Literature DB >> 10321215

Biological mediators for periodontal regeneration.

D L Cochran1, J M Wozney.   

Abstract

A review of the literature on the use of growth-regulatory molecules in the oral cavity permits a model in which to consider approaches to oral tissue engineering. These concepts apply to periodontal regeneration and to regeneration of alveolar bone. In either case, the formation of tissues is complex but proceeds in a deliberate and orderly sequence. In these sequence of events resulting in either bone or cementum formation, periodontal ligament and bone can be stimulated at various points. Different signals can apparently be used to stimulate tissue formation including mitogenic signals and differentiation factors. Additionally, both hard and soft tissue stimulatory molecules appear to be permissive. Classic receptor-mediated peptides or extracellular matrix molecules for soft and hard tissues appear to allow stimulation of tissue formation cascades. Importantly, it also appears that the stimulatory event is transitory (that is, short-lived) and leads itself to a sequence of cellular events. These cellular events in turn stimulate a number of subsequent events (such as chemotaxis, proliferation, differentiation or angiogenesis), which lead to further progression of tissue formation. While a solid scientific rationale exists for the use of a variety of growth and attachment factors in regeneration of oral tissues, only a small number are being pursued clinically. Many therapeutic regimens have failed in preclinical testing or have resulted in limited regenerative capacity. The mitogenic polypeptides that stimulate soft tissue growth (such as platelet-derived growth factor) and both hard and soft tissue growth (such as transforming growth factor-beta) appear to have not led to successful enough outcomes to facilitate further work towards regulatory approval. The demonstrated ability of bone morphogenetic proteins to generate substantial quantities of bone suggest many applications in the oral cavity where this is the only tissue desired. Another therapeutic candidate is enamel matrix derivative, a set of matrix proteins. Enamel matrix derivative appears to stimulate first acellular cementum formation, which may allow for functional periodontal ligament formation. It will be of interest in the future to determine whether the protein matrix contains classic mitogenic or differentiation factors as well as the amelogenins. It is also evident that the bone morphogenetic proteins permit periodontal ligament formation. The conditions for stimulating predictable periodontal ligament tissues with bone morphogenetic proteins however are not known. It is clear that the bone morphogenetic proteins are excellent molecules for stimulating oral bone formation. The results of all these studies will determine the future therapeutic potential for these growth molecules such that they may be used to optimally stimulate and direct specific points along tissue formation cascades.

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Year:  1999        PMID: 10321215     DOI: 10.1111/j.1600-0757.1999.tb00146.x

Source DB:  PubMed          Journal:  Periodontol 2000        ISSN: 0906-6713            Impact factor:   7.589


  35 in total

1.  Effect of PDGF-BB combined with EDTA gel on adhesion and proliferation to the root surface.

Authors:  Mahmoud Helmy Belal; Hisashi Watanabe; Shizuko Ichinose; Isao Ishikawa
Journal:  Odontology       Date:  2012-01-17       Impact factor: 2.634

2.  Excessıve fluorıde ıntake alters the MMP-2, TIMP-1 and TGF-β levels of perıodontal soft tıssues: an experımental study ın rabbıts.

Authors:  Müge Lütfioğlu; Elif Eser Sakallıoğlu; Umur Sakallıoğlu; M Yavuz Gülbahar; Mehtap Muğlalı; Burcu Baş; Abdurrahman Aksoy
Journal:  Clin Oral Investig       Date:  2011-12-07       Impact factor: 3.573

3.  Non-thermal atmospheric pressure plasma increased mRNA expression of growth factors in human gingival fibroblasts.

Authors:  Jae-Sung Kwon; Yong Hee Kim; Eun Ha Choi; Chong-Kwan Kim; Kyoung-Nam Kim; Kwang-Mahn Kim
Journal:  Clin Oral Investig       Date:  2015-11-27       Impact factor: 3.573

Review 4.  Regeneration therapy for oral disease.

Authors:  Kyuichi Kamoi; Masako Iino; Hitomi Ishiguro
Journal:  Hum Cell       Date:  2006-05       Impact factor: 4.174

Review 5.  Gene therapeutics for periodontal regenerative medicine.

Authors:  Christoph A Ramseier; Zachary R Abramson; Qiming Jin; William V Giannobile
Journal:  Dent Clin North Am       Date:  2006-04

Review 6.  The effect of platelet-rich plasma on clinical outcomes of the surgical treatment of periodontal intrabony defects: A systematic review and meta-analysis.

Authors:  Xinshan Hou; Jingwen Yuan; Absijiang Aisaiti; Yuan Liu; Jin Zhao
Journal:  BMC Oral Health       Date:  2016-08-17       Impact factor: 2.757

Review 7.  Bone repair cells for craniofacial regeneration.

Authors:  G Pagni; D Kaigler; G Rasperini; G Avila-Ortiz; R Bartel; W V Giannobile
Journal:  Adv Drug Deliv Rev       Date:  2012-03-10       Impact factor: 15.470

8.  FGF2 gene activated matrices promote proliferation of bone marrow stromal cells.

Authors:  Sheetal D'Mello; Satheesh Elangovan; Aliasger K Salem
Journal:  Arch Oral Biol       Date:  2015-09-09       Impact factor: 2.633

9.  Inactivation of epidermal growth factor by Porphyromonas gingivalis as a potential mechanism for periodontal tissue damage.

Authors:  Krzysztof Pyrc; Aleksandra Milewska; Tomasz Kantyka; Aneta Sroka; Katarzyna Maresz; Joanna Kozieł; Ky-Anh Nguyen; Jan J Enghild; Anders Dahl Knudsen; Jan Potempa
Journal:  Infect Immun       Date:  2012-10-22       Impact factor: 3.441

10.  The effect of different platelet-rich plasma concentrations on proliferation and differentiation of human periodontal ligament cells in vitro.

Authors:  J Han; H X Meng; J M Tang; S L Li; Y Tang; Z B Chen
Journal:  Cell Prolif       Date:  2007-04       Impact factor: 6.831

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