 2004, 10 (11-12) :1787-1795
[10]
Effects of hydrostatic pressure on TMJ disc cells [J].
Almarza, Alejandro J. ;
Athanasiou, Kyriacos A. .
TISSUE ENGINEERING, 2006, 12 (05) :1285-1294