|Year : 2015 | Volume
| Issue : 1 | Page : 13-18
|Reforming craniofacial orthodontics via stem cells
Pritam Mohanty1, N.K.K. Prasad2, Nivedita Sahoo1, Gunjan Kumar3, Debapreeti Mohanty4, Sushila Sah1
1 Department of Orthodontics and Dentofacial Orthopedics, Kalinga Institute of Dental Sciences, KIIT University, Bhubaneswar, Odisha, India
2 Department of Orthodontics and Dentofacial Orthopedics, Sri Ramachandra University, Chennai, Tamil Nadu, India
3 Department of Public Health Dentistry, Kalinga Institute of Dental Sciences, KIIT University, Bhubaneswar, Odisha, India
4 Department of Conservative Dentistry and Endodontics, Kalinga Institute of Dental Sciences, KIIT University, Bhubaneswar, India
|Date of Web Publication||23-Feb-2015|
N4/262, IRC Village, Nayapalli, Bhubaneswar - 751 015, Odisha
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Stem cells are the most interesting cells in cell biology. They have the potential to evolve as one of the most powerful technologies in the future. The future refers to an age where it will be used extensively in various fields of medical and dental sciences. Researchers have discovered a number of sources from which stem cells can be derived. Craniofacial problems are very common and occur at all ages. Stem cells can be used therapeutically in almost every field of health science. In fact, many procedures will be reformed after stem cells come into play. This article is an insight into the review of the current researches being carried out on stem cells and its use in the field of orthodontics, which is a specialized branch of dentistry. Although the future is uncertain, there is a great possibility that stem cells will be used extensively in almost all major procedures of orthodontics.
Keywords: Orthodontics, periodontium, root resorption, stem cells, Temporomandibular joint defects
|How to cite this article:|
Mohanty P, Prasad N, Sahoo N, Kumar G, Mohanty D, Sah S. Reforming craniofacial orthodontics via stem cells. J Int Soc Prevent Communit Dent 2015;5:13-8
|How to cite this URL:|
Mohanty P, Prasad N, Sahoo N, Kumar G, Mohanty D, Sah S. Reforming craniofacial orthodontics via stem cells. J Int Soc Prevent Communit Dent [serial online] 2015 [cited 2022 Jan 25];5:13-8. Available from: https://www.jispcd.org/text.asp?2015/5/1/13/151966
| Introduction|| |
Nowadays faster orthodontic treatment is one of the major demands of the patient population, which is not adequately met by the orthodontists. Low friction and self-ligating bracket systems, robot preformed arch wires, rapid canine retraction, and alveolar corticotomies are some examples of the approaches that aim to reduce the time required by orthodontic therapy.  These procedures have definitely brought better results, but they are not the ultimate solution to all our problems - newer and better technologies are always welcome. Technologies such as stem cell therapy hold a great potential and can bring a revolutionary change in the field of health science. The knowledge of stem cells and its implications will help the orthodontists to modify their treatment planning, which will be acknowledged by the patient. This article will review the literature on the potential clinical use of stem cells in craniofacial deformities, with reference to the orthodontic field.
| Stem Cells|| |
It was E.D. Wilson who in his classic textbook, "The Cell in Development and Inheritance," first coined the phrase 'stem cell,' in 1896.  Stem cells are 'undifferentiated cells that can proliferate and have the capacity for self-renewal and the ability to produce one or more highly differentiated progenitors'. , However, this definition is not fully accepted after the introduction of concepts like de-differentiation and transdifferentiation. In 2007, Dr. James Thomson, in the United States, and Dr. Yamanaka, in Japan, simultaneously discovered that adult human cells could be reprogrammed back to an embryonic state by overexpressing the powerful stem cell genes. These new type of stem cells are called induced pluripotent stem cells (IPSC). ,
Essentially, stem cells are of two types: Embryonic stem cells and Adult stem cells. The embryonic cells are pluripotent and can differentiate to all cell lineages in vivo.  Human embryonic stem cells are derived from the inner cell mass of a blastocyst that has been fertilized in vitro. , They are virtually immortal due to their high expression of telomerase, the enzyme complex responsible for maintaining telomere lengths and chromosomal stability during cellular division.  However, their growth is difficult to control and they are fairly sensitive. ,
An adult stem cell can be defined as a cell residing within an adult tissue that divides, either autonomously or in response to regulated signals, to produce cells that contribute to organismal homeostasis.  Adult stem cells or extra-embryonic stem cells are partly specialized cells, as they are not capable of forming all types of cells. The list of adult tissues containing stem cell repositories are growing and include the bone marrow, peripheral blood, brain, spinal cord, dental pulp, blood vessels, skeletal muscle, epithelia of the skin and digestive system, cornea, retina, liver, and pancreas.  Unfortunately, the isolation of adult stem cells with sufficient purity and quantity is still complicated. 
