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Current Oral Health Reports

, Volume 1, Issue 1, pp 43–49 | Cite as

Whole Tooth Regenerative Therapy Using a Bioengineered Tooth Germ

  • Kei Nakajima
  • Masamitsu Oshima
  • Takashi TsujiEmail author
Stem-cell Biology for Tooth and Periodontal Regeneration (M Bartold, Section Editor)

Abstract

Dental disorders, including dental caries and periodontal disease, can cause fundamental problems for oral functions, such as enunciation, mastication and occlusion, as well as general health issues. Tooth regenerative therapies for tissue repair and whole tooth replacement are currently being developed as novel treatment approaches. As a form of bioengineered organ replacement, whole tooth replacement therapy is considered an important model system for next-generation regenerative therapy. We recently reported bioengineered tooth replacements after transplantation of a bioengineered tooth germ or mature tooth unit comprising the bioengineered tooth and periodontal tissues. Whole tooth regenerative therapy has the potential to fully restore tooth function, including masticatory potential in response to mechanical stress and perceptive potential for noxious stimulation. In this review, we describe recent findings and technologies underpinning tooth regenerative therapy.

Keywords

Organ germ method Bioengineered tooth Bioengineered tooth germ Bioengineered tooth unit Tooth development Epithelial-mesenchymal interaction Cell compartmentalisation Tooth regeneration Tooth physiological function Occlusion Organ replacement regenerative therapy 

Introduction

Functions of teeth such as enunciation, mastication and occlusion are important components of a healthy life [1]. The tooth is of ectodermal origin, its development is regulated by reciprocal epithelial-mesenchymal interactions [2, 3], and it has distinctive hard tissues that include enamel, dentin, and cementum. Teeth also contain a soft connective tissue such as pulp and are surrounded by another soft connective tissue, periodontal ligament. Both of these tissues contain nerve fibres and blood vessels to maintain tooth homeostasis [4]. Dental disorders, including dental caries, periodontal disease or trauma, cause fundamental problems for oral function and are associated with oral and general health issues [1]. Conventionally, tooth restoration involves replacement with artificial materials including dentures or dental implants [5, 6]. Although these artificial therapies are widely applied to the rehabilitation for tooth loss, there have been recent improvements that enhance the biological functions underlying tooth movement through bone remodelling [7].

Current advances in future regenerative therapies have been influenced by many previous studies of embryonic development, stem cell biology and tissue engineering technologies [8, 9]. To restore partial loss of organ function and to repair damaged tissues, attractive regenerative therapy concepts include stem cell transplantation [10] and cytokine therapy targeted to structural and functional diseases [11]. Tooth-derived stem cells and the cytokine networks that regulate tooth development have been well characterised at the molecular level [7, 12]. Dental pulp stem cells (DPSCs) and stem cells from human exfoliated deciduous teeth (SHED) have been isolated from the dental pulp of human permanent third molars and exfoliated deciduous teeth, respectively [13, 14]. DPSCs and SHED are thought to be tooth tissue-derived stem cells with high proliferative capacities and sufficient potency to develop into odontoblasts, adipocytes and neural-like cells. Apical papilla contain unique stem cells, known as stem cells from apical papilla (SCAP), that have a high proliferative potential, which is reflected by high levels of telomerase activity and multi-potent differentiation capability that produces odontoblasts and adipocytes [15]. Furthermore, periodontal ligament-derived stem cells (PDLSCs), which have also been identified in adult human periodontal ligaments, can be cultured as stem cells in vitro, and can differentiate into all periodontal cell types after transplantation in vivo [16]. These advances can be applied to the repair of the dentin-pulp complex and periodontal tissues, including the alveolar bone, by replacing enriched and purified stem cells [17, 18, 19].

