45 In Vivo Models for Articular Cartilage Repair



10.1055/b-0035-122045

45 In Vivo Models for Articular Cartilage Repair

Paul Hindle

The translation of basic science research requires rigorous investigation prior to human clinical trials. An important step in this process is the use of in vivo animal models. 1, 2, 3, 4 They allow the efficacy and safety to be tested in a biological and mechanical environment that aims to protect patients from unsafe drugs or procedures.


The main areas that can be investigated include:




  • Foreign-body reactions to new materials (biocompatibility)



  • Effects of materials on healing



  • Immunological response to cells, autologous and allogeneic



  • Effect of growth factors, drugs and other compounds



  • Safety and efficacy of new treatments



  • Mechanical response to nonbiological implants



  • Biological pathways assessment by up- and downregulation of genetic expression



  • Mechanical loading of healing tissues


Despite the use of in vitro methods and the promise of technologies, such as induced pluripotent stem cells, there is not a sufficient alternative to in vivo studies at this time. The use of animals unable to consent raises ethical and social concerns that vary from country to country. In the United Kingdom, animal research is legislated by the Animals (Scientific Procedures) Act 1986 and regulated by the Home Office.


Before any research is undertaken, the question and hypothesis need to be clearly defined. This allows three vital questions to be answered. The first is “Has this work been undertaken before?” A thorough review of the literature is mandatory to ensure that animals are not used superfluously; this includes the foreign literature where practicable. The second question is “Can this question be answered using an in vitro laboratory technique without the use of live animals?” For short-term experiments (up to 3 to 4 weeks), sometimes cadaveric tissue will suffice as cells will function postmortem and can provide valid results in appropriate experiments. The third is “Is my experimental model robust enough to provide sufficient data to justify the use of live animals?” There is no excuse for poorly planned experiments wasting animals’ lives to no scientific or clinical benefit.


Researchers planning on undertaking animal research need to be fully aware of and trained and supported by appropriate veterinary staff to ensure that disruption to the welfare of the animals is reduced as much as possible. The relative cost and time frame compared to in vitro work needs to be considered.



45.1 Animal Models


To determine the most appropriate animal to use, a number of key factors need to be determined. The first is the model of cartilage repair to be used. The options include heterotopic, cartilage defect, and arthritic or articular fracture, and are described in greater detail below.


After promising in vitro results, a heterotopic model of chondrogenesis should be considered. This would typically be subcutaneous, intramuscular, or intraperitoneal. The rat xiphoid has also been proposed as a potential nonjoint model for cartilage regeneration strategies. Animals used for these studies include nude mice, syngenic mice, rats, and rabbits. Cells can be implanted directly, injected, or introduced within a diffusion chamber. These studies allow researchers to look at the biological effect of the cells being in vivo without the need to use an articular cartilage defect model.


There are two types of cartilage defect models to be considered, partial or full thickness, which relate to whether or not the subchondral plate is breached. 5, 6 The choice depends on the hypothesis to be tested. Breaching the subchondral bone when not intended will release bone marrow (including clotting factors and stem cells), which can invalidate the technique being investigated.


Generalized arthritis can be induced by a number of methods. The most common of these include mechanical resection of ligaments, including the anterior cruciate or the cranial cruciate ligament (the Pond-Nuki model), or menisci, which is resection of the medial meniscus inducing medial compartment arthritis. Other possible methods include treatment of spontaneous disease, obesity models, hormone deficiency (ovariectomy), chemical damage (direct cartilage degradation and indirect metabolism inhibition), limb immobilization, hypermotility, and scoring grooves in the cartilage.


Rodent models have also been used in a model of articular fracture healing.



45.2 Animal Selection


Animals are usually categorized into small or large models. Small animals include mice, rats, rabbits, and guinea pigs, and large animals include dogs, pigs, minipigs, sheep, goats, and horses. The International Society for Cartilage Repair recommends that while small animal models are useful for initial studies and proof-of-concept work, a large animal study is required for pivotal studies.4


Species selection will be affected by the type of model to be used; heterotopic models typically use small animal models. Cartilage defect and arthritis models can use small and large animal models. Small animals are more appropriate for proof-of-concept work or looking at the effect of drugs, compounds, or alterations in genetic expression. Surgical techniques are better assessed with a large animal model.