| The Need of Stem Cells|| |
Worldwide there is a significant percentage of the population suffering from oral and craniofacial defects, which demand oral and craniofacial tissue engineering. Techniques like autografts, allografts, and biomaterial are used to repair these defects. Taking these into consideration, each of them has some limitations. Although autografts are considered as the 'gold standard' for bone regeneration procedures, yet the failure rate is as high as 30%.  The allograft has a great potential for rejection and infection transfer. Freeze-drying, demineralization, and irradiation to reduce graft immunogenicity can also reduce the structural integrity; leading to a graft fracture. ,, Bone allografts are not osteogenic and there is slower integration in the host bed.  Besides this, grafting procedures include risks such as donor site morbidity, unpredictable resorption, limited quantities available, and the need to include additional surgical sites.  Alloplasts have only an osteoconductive property and lack osteoinductive and osteogenic properties,  therefore, bone formation is uncertain in this case. Biomaterials, such as implants, and bone substitutes such as bovine and the like, for long-term complications, include, stress shielding, loosening, and mechanical or chemical breakdown of the material itself.  Thus, there is a demand for a method or material that is less invasive, reduces the risk of morbidity, has the ability to adapt itself along with the tissue, and can be in a harmonious relationship with the adjacent hard and soft tissues.
Stem cells have three specific properties: 
- They are unspecialized cells that renew themselves for long periods through cell division
- Under certain conditions stem cells can be induced to become cells with special functions, with the capability of self-renewal
- Stem cells give rise to specialized cells.
Thus, their properties of differentiating into any kind of cells and self-renewal can pave new pathways for treatment.
| The Promise of Stem Cells to Orthodontists|| |
With the recent advances in the understanding of stem cell biology, certain opportunities can be provided to the orthodontist such as:
Shorter treatment time
In a study,  embryonic stem cells have been differentiated into cartilage cells and implanted on artificially created cranial osseous defects. In comparison to the control group, the group that received the implanted tissue had a significantly faster response. It is known that for any damaged tissue to recover there should be regeneration of blood vessels in that region. Mesenchymal stem cells (MSCs) express and secrete stromal cell-derived factor 1 (SDF-1), the vascular endothelial growth factor (VEGF); the basic fibroblast growth factor (bFGF); matrix metalloproteinases (MMPs), and other cytokines that are important for angiogenesis.  Thus, stem cells can provide a sufficient substrate for neoangiogenesis. In a study, primary marrow-derived, cultured mesenchymal cells that were introduced into ceramic showed a strong osteogenic potential, with bone forming in the pore regions of the ceramic as early as two weeks after in vivo implantation.  Stem cells also secrete bioactive factors that suppress the local immune system, inhibit fibrosis and apoptosis, enhance angiogenesis, and stimulate mitosis and differentiation of the tissue intrinsic reparative process.  From these studies it is clear that stem cells can enhance the treatment by increasing the rate of healing and regeneration, thereby, reducing the treatment time.
