Redefining the induction of periodontal tissue regeneration in primates by the osteogenic proteins of the transforming growth factor-β supergene family
- PMID: 26833268
- DOI: 10.1111/jre.12356
Redefining the induction of periodontal tissue regeneration in primates by the osteogenic proteins of the transforming growth factor-β supergene family
Abstract
The molecular bases of periodontal tissue induction and regeneration are the osteogenic proteins of the transforming growth factor-β (TGF-β) supergene family. These morphogens act as soluble mediators for the induction of tissues morphogenesis sculpting the multicellular mineralized structures of the periodontal tissues with functionally oriented ligament fibers into newly formed cementum. Human TGF-β3 (hTGF-β3 ) in growth factor-reduced Matrigel® matrix induces cementogenesis when implanted in class II mandibular furcation defects surgically prepared in the non-human primate Chacma baboon, Papio ursinus. The newly formed periodontal ligament space is characterized by running fibers tightly attached to the cementoid surface penetrating as mineralized constructs within the newly formed cementum assembling and initiating within the mineralized dentine. Angiogenesis heralds the newly formed periodontal ligament space, and newly sprouting capillaries are lined by cellular elements with condensed chromatin interpreted as angioblasts responsible for the rapid and sustained induction of angiogenesis. The inductive activity of hTGF-β3 in Matrigel® matrix is enhanced by the addition of autogenous morcellated fragments of the rectus abdominis muscle potentially providing myoblastic, pericytic/perivascular stem cells for continuous tissue induction and morphogenesis. The striated rectus abdominis muscle is endowed with stem cell niches in para/perivascular location, which can be dominant, thus imposing stem cell features or stemness to the surrounding cells. This capacity to impose stemness is morphologically shown by greater alveolar bone induction and cementogenesis when hTGF-β3 in Matrigel® matrix is combined with morcellated fragments of autogenous rectus abdominis muscle. The induction of periodontal tissue morphogenesis develops as a mosaic structure in which the osteogenic proteins of the TGF-β supergene family singly, synergistically and synchronously initiate and maintain tissue induction and morphogenesis. In primates, the presence of several homologous yet molecularly different isoforms with osteogenic activity highlights the biological significance of this apparent redundancy and indicates multiple interactions during embryonic development and bone regeneration in postnatal life. Molecular redundancy with associated different biological functionalities in primate tissues may simply represent the fine-tuning of speciation-related molecular evolution in anthropoid apes at the early Pliocene boundary, which resulted in finer tuning of the bone induction cascade.
Keywords: bone morphogenetic proteins; periodontal tissue regeneration; primates; redundancy; transforming growth factor-β proteins.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Similar articles
-
Biological aspects of periodontal tissue regeneration: cementogenesis and the induction of Sharpey's fibres.SADJ. 2013 Aug;68(7):304-6, 308-12, 314 passim. SADJ. 2013. PMID: 24133950 Review.
-
Synergistic induction of periodontal tissue regeneration by binary application of human osteogenic protein-1 and human transforming growth factor-β3 in Class II furcation defects of Papio ursinus.J Periodontal Res. 2012 Jun;47(3):336-44. doi: 10.1111/j.1600-0765.2011.01438.x. Epub 2011 Dec 6. J Periodontal Res. 2012. PMID: 22142147
-
Induction of cementogenesis and periodontal ligament regeneration by recombinant human transforming growth factor-beta3 in Matrigel with rectus abdominis responding cells.J Periodontal Res. 2009 Feb;44(1):81-7. doi: 10.1111/j.1600-0765.2008.01086.x. Epub 2008 Oct 7. J Periodontal Res. 2009. PMID: 18973524
-
Developmental pathways of periodontal tissue regeneration: Developmental diversities of tooth morphogenesis do also map capacity of periodontal tissue regeneration?J Periodontal Res. 2019 Feb;54(1):10-26. doi: 10.1111/jre.12596. Epub 2018 Sep 12. J Periodontal Res. 2019. PMID: 30207395 Review.
-
Pleiotropism of bone morphogenetic proteins: from bone induction to cementogenesis and periodontal ligament regeneration.J Int Acad Periodontol. 2006 Jan;8(1):23-32. J Int Acad Periodontol. 2006. PMID: 16459886 Review.
Cited by
-
Carbon Monoxide Releasing Molecule-3 Enhances Osteogenic Differentiation of Human Periodontal Ligament Stem Cells by Carbon Monoxide Release.Drug Des Devel Ther. 2021 Apr 22;15:1691-1704. doi: 10.2147/DDDT.S300356. eCollection 2021. Drug Des Devel Ther. 2021. PMID: 33911854 Free PMC article.
-
Periodontal regeneration: Lessons from the periodontal ligament-cementum junction in diverse animal models.Front Dent Med. 2023 Mar 7;4:1124968. doi: 10.3389/fdmed.2023.1124968. eCollection 2023. Front Dent Med. 2023. PMID: 39916933 Free PMC article.
-
Evaluating the oxysterol combination of 22(S)-hydroxycholesterol and 20(S)-hydroxycholesterol in periodontal regeneration using periodontal ligament stem cells and alveolar bone healing models.Stem Cell Res Ther. 2017 Dec 6;8(1):276. doi: 10.1186/s13287-017-0725-9. Stem Cell Res Ther. 2017. PMID: 29208033 Free PMC article.
-
In Vitro Studies of Graphene for Management of Dental Caries and Periodontal Disease: A Concise Review.Pharmaceutics. 2022 Sep 21;14(10):1997. doi: 10.3390/pharmaceutics14101997. Pharmaceutics. 2022. PMID: 36297434 Free PMC article. Review.
-
Sequentially releasing self-healing hydrogel fabricated with TGFβ3-microspheres and bFGF to facilitate rat alveolar bone defect repair.Asian J Pharm Sci. 2022 May;17(3):425-434. doi: 10.1016/j.ajps.2022.03.003. Epub 2022 Apr 13. Asian J Pharm Sci. 2022. PMID: 35782329 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources