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Dr. Ashok Ayer
Department of Conservative Dentistry &
Endodontics
CODS, BPKIHS, Dharan
Introduction
 Regenerative endodontics: is a biologically based

procedure designed to replace damaged structures,
Dentin and root structures
Cells of the pulp-dentin complex
 Vital pulp therapy with pulp stem/progenitor cells

might regenerate dentin-pulp complex without the
removal of the whole pulp.
 Caries, pulpitis, and apical periodontitis ultimately

result in premature tooth
diminishing the quality of life

loss

and

therefore

 Regeneration of parts of the tooth structure can

prevent or delay the loss of the whole tooth.
The key ingredients for tissue engineering [1].
Proteins that bind on receptors
on the cell and induce cellular
proliferation & differentiation.

The major domains of research required to develop regenerative endodontic procedures.
 Stem cell: ability to;

Continuously divide to either replicate itself
(self-renewing),
or
Produce specialized cells than can differentiate into
various other types of cells or tissues
(multilineage differentiation)
 Embryonic stem cells derive from the early mammalian

embryo at the blastocyst stage and have the capability to
give rise to all kinds of cells.(Pluripotent)
 Adult /Postnatal stem cells are just multipotent

because their differentiation potential is restricted to
certain cell lineages
DPSCs: multipotency, high proliferation rates and accessibility (2)

(Gronthos et al., 2000) (3)
(Miura et al., 2003) (4)
(Seo et al., 2004) (5)

[6]
The scaffold provides a 3D environment
for cells to attach and grow,
(Therefore mimicking the in vivo
condition)

collagen, gelatin, dextran and fibronectin.

Polylactic acid (PLA),
Polyglycolic acid (PGA),
Poly lactic-co-glycolic acid (PLGA

/Growth factors
The key elements of tissue engineering and dentin regeneration

[7]
 Laino and co-workers [8] isolated a selected
subpopulation of DPSCs called;

Stromal bone producing dental pulp stem cells
(SBP-DPSCs)
Which roughly represent 10% of dental pulp cells
 These cells display a great capability of selfexpanding and differentiating in pre-osteoblasts;

which are able to self-maintain and renew for long
time.
Role of DPSCs in regenerative dentistry
Pulp tissue is exposed
I. Calcium hydroxide and mineral trioxide aggregate
(MTA), promotes the activity of reparative
dentinogenesis
II. Bigger traumas or advanced caries are clinically treated
with root canal therapy.
III. Regenerative approaches:

In which diseased or necrotic pulp tissues are removed
and
Replaced with regenerated pulp tissues
To revitalize the teeth.
The two main strategies for pulp therapy to regenerate dentin: in vivo and ex vivo
methods by application of BMP gene. [7]
Dentin-pulp complex formation with optimal orientation for clinical application of regenerative therapy. The pulp
stem cells are transduced with BMP gene and attached to a defined scaffold to differentiate into odontoblasts. The
tubular dentin-pulp complex can be transplanted on the exposed or amputated pulp in the cavity. [9]
Developmental approaches for regenerative endodontic
techniques [1]
(J Endod 2007;33:377-90)
Ikeda et al. (2009)
Reported a successful fully functioning tooth replacement in an adult mouse
achieved through the transplantation of bioengineered tooth germ into the alveolar
bone in the lost tooth region.
Conclusion:
These results together raise the possibility that a
protocol for pulp tissue regeneration and new dentin
formation for clinical therapeutic purposes could be
established.
It may offer an alternative approach to save teeth that
may have compromised structural integrity.
References:
1.

2.

3.

4.

Peter E. Murray et al. Regenerative endodontics: A review of current
status and a call for action J Endod 2007;33:377-90.
doi:1o.1016/j.joen.2006.09.013
Yamada, Y., Ito, K., Nakamura, S., Ueda, M. & Nagasaka, T. (2010).
Promising cell-based therapy for bone regeneration using stem cells
from deciduous teeth, dental pulp, and bone marrow. Cell
Transplantation. (October 2010)
Gronthos, S., Mangani, M., Brahim, J., Robey, PG. & Shi, S. (2000).
Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo.
Proceedings of the National Academy of Sciences of the United States
of America, Vol.97, No.25, (December 2000), pp. 13625- 13630, ISSN
0027-8424
Miura, M., Gronthos, S., Zhao, M., Lu, B., Fisher, LW., Robey, PG. &
Shi, S. (2003). SHED: stem cells from human exfoliated deciduous
teeth. Proceedings of the National Academy of Sciences of the United
Stases of America, Vol.100, No.10, (May 2003), pp.5807-5812, ISSN
0027-8424
5. Seo, BM., Miura, M., Gronthos, S., Bartold, PM., Batouli, S., Brahim, J.,