Periodontal health consideration
The periodontium is the only supporting system of the tooth. Nowadays, many people suffer from periodontal disease. Periodontal complications are one of the most common side effects linked to orthodontics; they occur in various forms, from gingivitis to periodontitis, dehiscence, fenestrations, interdental fold, gingival recession or overgrowth, and black triangles.  One such example - band impingement - may directly compromise the local resistance related to subgingival pathogens in susceptible patients and result in damage to both interproximal gingival tissues and alveolar crestal bone.  This is the reason why it becomes very essential for an orthodontist to maintain the ortho-perio relationship while carrying out any orthodontic procedures. Surprisingly, periodontal ligament stem cells (PDSCs) are capable of regenerating the wounded periodontium in rats; surpassing the repair capacity of embryonic cells.  Thus, stem cells can be used to regenerate and repair periodontal tissues.
In a study,  human periodontal cell sheets were transplanted into a mesial dehiscence model, in athymic rats, where the periodontal ligament-like tissues - which included an acellular cementum-like layer and fibrils anchoring into this layer - were identified at their site of placement. Such regeneration was not observed in the nontransplanted controls. Another in vivo study was conducted using human adult PDSCs and transplanted into an athymic rat model, and the data showed that human adult PDSCs were capable of regenerating elements of bone and collagen fibers.  However, complete regeneration of the periodontal complex was a big challenge to overcome, especially in a diseased state with inflammatory factors, including cytokines.  Human PDLSCs were transplanted into surgically created defects in the periodontal area of the mandibular molars in immunocompromised rats. They were integrated into the PDL tissue, which resulted in them homing to the surfaces of the alveolar bone and tooth root.  When the PDLSCs were treated with dentin noncollagenous proteins, they showed an increased proliferation and adhesion ability.  Dental pulp stem cells (DPSCs) have the highest osteogenic potential among bone marrow mesenchymal stem cells (BMMSCs) and periosteal cells, indicating a useful cell source for tissue engineered bone around the dental implants.  These look promising, but there is still a long way to go before they enter the clinics.
Lesser root resorption
External apical root resorption is the most common  and undesirable sequela of orthodontic treatment.  In most studies of root resorption, treatment factors top the list of the 'usual suspects'.  They are probably caused on account of the removal of the necrotic tissue from areas of the periodontal ligament that have been compressed by an orthodontic load.  However, root resorption is multifactorial, with a complex etiology, but the condition appears to result from a combination of individual biological variability, genetic predisposition, and the effect of a mechanical factor. ,, According to recent studies, odontoblasts can be derived from mesenchymal stem cells (MSC), stem cells from an exfoliated deciduous tooth (SHED), dental pulp stem cells (DPSC), and apical papilla stem cells (SCAP), while cementoblasts can be derived from mesenchymal stem cells (MSC) and dental follicular stem cells (DFSC).  Thus, these kinds of stem cells may be used prior to the treatment, to prevent root resorption or post treatment to repair the damage.
Using stem cell therapy instead of bone graft surgery will relieve the patient from the extra major surgical procedures and the pain of iliac crest bone grafts. It is a minimally invasive technique.  Other advantages include, less failure cases as the body's own cells are used and there is of course natural regeneration. Stem cells can also accelerate the healing process, as has been done in a study by Wu et al. It has been found that bone marrow mesenchymal stem cell (BM-MSC)-treated wounds exhibit significantly accelerated wound closure, with increased re-epithelialization, cellularity, and angiogenesis.
| Orthodontic Implications of Stem Cell Therapy|| |
Repair of the alveolar bone
Unwanted alveolar bony defects are often created after orthodontic extractions and repair of these defects is needed to avoid the risk of dehiscence and other periodontal insults at a later stage, after the teeth have been retracted into the extraction site.  Resorption of an edentulous or partially edentulous alveolar ridge or bone loss on account of periodontitis or trauma will require alveolar bone augmentation prior to placement of the implant.  Stem cells can be a potential treatment for rehabilitation of these types of defects. For example, in an experiment conducted on animal models (rats) with traumatic alveolar bone defects on the maxilla, bilaterally, it was found that a composition of bone marrow stem cells (BMSCs) and fibrin glue (FG) had been suggested as a promising method to repair the alveolar bone defect. 