The ultimate goal of regenerative therapy is to develop fully functional bioengineered tissues that can replace lost or damaged organs following disease, injury or aging [9, 20]. In the dental field, tooth regenerative therapy involves the replacement of a lost or damaged tooth with a bioengineered tooth reconstructed from stem cells and with the potential to generate a functional tooth unit, including the whole tooth and periodontal tissue surrounding the alveolar bone [19]. The establishment of tooth replacement regenerative therapy is anticipated in the near future as a novel and successful biological treatment that will provide essential functional recovery of lost teeth to satisfy aesthetic and physiological requirements [21]. Many approaches to replace missing teeth have been evaluated over the past three decades, including three-dimensionally bioengineered teeth and tooth germ generation using biodegradable materials and cell aggregation methods [19, 20, 22]. The first reports of fully functioning bioengineered tooth replacement with correct tissue structure, masticatory ability, responsiveness to mechanical stress and perceptive potential following transplantation into tooth loss region were recently published [23, 24•, 25••, 26•]. In this review, we describe the most recent findings and technologies for whole tooth replacement, which have the potential to provide functional recovery and entirely replace the artificial materials currently used in dental replacements.

Tooth Development

Organs such as hair, glands, kidneys and teeth arise from their respective germs, which are induced by reciprocal interactions between epithelial and mesenchymal tissues in the developing embryo [2, 17]. The mechanisms of tooth organogenesis are also regulated by reciprocal epithelial and mesenchymal interactions, particularly those involved in stem cell, signalling molecule and transcription factor pathways. In tooth germ development, the dental lamina first thickens (lamina stage), followed by epithelial thickening (placode stage) at the sites of future teeth and subsequent epithelial budding to the neural crest-derived ecto-mesenchyme. Tooth germ formation is initiated at embryonic days (ED) 10-11 in mice by epithelial signals, e.g., FGF8, BMP4, Shh, TNF and Wnt10b. These signals induce the expression of transcription factors, e.g., Barx1, Dlx1/2, Lhx6, Lhx7 Msx1, Pax9 and Gli, in the dental mesenchyme, which then condense around the developing epithelial bud (bud stage) [2, 3, 17]. At ED14 (cap stage), a first enamel knot known as the transient epithelial signalling centre, which expresses several signalling molecules including Shh, BMPs, FGFs and Wnts, is thought to regulate the epithelial-mesenchymal interactions. The terminal differentiation of dental epithelial and dental mesenchymal cells into ameloblasts and odontoblasts, respectively, occurs at ED16-18 (bell stage). These progenitor cells secrete a collagenous extracellular matrix that mineralises into the enamel and dentin matrix at the epithelium–mesenchyme interface. Tooth morphogenesis, including tooth size and shape, are thought to be regulated by signalling molecules such as the BMPs and FGF4 emanating from the secondary enamel knots, which regulate the cusp pattern of the mature natural tooth in the early bell stage to form the tooth crown [17, 27]. The outer mesenchymal cells of tooth germ form the dental follicle, which can generate periodontal tissue, including cementum, periodontal ligament and alveolar bone. After tooth crown formation, tooth root formation is initiated, followed by tooth eruption in the oral cavity.

Technological Developments for Whole Tooth Regeneration

The current approach to generating ectodermal organs such as teeth, hair follicles and salivary glands is to recreate organogenesis by mimicking the epithelial-mesenchymal interactions that occur in the developing embryo, thereby developing fully functional bioengineered organs from bioengineered organ germ generated from immature stem cells via three-dimensional cell manipulation in vitro [20, 21, 28, 29, 30]. For tooth regeneration, a concept has been proposed in which a bioengineered tooth germ is transplanted into the recipient jawbone and subsequently develops into a functional mature tooth (Fig. 1A, upper panel) [25••]. Transplantation of a bioengineered mature organ would enable full function immediately in vivo [3, 8, 26•]. Thus, it is also anticipated that it will be possible to transplant a bioengineered tooth unit including a mature tooth, periodontal ligament and alveolar bone to achieve engraftment through physiological bone integration with the recipient’s alveolar bone (Fig. 1A, lower panel) [26•]. To achieve whole tooth replacement, the first major issue is to develop a three-dimensional cell manipulation technology using completely dissociated epithelial and mesenchymal cells in vitro. Two conventional approaches and a novel cell manipulation method are currently being examined for the purpose of generating bioengineered tooth germ or mature tooth and are described below.
Figure 1

