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Journal of Biomedicine and Biotechnology
Volume 2012 (2012), Article ID 201689, 4 pages
Cytokines and VEGF Induction in Orthodontic Movement in Animal Models
1Department of General Pathology, Second University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy
2Department of Oral Pathology, Orthodontics and Oral Surgery, Institute of Biochemistry, Second University of Naples, Via L. De Crecchio 6, 80138 Naples, Italy
3INT-CROM, “Pascale Foundation” National Cancer Institute - Cancer Research Center, Via Ammiraglio Bianco, 83013 Mercogliano, Italy
4Department of Cellular and Molecular Biology and Pathology, Faculty of Medicine of Naples, University of Naples “Federico II,” Via Pansini 5, 80131 Naples, Italy
5Department of Experimental Medicine, Second University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy
6Department of Oral and Maxillofacial Sciences, University of Rome “La Sapienza”, Viale Regina Elena 287/A, 00161 Rome, Italy
Received 29 December 2011; Revised 13 March 2012; Accepted 14 March 2012
Academic Editor: Monica Fedele
Copyright © 2012 M. Di Domenico et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Orthodontics is a branch of dentistry that aims at the resolution of dental malocclusions. The specialist carries out the treatment using intraoral or extraoral orthodontic appliances that require forces of a given load level to obtain a tooth movement in a certain direction in dental arches. Orthodontic tooth movement is dependent on efficient remodeling of periodontal ligament and alveolar bone, correlated with several biological and mechanical responses of the tissues surrounding the teeth. A periodontal ligament placed under pressure will result in bone resorption whereas a periodontal ligament under tension results in bone formation. In the primary stage of the application of orthodontic forces, an acute inflammation occurs in periodontium. Several proinflammatory cytokines are produced by immune-competent cells migrating by means of dilated capillaries. In this paper we summarize, also through the utilization of animal models, the role of some of these molecules, namely, interleukin-1β and vascular endothelial growth factor, that are some proliferation markers of osteoclasts and osteoblasts, and the macrophage colony stimulating factor.
1. Orthodontic Movement and Inflammation
Orthodontic movement is correlated with an inflammatory process, that, in concert with the mechanical responses of periodontal and oral tissues, is essential for achieving tooth movement clinically. Early effects of orthodontic forces are of physical  and biological nature, and they involve extracellular matrix and cells of the alveolar bone, periodontal ligament, blood vessels, and neural elements. As consequence, many changes occur in these structures and various molecules are produced or inducted, as well as cytokines, growth factors, colony-stimulating factors, and neurotransmitters . The first stages before the orthodontic force application are characterized by an acute inflammatory response. In the periodontium this process involves the vasodilatation of capillaries which allows the migration of leucocytes in the periodontal tissue, where they are induced by biochemical signals to synthesize and to secrete several proinflammatory cytokines and chemokines, growth factors and enzymes.
Orthodontic appliances impose forces on the teeth with a predetermined direction, and tooth movement occurs through different phases. The biological responses of hard tissue to mechanical loadings around the tooth are different between a tension area and a compression area (Figure 1). Mechanical forces are transduced to the cells triggering the biologic response by means of an aseptic transitory inflammatory process that involves several inflammatory mediators. This succession of local events is the base for achieving the remodeling of the parodontium, so to allow the tooth movement .
The following paragraphs of the paper are intended to focus on the role of various chemical and cellular factors primarily present after the application of orthodontic forces.
The goal of this paper is to provide to orthodontic clinicians and educators some basic information and the summary of some updated studies about the correlation between tooth movement and inflammatory process. Understanding of these molecular phenomena is crucial to share the notion that orthodontic tooth movement is “the biologic response to interference in the physiologic equilibrium of the dentofacial complex by an externally applied force” .
1.1. Interleukine-1β Induction at Primary Stage of Orthodontic Tooth Movement
Cytokine expression in the rat periodontal ligament at the initial stage of orthodontic tooth movement has been investigated to evaluate the change of periodontal ligament. Interleukin (IL)-1β is one of the most abundant cytokines in the periodontal environment during the initial stage of orthodontic tooth movement because of its direct implications in alveolar bone resorption induced in the pressure side by mechanical loading .
IL-1β takes part in the survival, fusion, and activation of osteoclasts and exerts an important role since the amount of tooth movement correlates with the efficiency of bone remodeling in the alveolar process . Higher levels of expression of inflammatory cytokines and of their respective receptors had been shown after an inducted inflammatory process by perforating the buccal cortical plate of orthodontically treated rats. The concentration of IL-1β mRNA in the rats’ periodontal ligament is increased within 3 h after orthodontic force loading, particularly on pressure side . The soft tissues surrounding the teeth are involved in orthodontic tooth shift such as the hard tissues, periodontal ligament, and alveolar bone, and changes in gingival contour always follow tooth movement. After the application of mechanical loadings, IL-1β mRNA in pressure side gingival is significantly increased in a rat model under orthodontic treatment .
IL-1β can bind two types of receptors, IL-1RI and IL-1RII . Only the former is examined in this context [10, 11] since the latter acts only as a “decoy” target for the cytokine. The particular function as proinflammatory cytokine of IL-1β has been demonstrated by the administration of exogenous interleukin (IL)-1 receptor antagonist (IL-1Ra) in mice undergoing orthodontic treatment . The level of IL-1β decreased by 66% in mice treated with IL-Ra therapy, and this associated with a reduction of the number of osteoclasts in the pressure side of periodontal tissues after histological characterization, and with a less rate of tooth displacement. These results showed that IL-1Ra has an anti-inflammatory role that leads to a downregulation of the orthodontic tooth movement.