In a recent study,  the tissue repair cells were grafted into the osseous defects of the jaw of 12 patients and the biopsies were harvested for analysis at six and twelve weeks. Reconstruction was completed with an oral implant therapy and was observed for 12 months postoperatively. It was demonstrated clinically, radiographically, and histologically that the cell therapy accelerated the regenerative response. There was also significant reduction in the need for secondary bone grafting procedures in this group.
The alveolar cleft is a highly prevalent congenital malformation, where 75% of the patients with cleft lip and palate display osseous defects of the premaxilla alveolar bone.  Contemporary treatments of patients with alveolar cleft defects involve autologous bone grafting at the defect site.  These patients often require a secondary bone graft procedure, to allow for eruption of the anterior teeth and orthodontic treatment.  However, in 10-36% of the cases there is graft resorption and later on surgical procedures are needed. , Late complications such as chronic pain, unesthetic scarring at the harvest site, and gait disturbance have often been associated. , Thus, there is a need for an alternative to combat these complications so that the orthodontic treatment of these patients becomes facile and at the same time effectual. In an alveolar cleft osteoplasty of a nine-year-old female patient, mesenchymal stem cells were used instead of bone grafts. After six months the cleft bridged with 79.1% of the grafted region and after nine months the canine and lateral incisor in the affected side erupted in the reconstructed alveolar ridge. 
| Distraction Osteogenesis|| |
Distraction osteogenesis is a surgical approach by which the development of new bone growth in an area subjected to gradual tension and stress occurs by deliberate separation of the fragments by traction.  Ischemia is a limiting factor during distraction osteogenesis, which can be overcome by using stem cells.  It has even been suggested that using stem cells in distraction osteogenesis may prove to be a potential method to accelerate bone regeneration in the distraction gap and enhance consolidation. 
In a study,  54 New Zealand white rabbits underwent osteodistraction of the left mandible and were randomly divided into group A, group B, and group C (n = 18 in each group). At the end of the distraction, bone marrow mesenchymal stem cells (BMMSCs) transfected with osterix (OSX), autologous BMMSCs, and physiological saline were injected into the distraction gap in groups A, B, and C, respectively. It was observed that there was excellent bone callus formation in groups A and B. The group C animals showed poor bone formation in the distracted callus, when compared to groups A and B.
| Regeneration and Repair of Temporomandibular Joint Defects|| |
Temporomandibular joint disorders (TMD) manifest as pain, myalgia, headaches, and structural destruction, collectively known as degenerative joint disease.  The primary methods used to reconstruct the temporomandibular joint (TMJ) include autogenous bone grafting, such as, harvesting from the rib or the use of alloplastic materials, with neither being ideally suited for the task and sometimes leading to unwanted adverse effects.  The recent advances in stem cell technology assure the construction of a bioengineered TMJ replacement, which is biocompatible and capable of withstanding the physiological loads required for this joint.  Cells from various sources, including articular cartilage cells, fibroblasts, human umbilical cord matrix cells, and mesenchymal stem cells, have been used in efforts to reconstruct the TMJ. , In many studies, a tissue-engineered mandibular condyle was constructed, with stratified layers of cartilage and bone from a single population of BMMSCs, which was molded into the shape of a human cadaver mandibular condyle, with dimensions of 11 × 7 × 9 mm (length × width × height). ,,,
| The Phase of Transition|| |
Stem cells are still controversial and of course their use is uneconomical. One requires high skill and knowledge to handle and use them. There are also no proper studies done on how many stem cells are required to treat a defect. Variable results are seen, for example, implantation of osteo-induced rabbit adipose-derived stem cells (ASCs) and gelfoam scaffolds into rabbit calvarian defects have not significantly improved bony healing when compared with the controls.  In contrast to this, a study has reported improved calvarial defect healing upon implantation of poly lactic-co-glycolic acid scaffolds seeded with human ASCs maintained in vitro, in the presence of osteogenic factors, before implantation.  There are many records of using different kinds of stem cells with different scaffolds, but to date no standard cell-scaffold system exists, which is accepted universally. This is a phase of transition and problems will exist, but they can only be solved by conducting more detailed researches and studies on them.