(A) Strategies for the whole tooth replacement regenerative therapies. Functioning teeth can be regenerated in vivo by transplanting bioengineered tooth germ reconstituted from epithelial and mesenchymal cells via the organ germ method or by transplanting bioengineered tooth units with periodontal ligament and alveolar bone developed from bioengineered tooth germ. E: epithelium, M: mesenchyme. (B) Coordination with the oral and maxillofacial regions. Functional teeth should achieve sufficient masticatory performance with occlusion to the opposing teeth. Tooth function is also responsive to mechanical stress and noxious stimulations, in which it cooperates with both the oral and maxillofacial regions. Noxious stimulations such as mechanical stress and pain, which are detected by the sensory nerves in the pulp and by the periodontal ligament of the tooth, are transduced by the corresponding perceptions of the central nervous system via the trigeminal spinal nucleus in the medullary dorsal horn

  1. 1)

    Bioengineering of tooth germ using a biodegradable scaffold

     
Three-dimensional tissue engineering methods have provided the scaffold technology needed to regenerate suitably shaped tissues by seeding potential cells onto degradable materials fabricated from either natural ingredients or synthetic polymers. This technique has shown high utility in three-dimensional tissue engineering methods, and these preparations have been used in clinical applications such as bone and cartilage regenerative therapies [9, 31, 32]. Studies using polyglycolic acid and poly-L-lactate-co-glycolide copolymer (PLA/PLGA) [33, 34, 35] or collagen/gelatine sponge as scaffolding materials have reported that seeding epithelial and mesenchymal cells isolated from murine or porcine tooth bud onto a tooth-shaped scaffold could generate small tooth structures, including pulp, dentin and enamel, but not periodontal tissue [19, 21, 35, 36, 37, 38, 39]. Although the scaffold method would be practical for tooth shape and size control, it has critical limitations, including tooth formation frequency and the appropriate replication of tooth tissue structures such as the enamel–dentin complex formation that underlies proper arrangements of ameloblast and odontoblast cell lineages, which are achieved through epithelial-mesenchymal interactions as well as natural tooth development [4, 21].
  1. 2)

    Reconstruction of tooth germ using cell aggregation methods

     
Cell aggregation is a typical bioengineering protocol that aims to reconstitute a bioengineered organ germ that properly reproduces epithelial-mesenchymal interactions and organogenesis [21, 38]. Transplantation of bioengineered cell aggregates using hair follicles and mammary gland-derived stem cells has shown promise for regenerating correct organ structures with proper arrangements of different cell types in vivo [30, 40]. Tooth germs constructed from precipitates of dental epithelial and mesenchymal cells by using cellular centrifugation can result in complete tooth formation [41, 42]. Mixed cell aggregates of dissociated epithelial and mesenchymal cells isolated from molar tooth germ can also develop into a tooth with the correct structure, following epithelial cell sorting and subsequent epithelial and mesenchymal cell self-reorganisation [43]. Although this technique reconstructs organogenesis, the frequency of tooth development and tissue formation is insufficient.
  1. 3)

    Novel three-dimensional cell manipulation methods for bioengineered tooth germ: the “Organ Germ Method”

     

To achieve precise replication of the processes associated with organogenesis, an in vitro three-dimensional novel cell manipulation method designated as a bioengineered organ germ method has been developed [23, 24•]. This method involves cell compartmentalisation of epithelial and mesenchymal cells from mouse embryonic cap-stage tooth germs at high cell density in a type I collagen gel to mimic multicellular assembly and epithelial-mesenchymal interactions as well as natural tooth development. The bioengineered tooth germ generates a structurally correct tooth after transplantation in an organ culture in vitro, as well as following placement into a subrenal capsule in vivo [23]. Tooth morphology is defined by the macromorphological features of crown size and tooth length, and the micromorphological features of the number and position of the cusps. The crown size is based on the reaction-diffusion model, and the regulation of the cusp number and position is thought to be closely involved in the formation of the secondary enamel knot [17]. Bioengineered tooth germs were reconstructed using various contact lengths between the epithelial and mesenchymal cell layers, and thereby the crown widths and cusp numbers of these bioengineered teeth were dependent on the contact length of the bioengineered tooth germs [44•]. These technologies have the potential to be adapted for successful functional tooth replacement in vivo, and are expected to represent an innovative advance in bioengineered organ replacement regenerative therapies.

Functional Tooth Replacement Regenerative Therapy

Teeth have important oral functions such as mastication, pronunciation, and facial aesthetics, which have an important influence on quality of life [1]. These tooth-related functions are achieved along with masticatory muscles and the temporomandibular joint under the control of the central nervous system (Fig. 1B) [45]. For successful tooth replacement regenerative therapy, a tooth developed from a bioengineered germ or a transplanted bioengineered mature tooth unit must be capable of being successfully grafted into the lost tooth region in an adult oral environment and achieve full functionality, including sufficient masticatory performance, biological cooperation with the periodontal tissues and afferent responsiveness to noxious stimulations in the maxillofacial region [1].
  1. 1)

    Transplantation of bioengineered tooth germ or a bioengineered mature tooth unit as a tooth replacement therapy

     

Successful tooth regenerative therapy, via transplantation of a bioengineered tooth germ into the lost tooth region, requires that the transplanted germ erupt and occlude properly with the opposing tooth in the adult jawbone. Tooth eruption is a cooperative regulatory mechanism that involves the tooth germ cell component and surrounding alveolar/jawbone [46]. Dental follicle cells migrate from near the surface of the enamel organs and dental papillae to form the cementum, periodontal ligament, and alveolar bone. These cells contribute to overlying bone resorption by enzymatic degeneration during growth and the axial movement of the teeth during the process of tooth eruption [47]. Bioengineered tooth germs can develop the correct structure in a tooth cavity, and normal tooth germs can develop and also erupt in a toothless diastema region [48]. Furthermore, in animal models, bioengineered tooth germs can form the correct tooth structure in the oral cavity [23] and can successfully erupt 37 days after transplantation. The bioengineered tooth subsequently reaches the occlusal plane and maintains occlusion with the opposing tooth from 49 days onwards [25••].

To produce a transplanted bioengineered tooth unit comprising a mature tooth, periodontal ligament and alveolar bone, the most critical consideration is whether the unit can be grafted into the tooth loss region with subsequent bone integration, which involves bone resorption of the alveolar bone of the bioengineered tooth unit through natural bone remodelling at the recipient site. Bioengineered teeth have been successfully grafted at 40 days and subsequently maintained with a functional periodontal ligament originating from the bioengineered tooth unit and traversing to the adjacent bone, implying successful bone integration [26•]. Furthermore, the enamel and dentin hardness of the bioengineered tooth components were in the normal range when analysed by the Knoop hardness test [25••, 26•]. These approaches demonstrate the potential to restore masticatory performance and natural tooth tissue through new technologies.
  1. 2)

    The biological response of a bioengineered tooth to mechanical stress

     
Tooth loss and functional disorders in periodontal ligaments cause fundamental problems for oral functions by affecting pronunciation, mastication, occlusion, and associated health issues [1]. The periodontal ligament plays an essential role in the pathogenic and physiological responses of teeth to extreme mechanical forces from bone remodelling accompanied by orthodontic tooth movement (Fig. 1B) [47]. Autologous tooth transplantation following a traumatic dental injury has demonstrated that teeth with healthy periodontal ligament cells can prevent ankylosis and attach successfully to the surrounding alveolar bone tissue [49]. By contrast, the absence of a periodontal ligament in osseo-integrated dental implants is associated with deficiencies of the essential tooth functions and in the natural structural relationship with the root and alveolar bone [7, 50]. Biological regenerative therapy using functional periodontal tissue has been shown to be effective in restoring normal tooth functions as an alternative to artificial therapy [51]. The periodontal ligaments of bioengineered teeth that erupted following transplantation of a bioengineered tooth germ resulted in the formation of mature tooth units with functional tooth movement equivalent to that of natural teeth. Bone remodelling was successfully reproduced via the proper localisation of osteoclasts and osteoblasts in response to mechanical stress. These findings indicate that a bioengineered tooth can replicate critical dental functions and subsequently lead to the restoration and re-establishment of functional teeth within the maxillofacial region [25••, 26•].
  1. 3)

    Proprioception potential of neuronal response in bioengineered teeth

     

Teeth are a peripheral target organ for the sensory trigeminal and sympathetic nerves, both of which play important roles in homeostasis and protection [50]. The perceptive potential for noxious stimulation, including mechanical stress and pain, are important for proper tooth function. Trigeminal ganglional neurons, which innervate the pulp and PDL, can respond to these stimulations and transduce the perceptions to the central nervous system (Fig. 1B). It is anticipated that tooth regenerative therapies will be able to recover the neuronal perceptive ability of mechanical forces, which are lacking in implant patients [52]. Recently, nerve fibres, such as the sensory and sympathetic nerves, have been shown to innervate both the pulp and PDL of a regenerated tooth that had successfully erupted following the transplantation of not only bioengineered tooth germ, but also a bioengineered tooth unit [25••, 26•]. These bioengineered teeth have the appropriate perceptive potential for noxious stimulations, such as pulp injury and orthodontic force, and can also properly transduce these stimulations to the central nervous system through c-Fos immunoreactive neurons [25••, 26•]. These findings indicate that bioengineered teeth can indeed restore the proprioceptive potential to identify and respond to noxious stimulation within the maxillofacial region.

