Following are some abstracts of recent advances in medical research on dental pulp stem cells
Braz Dent J. 2011;22(2):91-8.
Mesenchymal stem cells in the dental tissues: perspectives for tissue regeneration.
Estrela C, Alencar AH, Kitten GT, Vencio EF, Gava E. Dental School, Federal University of Goiás, Goiânia, GO, Brazil.
In recent years, stem cell research has grown exponentially owing to the recognition that stem cell-based therapies have the potential to improve the life of patients with conditions that range from Alzheimer's disease to cardiac ischemia and regenerative medicine, like bone or tooth loss. Based on their ability to rescue and/or repair injured tissue and partially restore organ function, multiple types of stem/progenitor cells have been speculated. Growing evidence demonstrates that stem cells are primarily found in niches and that certain tissues contain more stem cells than others. Among these tissues, the dental tissues are considered a rich source of mesenchymal stem cellsthat are suitable for tissue engineering applications. It is known that these stem cells have the potential to differentiate into several cell types, including odontoblasts, neural progenitors, osteoblasts, chondrocytes, and adipocytes. In dentistry, stem cell biology and tissue engineering are of great interest since may provide an innovative for generation of clinical material and/or tissue regeneration. Mesenchymal stem cells were demonstrated in dental tissues, including dental pulp, periodontal ligament, dentalpapilla, and dental follicle. These stem cells can be isolated and grown under defined tissue culture conditions, and are potential cells for use in tissue engineering, including, dental tissue, nerves and bone regeneration. More recently, another source of stem cell has been successfully generated from human somatic cells into a pluripotent stage, the induced pluripotent stem cells (iPS cells), allowing creation of patient- and disease-specific stem cells. Collectively, the multipotency, high proliferation rates, and accessibility make the dental stem cell an attractive source of mesenchymal stem cells for tissue regeneration. This review describes new findings in the field ofdental stem cell research and on their potential use in the tissue regeneration.
Stem cells, 2009 Sep; 27(9):2229-37
Implanted adult human dental pulp stem cells induce endogenous axon guidance
Arthur A, Shi S,Zannettino AC, Fujii N, Gronthos s, Koblar SA,
Mesenchymal Stem Cell Group, CSCR University of Adelaide, Adelaide, South
The human central nervous system has a limited capacity for regeneration. Stem cell-based therapies may overcome this through cellular mechanisms of neural replacement and/or through molecular mechanisms, whereby secreted factors induce change in the host tissue. To investigate these mechanisms, we used a readily accessible human cell population, dental pulp progenitor/stem cells (DPSCs) that can differentiate into functionally active neurons given the appropriate environmental cues. We hypothesized that implanted DPSCs secrete factors that coordinate axon guidance within a receptive host nervous system. An avian embryonic model system was adapted to investigate axon guidance in vivo after transplantation of adult human DPSCs. Chemoattraction of avian trigeminal ganglion axons toward implanted DPSCs was mediated via the chemokine, CXCL12, also known as stromal cell-derived factor-1, and its receptor, CXCR4. These findings provide the first direct evidence that DPSCs may induce neuroplasticity within a receptive host nervous system
J Clin Pediatr Dent. 2009 Summer;33(4):289-94
Banking stem cells from human exfoliated deciduous teeth (SHED) saving for the future
Arora V, Arora P, Munshi AK. Department of Conservative Dentistry and Endodontics, K.D. Dental College and Hospital, Mathura, India.
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
Tooth derived cells are readily accessible and provide an easy and minimally invasive way to obtain and store stem cells for future use. Banking one’s own tooth-derived stem cells are a reasonable and simple alternative to harvesting stem cells from other tissues. Obtaining stem cells from human exfoliated deciduous teeth (SHED) is simple and convenient, with little or no trauma. Every child loses primary teeth, which creates the perfect opportunity to recover and store this convenient source of stem cells--should they be needed to treat future injuries or ailments and presents a far better alternative to simply discarding the teeth or storing them as mementos from the past. Furthermore, using ones own stem cells poses few, if any, risks for developing immune reactions or rejection following transplantation and also eliminates the potential of contracting disease from donor cells.
Stem cells can also be recovered from developing wisdom teeth and permanent teeth. Individuals have different opportunities at different stages of their life to bank these valuable cells. It is best to recover stem cells when a child is young and healthy and the cells are strong and proliferative.
The purpose of this review is to discuss the present scenario as well as the technical details of tooth banking as related to SHED cells.
J Contemp Dent Pract. 2009 Jul 1;10(4):90-6
Stem cells: therapeutic potential in dentistry.
Arora V, Arora P, Munshi AK. Nedel F, André Dde A, de Oliveira IO, Cordeiro MM, Casagrande L, Tarquinio SB, Nor JE, Demarco FF. School of Dentistry, Federal University of Pelotas, Pelotas, RS, Brazil.
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
AIM: The aim of this paper is to present a review and discussion of the current status of stem cell research with regard to tooth generation.