| Conclusion|| |
Nowadays stem cell therapy is one of the most favored areas of research in craniofacial tissue engineering. However, the fact is that our exposure to this technology remains limited, as it is extremely expensive. Isolation and storage requires a lot of experience, as also high storage and good transport facilities. Stem cell therapy is a multidisciplinary approach. Support from the regulatory bodies, funding agencies, advocacy bodies, ethic bodies, and manufacturing agencies is also needed to make it easily acceptable in our clinical conditions. It will be really fascinating to see craniofacial orthodontists using this therapy on a daily basis to treat patients.
| References|| |
Oliveira DD, Oliveira BF, Soares RV. Alveolar corticotomies in orthodontics: Indications and effects on tooth movement. Dental Press J Orthod 2010;15:144-57.
Svendsen CN, Ebert AD. Encyclopedia of Stem Cell Research. 13 th
ed, Vol. 1 and 2. Thousand Oaks, California: Sage Publications Inc; 2008.
Daruwala N, Mahadevia S, Paneriya PR. Stem cells: The future of dentistry. JADCH 2010;1:12-17.
Polak JM, Bishop AE. Stem cells and tissue engineering: Past, present and future. Ann N Y Acad Sci 2006;1068:352-66.
Takahashi K, Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006;126:663-76.
Jiang Y, Jahagirdar BN, Reinhardt RL, Schwartz RE, Keene CD, Ortiz-Gonzalez XR, et al
. Pluripotency of mesenchymal stem cells derived from adult marrow. Nature 2002;418:41-9.
Strem BM, Hicok KC, Zhu M, Wulur I, Alfonso Z, Schreiber RE, et al
. Multipotential differentiation of adipose tissue-derived stem cells. Keio J Med 2005;54:132-41.
Odorico JS, Kaufman DS, Thomson JA. Multilineage differentiation from human embryonic stem cell lines. Stem Cells 2001;19:193-204.
Wright WE, Piatyszek MA, Rainey WE, Byrd W, Shay JW. Telomerase activity in human germline and embryonic tissues and cells. Dev Genet 1996;18:173-9.
Wu DC, Boyd AS, Wood KJ. Embryonic stem cell transplantation: Potential applicability in cell replacement therapy and regenerative medicine. Front Biosci 2007;12:4525-35.
Xie T, Spradling A. The drosophila ovary: An in vivo
stem cell system. In: Marshak DR, Gardner RL, Gottlieb D, editors. Stem Cell Biology. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 2001. p. 129-48.
Conrad C, Huss R. Adult stem cell lines in regenerative medicine and reconstructive surgery. J Surg Res 2005;124:201-8.
Jackson IT, Helden G, Marx R. Skullbone grafts in maxillofacial and craniofacial surgery. J Oral Maxillofac Surg 1986;44:949-55.
Kumar GP, Hussain SN, Gomes PS, Lopes MA, Fernandes MH, Santos JD. Calcium phosphate ceramics in periodontal regeneration. In Current Trends on Glass and Ceramic Materials. Nandyala SH, Santos JD, editors. UAE/USA: Bentham Science Publishers; 2012. p. 116-41.
Hamer AJ, Strachan JR, Black MM, Ibbotson CJ, Stockley I, Elson RA. Biomechanical properties of cortical allograft bone using a new method of bone strength measurement. J Bone Joint Surg Br 1996;78:363-8.
Gitelis S, Cole BJ. The use of allografts in orthopaedic surgery. Instr Course Lect 2002;51:507-20.
Albert A, Leemrijse T, Druez V, Delloye C, Cornu O. Are bone autografts still necessary in 2006? A three year retrospective study of bone grafting. Acta Orthop Belg 2006;72:734-40.
Jensen SS, Terheyden H. Bone Augmentation Procedures in localized defects in the alveolar ridge: Clinical results with different bone grafts and bone-substitute materials. Int J Oral Maxillofac Implants 2009;24 Suppl :218-36.