The advantage of using small animals such as rodents and rabbits includes ease of use, reduced cost, easier husbandry, and the ability to view the entire joint on one histological slide. Their disadvantages include their relatively smaller joints, thinner cartilage, and problems with postoperative care.


Large animals also have their associated benefits and problems. The use of dogs is socially unacceptable in the United Kingdom due to their status as companion animals. Despite having thicker cartilage, pigs are hard to work with and seldom used as the minipig is easier to work with. Goats have been widely used due to their anatomical shape and cartilage thickness; they are, however, hard to work with and may have been affected with prion disease causing early arthritis leading to early termination of experiments. The sheep is easy to handle and relatively amenable. They have thinner cartilage than some of the other animals but have been successfully used for autologous chondrocyte implantation despite this. Horses have the thickest cartilage and the largest joints, making them the best comparison to human joints, 7 and they themselves have problems with osteochondral disease. Horses are, however, very expensive if large numbers are required and they need to be kept for a long time. There are also similar issues as for the dog due to their status as companion animals. Injured horses that are destined for euthanasia may be considered more appropriate for studies of treatment.


As well as the type of model to be used, species selection will be determined by a number of other factors. The literature will suggest if one particular species has been used for a particular area; if this is the case, using the same species will allow results to be comparable. Local expertise, animal availability, and housing facilities also have to be considered. Other factors to be considered include cartilage thickness, skeletal maturity, and the differing in vitro biology of chondrocytes if they are to be used in the repair.


Cartilage thickness varies from study to study. Simon 8 looked at the variation between species and joint (Table 45.1) and observed the stress across the joint; he also related the thickness to the elasticity of the cartilage. 9 Much more recently, Frisbie et al 10 compared the thickness between humans and varying species but also compared various sites within the stifle joint (Table 45.2).
































































Table 45.2 Interspecies and Intrajoint Variation of the Articular Cartilage Thickness of the Stifle/Knee Joint10

Species/Location


PMT


LT


DMT


PMC


DMC


Dog


524 ± 30


530 ± 30


530 ± 30


771 ± 30


731 ± 30


Equine


1832 ± 30


2162 ± 30


1761 ± 30


2215 ± 30


2203 ± 30


Goat


799 ± 30


699 ± 30


786 ± 30


1279 ± 30


1510 ± 30


Human


2596 ± 43


2877 ± 33


2461 ± 43


2411 ± 30


2523 ± 30


Rabbit


221 ± 30


314 ± 30


306 ± 30


341 ± 30


271 ± 30


Sheep


559 ± 30


707 ± 30


559 ± 30


542 ± 30


609 ± 30


[Mean ± SEM in micrometers for the sum of calcified cartilage and the noncalcified cartilage in each location for each species.] Abbreviations: SEM, standard error of the mean; PMT, proximal medial trochlear; LT, lateral trochlear; DMT, distal medial trochlear; PMC, proximal medial condyle; DMC, distal medial condyle.































































Table 45.1 Interspecies and Joint Variation in Articular Cartilage Thickness8

Average maximum cartilage thickness (mm)


Species


Hip


Knee


Patella


Ankle


Shoulder


Elbow


Cow


2.49


3.17


3.13


1.43


3.03


1.44


Sheep


1.36


1.68


1.65


0.27


1.39


0.62


Dog


1.19


1.30


1.10


0.06


0.98


0.76


Rat


0.091


0.165


0.060


0.038


0.188


0.095


Mouse


0.053


0.030


0.024


0.023


0.038


0.034


The skeletal maturity of the animals to be used also has to be considered. Immature cartilage in skeletally immature animals has a greater potential to heal and therefore does not represent the condition found in human adults. The age of sheep has been found to affect the behavior of cultured chondrocytes.


Each species has its relative benefits and problems, and no one species is ideal for all stages of research. Our opinion is that mice may be most appropriate for heterotopic models, rabbits for proof-of-concept work, and sheep for large animal studies.

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Jun 10, 2020 | Posted by in ORTHOPEDIC | Comments Off on 45 In Vivo Models for Articular Cartilage Repair

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