Young, M., Robey,PG., Wang, CY. & Shi, S. (2004). Investigation of
multipotent postnatal stem cells from human periodontal ligament.
Lancet, Vol.364, No.9429, (July 2004), pp.149-155, ISSN 0140-6736
6. George T.-J. Huang Dental pulp and dentin tissue engineering and
regeneration: advancement and challenge Frontiers in Bioscience E3,
788-800, January 1, 2011
7. Nakashima M. Bone morphogenetic proteins in dentin regeneration
for potential use in endodontic therapy. Cytokine growth factor Rev.
2005;16(3):369-76
8. Laino, G., D'Aquino, R., Graziano, A., Lanza, V., Carinci, F., Naro, F.,
Pirozzi, G., & Papaccio, G. (2005). A new population of human adult
dental pulp stem cells: a useful source of living autologous fibrous
bone tissue (LAB). Journal of Bone and Mineral Research, Vol.20,
No.8, (August 2005), pp.1394-1402, ISSN 0884-0431
9. The Application of Tissue Engineering to Regeneration of Pulp and
Dentin in Endodontics Misako Nakashima, PhD, DDS, and Akifumi
Akamine, PhD, DDS
10. Nakashima, M. (2005). Bone morphogenetic proteins in dentin
regeneration for potential use in endodontic therapy. Cytokine &
Growth Factor Reviews, Vol.16, No.3, (June 2005), pp.369-376 ISSN
1359-6101
11. Paul C Edwards et al. Gene-enhanced tissue engineering for dental
hard tissue regeneration: (2) dentin-pulp and periodontal
regeneration. Head & Face Medicine 2006, 2:16 . doi:10.1186/1746-160X2-16
12. D’aquino R, De Rosa A, Laino G, Caruso F, Guida L, Rullo R, Checchi V,
Laino L, Tirino V, Papaccio G. 2008. Human dental pulp stem cells:
from biology to clinical applications. J. Exp. Zool. (Mol. Dev. Evol.) 310B
13. Ikeda E, Morita R, Nakao K, Ishida K, Nakamura T, Takano-Yamamoto
T et al. Fully functional bioengineered tooth replacement as an organ
replacement therapy. Proc Natl Acad Sci USA. 2009 Aug;106(32):1347580.
Expanding therapeutic boundaries: Regenerative Endodontics

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Expanding therapeutic boundaries: Regenerative Endodontics