Ogunsalu C. Bone substitutes and validation. In: Turkyilmaz I, editor. Implant Dentistry-The Most Promising Discipline of Dentistry. New York, USA: InTech; 2011. p. 129-72.
Yaszemski MJ, Payne RG, Hayes WC, Langer R, Mikos AG. Evolution of bone transplantation: Molecular, cellular and tissue strategies to engineer human bone. Biomaterials 1996;17:175-85.
Kelly EB. Stem Cells. 1 st
ed. Westport, Connecticut, London: Greenwood Publishing Group; 2007. p. 3-6.
Doan L, Kelley C, Luong H, English J, Gomez H, Johnson E, et al
. Engineered cartilage heals skull defects. Am J Orthod Dentofacial Orthop 2010;137:162-3.e1-9.
Semedo P, Burgos-Silva M, Donizetti-Oliveira C, Camara NO. How do mesenchymal stem cells repair? In: Gholamrezanezhad A, editor. Stem Cells in Clinic and Research. Brazil: InTech; 2011. p. 83-104.
Goshima J, Goldberg VM, Caplan AI. The osteogenic potential of culture-expanded rat marrow mesenchymal cells assayed in vivo
in calcium phosphate ceramic blocks. Clin Orthop Relat Res 1991;262:298-311.
Caplan AI, Dennis JE. Mesenchymal stem cells as trophic mediators. J Cell Biochem 2006;98:1076-84.
Preoteasa CT, Ionescu E, Proteasa E. Risks and complications associated with orthodontic treatment. In: Bourzgui F, editor. Orthodontics-Basic Aspects and Clinical Considerations. Rijeka, Crotia: InTech; 2012. p. 403-28.
Vinod K, Reddy YG, Reddy VP, Nandan H, Sharma M. Orthodontic-periodontics interdisciplinary approach. J Indian soc Periodontal 2012;16:11-5.
Nayak BN, Wiltshire WA, Ganss B, Tenenbaum H, McCulloch CA, Lekic C. Healing of periodontal tissues following transplantation of cells in a rat orthodontic tooth movement model. Angle Orthod 2008;78:826-31.
Yamato M, Okano T. Cell sheet engineering. In: Yamato M, Okano T, editors. Materials Today. Vol. 7. UK: Elsevier Ltd.; 2004. p. 42-7.
Grimm WD, Dannan A, Becher S, Gassmann G, Arnold W, Varga G, et al
. The ability of human periodontium-derived stem cells to regenerate periodontal tissues: A preliminary in vivo
investigation. Int J Periodontics Restorative Dent 2011;31:e94-101.
Mudda JA, Bajaj M. Stem cell therapy: A challenge to periodontist. Indian J Dent Res 2011;22:132-9.
Seo BM, Miura M, Gronthos S, Bartold PM, Batouli S, Brahim J, et al
. Investigation of multipotent postnatal stem cells from human periodontal ligament. Lancet 2004;364:149-55.
Ma Z, Li S, Song Y, Tang L, Ma D, Liu B, et al
. The biological effect of dentin noncollagenous proteins (DNCPs) on the human periodontal ligament stem cells (HPDLSCs) in vitro
and in vivo
. Tissue Eng Part A 2008;14:2059-68.
Ito K, Yamada Y, Nakamura S, Ueda M. Osteogenic potential of effective bone engineering using dental pulp stem cells, bone marrow stem cells, and periosteal cells for osseointegration of dental implants. Int J Oral Maxillofac Implants 2011;26:947-54.
Pizzo G, Licata ME, Guiglia R, Giuliana G. Root resorption and orthodontic treatment. Review of the literature. Minerva Stomatol 2007;56:31-44.
McNab S, Battistutta D, Taverne A, Symons AL. External apical root resorption following orthodontic treatment. Angle Orthod 2000;70:227-32.
Sameshima GT, Sinclair PM. Predicting and preventing root resorption: Part II. Treatment factors. Am J Orthod Dentofacial Orthop 2001;119:511-5.
