Literature DB >> 28844306

Signaling Molecules and Pulp Regeneration.

Gottfried Schmalz1, Matthias Widbiller2, Kerstin M Galler2.   

Abstract

Signaling molecules play an essential role in tissue engineering because they regulate regenerative processes. Evidence exists from animal studies that single molecules such as members of the transforming growth factor beta superfamily and factors that induce the growth of blood vessels (vascular endothelial growth factor), nerves (brain-derived neurotrophic factor), or fibroblasts (fibroblast growth factor) may induce reparative dentin formation. Mainly the formation of atubular dentin (osteodentin) has been described after the application of single molecules or combinations of recombinant growth factors on healthy exposed pulps or in pulp regeneration. Generally, such preparations have not received regulatory approval on the market so far. Only the use of granulocyte colony-stimulating factors together with cell transplantation is presently tested clinically. Besides approaches with only 1 or few combined molecules, the exploitation of tissue-derived growth factors depicts a third promising way in dental pulp tissue engineering. Preparations such as platelet-rich plasma or platelet-rich fibrin provide a multitude of endogenous signaling molecules, and special regulatory approval for the market does not seem necessary. Furthermore, dentin is a perfect reservoir of signaling molecules that can be mobilized by treatment with demineralizing agents such as EDTA. This conditions the dentin surface and allows for contact differentiation of pulp stem cells into odontoblastlike cells, protects dentin from resorption, and enhances cell growth as well as attachment to dentin. By ultrasonic activation, signaling molecules can be further released from EDTA pretreated dentin into saline, thus avoiding cytotoxic EDTA in the final preparation. The use of dentin-derived growth factors offers a number of advantages because they are locally available and presumably are most fit to induce signaling processes in dental pulp. However, better characterization and standardization of the procedures are required.
Copyright © 2017 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dental pulp tissue engineering; dentin matrix proteins; growth factors; pulp regeneration; scaffold

Mesh:

Substances:

Year:  2017        PMID: 28844306     DOI: 10.1016/j.joen.2017.06.003

Source DB:  PubMed          Journal:  J Endod        ISSN: 0099-2399            Impact factor:   4.171


  5 in total

Review 1.  Challenges of Engineering Biomimetic Dental and Paradental Tissues.

Authors:  Mohammed E Grawish; Lamyaa M Grawish; Hala M Grawish; Mahmoud M Grawish; Salwa A El-Negoly
Journal:  Tissue Eng Regen Med       Date:  2020-07-03       Impact factor: 4.169

Review 2.  Endodontic regeneration: hard shell, soft core.

Authors:  Matthias Widbiller; Gottfried Schmalz
Journal:  Odontology       Date:  2020-12-02       Impact factor: 2.634

Review 3.  Inflammatory Response Mechanisms of the Dentine-Pulp Complex and the Periapical Tissues.

Authors:  Kerstin M Galler; Manuel Weber; Yüksel Korkmaz; Matthias Widbiller; Markus Feuerer
Journal:  Int J Mol Sci       Date:  2021-02-02       Impact factor: 5.923

4.  Impact of remnant healthy pulp and apical tissue on outcomes after simulated regenerative endodontic procedure in rat molars.

Authors:  Naoki Edanami; Kunihiko Yoshiba; Mari Shirakashi; Razi Saifullah Ibn Belal; Nagako Yoshiba; Naoto Ohkura; Aiko Tohma; Ryosuke Takeuchi; Takashi Okiji; Yuichiro Noiri
Journal:  Sci Rep       Date:  2020-12-01       Impact factor: 4.379

Review 5.  Biomolecule-Mediated Therapeutics of the Dentin-Pulp Complex: A Systematic Review.

Authors:  Foteini Machla; Ioannis Angelopoulos; Matthias Epple; Maria Chatzinikolaidou; Athina Bakopoulou
Journal:  Biomolecules       Date:  2022-02-09
  5 in total

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