The production of IL-1β is inducted from the processing and the activation of a pro-IL-1β by a protease, the caspase-1. Indeed, an apoptosis process occurs in conjunction with the inflammatory one that eliminates the hyalinized periodontal tissue formed during the early stages of orthodontic movement. Caspase-1 is the most important mediator of inflammation and apoptosis responses, activated by inflammatory signals as alterations in the intracellular ionic milieu. In a rat model under orthodontic treatment, caspase-1 expression is increased, and the level of caspase-1 changes with different temporal phases of orthodontic tooth movement . If the local orthodontic application of force is excessive, or else if in the body there is an hyper-expression of caspase-1 by a kind of diseases like rheumatoid arthritis, an irreversible root resorption and a deformation of periodontal tissues might appear. Researchers propose that, because of the primary role of caspase-1 in inflammatory response due to orthodontic tooth movement, a method to preserve the structure of periodontal ligament may be the administration of the inhibitors of caspase-1 activity such as VX-765  and Pralnacasan .
1.2. VEGF Localization during Orthodontic Tooth Movement in Animal Models
Vascular endothelial growth factor is the primary mediator of angiogenesis and it increases vascular permeability. This cytokine is involved in tissue neoformation that is strictly correlated with the presence of blood vessels. During orthodontic tooth movement, compressive forces induce angiogenesis of periodontal ligament together with the role of mediator of the VEGF. The localization of VEGF was analyzed in vivo in rat periodontal tissues during experimental tooth movement. In this analysis, 15 male Wistar rats were used. A compressive force at 150 mN was applied by means of a uniform standardized compressive spring placed between the right and left upper first molars in each rat’s mouths. The maxillary bone was removed by the animals and it was analyzed with immunohistochemical staining. In the experimental animals, VEGF immunoreactivity was in vascular endothelial cells, osteoblasts, osteoclasts in resorption lacunae, in fibroblasts adjacent to hyalinized tissue, a local necrotic area in compressed zone, and in mononuclear cells in periodontal tissues from the animals . VEGF mRNA was also detected in fibroblasts and osteoblasts in tension area of mice periodontal ligament during experimental tooth orthodontic movement . The protocol included 10 mice, divided between experimental and control animals, and provided the analysis of premaxillary bone frontal sections . Therefore, VEGF exerts a fundamental role in remodeling periodontal ligament and is also involved in bone resorption and formation.
1.3. Relation among Some Markers of Bone Cell Proliferation and M-CSF with Orthodontic Movement
There are other studies that examine a variety of proliferation markers expressed during orthodontic tooth movement. For instance, the high presence of the antigen KI-67, nuclear protein associated with cellular proliferation and ribosomal RNA transcription, and of RANKL, a key factor for osteoclast differentiation and activation [19, 20], indicates the recruitment of osteoclasts in compression areas , whereas, the expression of Runx2, a transcription factor associated with osteoblast differentiation, shows the increase of differentiated osteoblasts in tension areas . In other studies, researchers analyzed the collagen type 1 (3.6Col1) and the bone sialoprotein (BSP) in periodontal ligament, using transgenic mice containing transgenes of these promoters fused with green fluorescent proteins (GFP), and they discovered that 3.6Col1-GFP and BSP-GFP cells have an increase on the tension side of the periodontal ligament [22, 23].
Another important role in tooth movement is played by the macrophage colony-stimulating factor (M-CSF), an early osteoclast differentiation factor, that increases the rate of osteoclastic recruitment and differentiation .
In particular, optimal dosages of M-CSF correlated with measurable changes in tooth movement and gene expression, providing potential for clinical studies in accelerating tooth movement.
2. Rats as Models for Orthodontic Movement
Up to now, a large number of studies in various species of animals, such as cats, dogs, and rats, have been done to enlighten the biological response to periodontal ligament. Rats are the most used animals for studying tooth movement, even if there are advantages and disadvantages . Among the disadvantages, it must be remembered that the alveolar bone of rats is more dense than in humans, and there are no osteons. Indeed, the osteoid tissue along the alveolar bone surface in rats is less, their bone extracellular matrix has a few mucopolysaccharides, and, finally, the calcium concentration is more controlled by intestinal absorption. Disparities have been reported also in the arrangement of the peritoneal fibers and in the supporting structures, as in the root formations, which seem to be faster. Notwithstanding these disadvantages, rats are considered a good model to study orthodontic tooth movement. Indeed, they are relatively inexpensive, the histological preparation of their material is easier than other animals, and transgenic strains are almost exclusively developed in small rodents.
Clinical studies show that there are different phases in tooth movement. The application of force during orthodontic tooth movement results in bone resorption by osteoclasts and deposition by osteoblasts on the pressure and tension sides of the periodontal ligament. Recent studies in mice demonstrate that preosteoclasts, and not monocytes, may be recruited to the periodontal ligament during orthodontic tooth movement, and these cells may be targeted for acceleration of tooth movement.
3. Concluding Remarks
Knowledge regarding the biological mechanisms involved in orthodontic tooth movement appears to be of considerable importance for orthodontists that may modulate mechanoresponses and inflammatory process, accelerating or decelerating tooth movement, by adding various exogenous substances, taking also in consideration the condition of health of each orthodontically treated subject.
The authors thank R. De Lucia for her support in the drafting of the paper.
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