Brudvik P, Rygh P. Root resorption beneath the main hyalinized zone. Eur J Orthod 1994;16:249-63.
Bartley N, Türk T, Colak C, Elekdað-Türk S, Jones A, Petocz P, et al
. Physical properties of root cementum: Part 17. Root resorption after the application of 2.5° and 15° of buccal root torque for 4 weeks: A microcomputed tomography study. Am J Orthod Dentofacial Orthop 2011;139:e353-60.
Weltman B, Vig KW, Fields HW, Shankar S, Kaizar EE. Root resorption associated with orthodontic tooth movement: A systematic review. Am J Orthod Dentofacial Orthop 2010;137:462-76; discussion 12A.
Zahrowski J, Jeske A. Apical root resorption is associated with comprehensive orthodontic treatment but not clearly dependent on prior tooth characteristics or orthodontic techniques. J Am Dent Assoc 2011;142:66-8.
Bluteau G, Luder HU, De Bari C, Mitsiadis TA. Stem cells for tissue engineering. Eur Cells Mater 2008;16:1-9.
Lee KB, Hui JH, Song IC, Ardany L, Lee EH. Injectible mesenchymal stem cell therapy for large cartilage defects--a porcine model. Stem Cells 2007;25:2964-71.
Wu Y, Chen L, Scott PG, Tredget EE. Mesenchymal stem cells enhance wound healing through differentiation and angiogenesis. Stem Cells 2007;25:2648-59.
Wong RK, Hägg EU, Rabie AB, Lau DW. Bone induction in clinical orthodontics: A review. Int J Adult Orthodon Orthognath Surg 2002;17:140-9.
Buser D, Martin W, Belser UC. Optimizing esthetics for implant restorations in anterior maxilla: Anatomic and surgical considerations. Int J Oral Maxillofac Implants 2004;19 Suppl :43-61.
Zhang L, Wang P, Mei S, Li C, Cai C, Ding Y. In vivo
alveolar bone regeneration by bone marrow stem cells/fibrin glue composition. Arch Oral Biol 2012;57:238-44.
Kaigler D, Pagni G, Park CH, Braun TM, Holman LA, Yi E, et al
. Stem cell therapy for craniofacial bone regeneration: A randomized, controlled feasibility trial. Cell Transplant 2013;22:767-77.
Waite PD, Waite DE. Bone grafting for the alveolar cleft defect. Semin Orthod 1996;2:192-6.
Mikoya T, Inoue N, Matsuzawa Y, Totsuku Y, Kajii TS, Hirosawa T. Monocortical mandibular bone grafting for reconstruction of alveolar cleft. Cleft Palate Craniofac J 2010;47:454-68.
Hibi H, Yamada Y, Ueda M, Endo Y. Alveolar cleft osteoplasty using tissue-engineered osteogenic material. Int J Oral Maxillofac surg 2006;35:551-5.
Bayerlein T, Proff P, Heinrich A, Kaduk W, Hosten N, Gedrange T. Evaluation of bone availability in the cleft area following secondary osteoplasty. J Craniomaxillofac Surg 2006;34(Suppl 2):57-61.
Gimbel M, Ashley RK, Sisodia M, Gabbay JS, Wasson KL, Heller J, et al
. Repair of alveolar cleft defects: Reduced morbidity with bone marrow stem cells in a resorbable matrix. J Craniofac Surg 2007;18:895-901.
Moreu JL, Caccamese JF, Coletti DP, Sauk JJ, Fisher JP. Tissue engineering solutions for cleft palates. J Oral Maxillofac Surg 2007;65:2503-11.
Dheeraj K, Rastogi N, Singh M. Modern practice in orthognathic and reconstructive surgery- craniofacial distraction osteogenesis. J Public Health Epidemiol 2011;3:129-37.
Cetrulo CL Jr, Knox KR, Brown DJ, Ashinoff RL, Dobryansky M, Ceradini DJ, et al
. Stem cells and distraction osteogenesis: Endothelial progenitor cells home to the ischemic generate in activation and consolidation. Plast Reconstr Surg 2005;116:1053-67.