Future Perspectives for Tooth Regeneration

There are several problems that must be solved before bioengineered teeth become feasible. To fully realise the practical clinical application of tooth regeneration, suitable cell sources must be identified. Ideally, tooth regenerative therapy should employ the patient’s own cells to avoid immunological rejection [20]. Recent studies of stem cell biology and embryonic development have led to considerable advances in the potential of cell sources for tissue repair and organ regeneration, including tooth regenerative therapy [10, 18]. Tooth tissue-derived stem cells such as DPSCs, SHED, SCAP and PDLSCs [13, 14, 15, 16, 53] can differentiate into dental cell lineages and contribute to the turnover and supply of various cell populations. These lineages will be useful cell sources for stem cell transplantation therapy for dental tissue repair [12, 20], but there is no evidence that these stem cells have the potential to form whole teeth.

Current whole tooth regenerative therapy research is attempting to induce bioengineered tooth germ to develop a fully functioning tooth using embryonic tooth germ-derived epithelial and mesenchymal cells via the organ germ method [23, 24•, 25••, 26•]. In the future, cell sources that have the tooth-forming ability to reproduce the epithelial and mesenchymal interactions for tooth organogenesis will need to be identified from the various tissue-derived stem cell populations isolated from patients. Other candidate cell sources for whole tooth regeneration include embryonic stem (ES) cells and induced pluripotent stem (iPS) cells, which are capable of differentiating into endoderm, ectoderm and mesoderm [54]. iPS cells have recently been generated from various oral tissues [55, 56, 57], but their application will require the establishment of reprogramming procedures for dental epithelium and mesenchyme fates. Although there are multiple candidates for tooth developmental genes that promote significant expression of dental epithelial and mesenchymal cells, the master genes responsible for tooth development remain to be discovered. An important issue for identifying a future tooth regenerative cell source is the identification of specific combinations of factors capable of reprogramming non-dental cells to dental epithelium and mesenchyme.

Tooth types such as incisors, canines, premolars and molars have unique morphological features that are programmed at predetermined sites in the oral cavity during tooth development. Several studies have proposed molecular mechanisms for tooth morphology regulation [30, 44•, 58]. Tooth size, crown and root shape are important considerations when generating a bioengineered regenerated tooth with proper functional occlusion and aesthetics.

Conclusions

The progress of regenerative technology is remarkable, and many patients and clinicians are anticipating the implementation of whole tooth regenerative therapy. Further studies are required to establish bioengineering technologies that can control tooth morphology, including tissue engineering using scaffolds, and the identification of morphogenesis-related genes and appropriate cytokines. Tooth regenerative therapy is now regarded as a crucial study model for future replacement regenerative therapies that can be applied to more complex organs, and will contribute substantially to the knowledge and technology required to regenerate organs [20, 21].

Notes

Compliance with Ethics Guidelines

Conflict of Interest

Dr. Kei Nakajima, Dr. Masamitsu Oshima, and Dr. Takashi Tsuji each declare that there are no potential conflicts of interest relevant to this article.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

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Copyright information

© Springer International Publishing AG 2013

Authors and Affiliations

  • Kei Nakajima
    • 1
    • 2
  • Masamitsu Oshima
    • 3
  • Takashi Tsuji
    • 1
    • 3
    • 4
    Email author
  1. 1.Department of Biological Science and Technology, Graduate School of Industrial Science and TechnologyTokyo University of ScienceNodaJapan
  2. 2.Department of Clinical PathophysiologyTokyo Dental CollegeChiba-shiJapan
  3. 3.Research Institute for Science and TechnologyTokyo University of ScienceNodaJapan
  4. 4.Organ Technologies Inc.TokyoJapan

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