BACKGROUND: Stem cells have been isolated from the pulp tissue of both deciduous and permanent teeth as well as from the periodontal ligament. Dental pulp stem cells demonstrate the capacity to form a dentin pulp-like complex in immunocompromised mice. A tooth-like structure was successfully formed, using a heterogeneous mixture of dental enamel epithelium, pulp mesenchymal cells, and scaffolds.
CONCLUSION: The scientific community understands the need for more investigations to completely understand the conditions that would best favor the creation of a tooth substitute. Recent gains in the understanding of the molecular regulation of tooth morphogenesis, stem cell biology, and biotechnology offers the opportunity to realize this goal.
CLINICAL SIGNIFICANCE: These findings, combined with the recent progress in stem cell research and tissue engineering, might allow the development of alternatives for current materials and therapies used to treat tooth tissue loss (e.g., enamel, dentin, pulp), reconstruct dentoalveolar and craniofacial bone defects, and eventually replace an entire tooth.
Nan Fang Yi Ke Da Xue Xue Bao. 2009 Mar;29(3):479-82
Isolation and identification of stem cells derived from human exfoliated deciduous teeth.
Xu N, Chen K, Shen YY. Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
OBJECTIVE: To isolate and identify stem cells from human exfoliated deciduous teeth (SHED).
METHODS: Human pulp tissue were dissected and digested to obtain the single cell suspension. The cell morphology was observed and the clonality of the obtained cells was assessed. The phenotype of the cells was detected by immunohistochemistry and flow cytometry (FCM), and the cell cycle was analyzed. The in vitro differentiation of the cells into adipose tissue and formation of mineralization nodules were evaluated.
RESULTS: Clonogenic assay showed the formation of 16-18 clones in every 10(3) plated cells derived from human exfoliated deciduous teeth. These cells were found to express the markers of mesenchymal stem cells with a multipotent differentiation potential.
CONCLUSION: The cells isolated from human dental pulp are clonogenic and have multipotent differentiation potential, suggesting their identity of SHED.
Stem Cells. 2008 Jul;26(7):1787-95. Epub 2008 May 22.
Adult human dental pulp stem cells differentiate toward functionally active neurons under appropriate environmental cues.
Arthur A, Rychkov G, Shi S, Koblar SA, Gronthos S. The Australian Research Council, Centre for the Molecular Genetics of Development, University of Adelaide, Adelaide, Australia.
Human adult dental pulp stem cells (DPSCs) reside within the perivascular niche of dental pulp and are thought to originate from migrating cranial neural crest (CNC) cells. During embryonic development, CNC cells differentiate into a wide variety of cell types, including neurons of the peripheral nervous system. Previously, we have demonstrated that DPSCs derived from adult human third molar teeth differentiate into cell types reminiscent of CNC embryonic ontology.
We hypothesized that DPSCs exposed to the appropriate environmental cues would differentiate into functionally active neurons. The data demonstrated that ex vivo-expanded human adult DPSCs responded to neuronal inductive conditions both in vitro and in vivo. Human adult DPSCs, but not human foreskin fibroblasts (HFFs), acquired a neuronal morphology, and expressed neuronal-specific markers at both the gene and protein levels. Culture-expanded DPSCs also exhibited the capacity to produce a sodium current consistent with functional neuronal cells when exposed to neuronal inductive media.
Furthermore, the response of human DPSCs and HFFs to endogenous neuronal environmental cues was determined in vivo using an avian xenotransplantation assay. DPSCs expressed neuronal markers and acquired a neuronal morphology following transplantation into the mesencephalon of embryonic day-2 chicken embryo, whereas HFFs maintained a thin spindle fibroblastic morphology. We propose that adult human DPSCs provide a readily accessible source of exogenous stem/precursor cells that have the potential for use in cell-therapeutic paradigms to treat neurological disease.
J Endod. 2008 Jun;34(6):645-51.
The hidden treasure in apical papilla: the potential role in pulp/dentin regeneration and bioroot engineering.
Huang GT, Sonoyama W, Liu Y, Liu H, Wang S, Shi S. University of Maryland, College of Dental Surgery, Dental School, Department of Endodontics, Prosthodontics and Operative Dentistry, Baltimore, Maryland 21201, USA.
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
Some clinical case reports have shown that immature permanent teeth with periradicular periodontitis or abscess can undergo apexogenesis after conservative endodontic treatment.
A call for a paradigm shift and new protocol for the clinical management of these cases has been brought to attention.
Concomitantly, a new population of mesenchymal stem cells residing in the apical papilla of permanent immature teeth recently has been discovered and was termed stem cells from the apical papilla (SCAP). These stem cells appear to be the source of odontoblasts that are responsible for the formation of root dentin.
Conservation of these stem cells when treating immature teeth may allow continuous formation of the root to completion.
This article reviews current findings on the isolation and characterization of these stem cells. The potential role of these stem cells in the following respects will be discussed: (1) their contribution in continued root maturation in endodontically treated immature teeth with periradicular periodontitis or abscess and (2) their potential utilization for pulp/dentin regeneration and bioroot engineering.