Qi M, Hu J, Zou S, Zhou H, Han L. Mandibular distraction osteogenesis enhanced by bone marrow mesenchymal stem cells in rats. J Craniomaxillofac Surg 2006;34:283-9.
Lai QG, Yaun KF, Xu X, Li DR, Li GJ, Wei FL, et al
. Transcription factor osterix modified bone marrow mesenchymal stem cells enhance callus formation during distraction osteogenesis. Oral Surg Med Oral Pathol Oral Radiol Endod 2011;111:412-9.
Okeson JP. Orofacial Pain: Guidelines for Assessment, Diagnosis and Management. 3 rd
ed. Carol Stream, IL: Quintessence Publishing Co. Inc.; 1996. p. 1-15.
Ta LE, Phero JC, Pillemer SR, Hale-Donze H, McCartney-Francis N, Kingman A, et al
. Clinical evaluation of patients with temporomandibular joint implants. J Oral Maxillofac Surg 2002;60:1389-99.
Yaun K, Lee T, Huang J. Temporomandibular joint reconstruction: From alloplastic prosthesis to bioengineering tissue. J Med Biol Eng 2010;30:65-72.
Bailey MM, Wang L, Bode CJ, Mitchell KE, Detamore MS. A comparison of human umbilical cord matrix stem cells and temporomandibular joint condylar chondrocytes for tissue engineering temporomandibular joint condylar cartilage. Tissue Eng 2007;13:2003-10.
Schek RM, Taboas JM, Hollister SJ, Krebsbach PH. Tissue engineering osteochondral implants for temporomandibular joint repair. Orthod Craniofac Res 2005;8:313-9.
Alhadlaq A, Mao JJ. Tissue-engineered neogenesis of human-shaped mandibular condyle from rat mesenchymal stem cells. J Dent Res 2003;82:951-6.
Alhadlaq A, Mao JJ. Tissue-engineered osteochondral constructs in the shape of an articular condyle. J Bone Joint Surg Am 2005;87:936-44.
Alhadlaq A, Elisseeff JH, Hong L, Williams CG, Caplan AI, Sharma B, et al
. Adult stem cell driven genesis of human-shaped articular condyle. Ann Biomed Eng 2004;32:911-23.
Mao JJ. Calvarial development: Cells and mechanics. Curr Opin Orthop 2005;16:331-7.
Dudas JR, Marra KG, Cooper GM, Penascino VM, Mooney MP, Jiang S, et al
. The osteogenic potential of adipose-derived stem cells for the repair of rabbit calvarial defects. Ann Plast Surg 2006;56:543-8.
Yoon E, Dhar S, Chun DE, Gharibjanian NA, Evans GR. In vivo
osteogenic potential of human adipose-derived stem cells/poly lactide-co-glycolic acid constructs for bone regeneration in a rat critical-sized calvarial defect model. Tissue Eng 2007;13:619-27.
|This article has been cited by|
||Osteoclastic effects of mBMMSCs under compressive pressure during orthodontic tooth movement
| ||Jing Wang,Delong Jiao,Xiaofeng Huang,Yuxing Bai |
| ||Stem Cell Research & Therapy. 2021; 12(1) |
|[Pubmed] | [DOI]|
||Applications of stem cells in orthodontics and dentofacial orthopedics: Current trends and future perspectives
| ||Shiva Safari,Arezoo Mahdian,Saeed Reza Motamedian |
| ||World Journal of Stem Cells. 2018; 10(6): 66 |
|[Pubmed] | [DOI]|
||Changing Paradigms in Cranio-Facial Regeneration: Current and New Strategies for the Activation of Endogenous Stem Cells
| ||Luigi Mele,Pietro Paolo Vitiello,Virginia Tirino,Francesca Paino,Alfredo De Rosa,Davide Liccardo,Gianpaolo Papaccio,Vincenzo Desiderio |
| ||Frontiers in Physiology. 2016; 7 |
|[Pubmed] | [DOI]|