  • 1. Dr. Ashok Ayer Department of Conservative Dentistry & Endodontics CODS, BPKIHS, Dharan
  • 2. Introduction  Regenerative endodontics: is a biologically based procedure designed to replace damaged structures, Dentin and root structures Cells of the pulp-dentin complex  Vital pulp therapy with pulp stem/progenitor cells might regenerate dentin-pulp complex without the removal of the whole pulp.
  • 3.  Caries, pulpitis, and apical periodontitis ultimately result in premature tooth diminishing the quality of life loss and therefore  Regeneration of parts of the tooth structure can prevent or delay the loss of the whole tooth.
  • 4. The key ingredients for tissue engineering [1]. Proteins that bind on receptors on the cell and induce cellular proliferation & differentiation. The major domains of research required to develop regenerative endodontic procedures.
  • 5.  Stem cell: ability to; Continuously divide to either replicate itself (self-renewing), or Produce specialized cells than can differentiate into various other types of cells or tissues (multilineage differentiation)  Embryonic stem cells derive from the early mammalian embryo at the blastocyst stage and have the capability to give rise to all kinds of cells.(Pluripotent)  Adult /Postnatal stem cells are just multipotent because their differentiation potential is restricted to certain cell lineages
  • 6. DPSCs: multipotency, high proliferation rates and accessibility (2) (Gronthos et al., 2000) (3) (Miura et al., 2003) (4) (Seo et al., 2004) (5) [6]
  • 7. The scaffold provides a 3D environment for cells to attach and grow, (Therefore mimicking the in vivo condition) collagen, gelatin, dextran and fibronectin. Polylactic acid (PLA), Polyglycolic acid (PGA), Poly lactic-co-glycolic acid (PLGA /Growth factors The key elements of tissue engineering and dentin regeneration [7]
  • 8.  Laino and co-workers [8] isolated a selected subpopulation of DPSCs called; Stromal bone producing dental pulp stem cells (SBP-DPSCs) Which roughly represent 10% of dental pulp cells  These cells display a great capability of selfexpanding and differentiating in pre-osteoblasts; which are able to self-maintain and renew for long time.
  • 9. Role of DPSCs in regenerative dentistry Pulp tissue is exposed I. Calcium hydroxide and mineral trioxide aggregate (MTA), promotes the activity of reparative dentinogenesis II. Bigger traumas or advanced caries are clinically treated with root canal therapy. III. Regenerative approaches: In which diseased or necrotic pulp tissues are removed and Replaced with regenerated pulp tissues To revitalize the teeth.
  • 10. The two main strategies for pulp therapy to regenerate dentin: in vivo and ex vivo methods by application of BMP gene. [7]
  • 11. Dentin-pulp complex formation with optimal orientation for clinical application of regenerative therapy. The pulp stem cells are transduced with BMP gene and attached to a defined scaffold to differentiate into odontoblasts. The tubular dentin-pulp complex can be transplanted on the exposed or amputated pulp in the cavity. [9]
  • 12. Developmental approaches for regenerative endodontic techniques [1] (J Endod 2007;33:377-90)
  • 13.
  • 14.
  • 15. Ikeda et al. (2009) Reported a successful fully functioning tooth replacement in an adult mouse achieved through the transplantation of bioengineered tooth germ into the alveolar bone in the lost tooth region.
  • 16. Conclusion: These results together raise the possibility that a protocol for pulp tissue regeneration and new dentin formation for clinical therapeutic purposes could be established. It may offer an alternative approach to save teeth that may have compromised structural integrity.
  • 17. References: 1. 2. 3. 4. Peter E. Murray et al. Regenerative endodontics: A review of current status and a call for action J Endod 2007;33:377-90. doi:1o.1016/j.joen.2006.09.013 Yamada, Y., Ito, K., Nakamura, S., Ueda, M. & Nagasaka, T. (2010). Promising cell-based therapy for bone regeneration using stem cells from deciduous teeth, dental pulp, and bone marrow. Cell Transplantation. (October 2010) Gronthos, S., Mangani, M., Brahim, J., Robey, PG. & Shi, S. (2000). Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proceedings of the National Academy of Sciences of the United States of America, Vol.97, No.25, (December 2000), pp. 13625- 13630, ISSN 0027-8424 Miura, M., Gronthos, S., Zhao, M., Lu, B., Fisher, LW., Robey, PG. & Shi, S. (2003). SHED: stem cells from human exfoliated deciduous teeth. Proceedings of the National Academy of Sciences of the United Stases of America, Vol.100, No.10, (May 2003), pp.5807-5812, ISSN 0027-8424
  • 18. 5. Seo, BM., Miura, M., Gronthos, S., Bartold, PM., Batouli, S., Brahim, J., Young, M., Robey,PG., Wang, CY. & Shi, S. (2004). Investigation of multipotent postnatal stem cells from human periodontal ligament. Lancet, Vol.364, No.9429, (July 2004), pp.149-155, ISSN 0140-6736 6. George T.-J. Huang Dental pulp and dentin tissue engineering and regeneration: advancement and challenge Frontiers in Bioscience E3, 788-800, January 1, 2011 7. Nakashima M. Bone morphogenetic proteins in dentin regeneration for potential use in endodontic therapy. Cytokine growth factor Rev. 2005;16(3):369-76 8. Laino, G., D'Aquino, R., Graziano, A., Lanza, V., Carinci, F., Naro, F., Pirozzi, G., & Papaccio, G. (2005). A new population of human adult dental pulp stem cells: a useful source of living autologous fibrous bone tissue (LAB). Journal of Bone and Mineral Research, Vol.20, No.8, (August 2005), pp.1394-1402, ISSN 0884-0431 9. The Application of Tissue Engineering to Regeneration of Pulp and Dentin in Endodontics Misako Nakashima, PhD, DDS, and Akifumi Akamine, PhD, DDS 10. Nakashima, M. (2005). Bone morphogenetic proteins in dentin regeneration for potential use in endodontic therapy. Cytokine & Growth Factor Reviews, Vol.16, No.3, (June 2005), pp.369-376 ISSN 1359-6101
  • 19. 11. Paul C Edwards et al. Gene-enhanced tissue engineering for dental hard tissue regeneration: (2) dentin-pulp and periodontal regeneration. Head & Face Medicine 2006, 2:16 . doi:10.1186/1746-160X2-16 12. D’aquino R, De Rosa A, Laino G, Caruso F, Guida L, Rullo R, Checchi V, Laino L, Tirino V, Papaccio G. 2008. Human dental pulp stem cells: from biology to clinical applications. J. Exp. Zool. (Mol. Dev. Evol.) 310B 13. Ikeda E, Morita R, Nakao K, Ishida K, Nakamura T, Takano-Yamamoto T et al. Fully functional bioengineered tooth replacement as an organ replacement therapy. Proc Natl Acad Sci USA. 2009 Aug;106(32):1347580.