Events of wound healing/regeneration in the canine supraalveolar periodontal defect model

Aim The objective of this research was to elucidate early events in periodontal wound healing/regeneration using histological and immunohistochemical techniques. Methods Routine critical‐size, supraalveolar, periodontal defects including a space‐providing titanium mesh device were created in 12 dogs...

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Published inJournal of clinical periodontology Vol. 40; no. 5; pp. 527 - 541
Main Authors Dickinson, Douglas P., Coleman, Brandon G., Batrice, Nathan, Lee, Jaebum, Koli, Komal, Pennington, Cathy, Susin, Cristiano, Wikesjö, Ulf M. E.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.05.2013
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Summary:Aim The objective of this research was to elucidate early events in periodontal wound healing/regeneration using histological and immunohistochemical techniques. Methods Routine critical‐size, supraalveolar, periodontal defects including a space‐providing titanium mesh device were created in 12 dogs. Six animals received additional autologous blood into the defect prior to wound closure. One animal from each group was killed for analysis at 2, 5, 9, 14 days, and at 4 and 8 weeks. Results Both groups behaved similarly. Periodontal wound healing/regeneration progressed through three temporal phases. Early phase (2–5 days): heterogeneous clot consolidation and cell activation in the periodontal ligament (PDL) and trabecular bone was associated with PDL regeneration and formation of a pre‐osteoblast population. Intermediate phase (9–14 days): cell proliferation (shown by PCNA immunostaining)/migration led to osteoid/bone, PDL and cementum formation. Late phase (4–8 weeks): primarily characterized by tissue remodelling/maturation. Fibrous connective tissue from the gingival mucosa entered the wound early, competing with regeneration. By day 14, the wound space was largely filled with regenerative and reparative tissues. Conclusion Activation of cellular regenerative events in periodontal wound healing/regeneration is rapid; the general framework for tissue formation is broadly outlined within 14 days. Most bone formation apparently originates from endosteally derived pre‐osteoblasts; the PDL possibly acting as a supplementary source, with a primary function likely being regulatory/homeostatic. Blood accumulation at the surgical site warrants exploration; supplementation may be beneficial.
Bibliography:Georgia Health Sciences University College
istex:0468323AE0041334D72E056438FC4C192843A197
Georgia Health Sciences College of Dental Medicine
Figure S1. Critical aspects of the experimental surgery.Figure S2. IHC identification of clot fibers as fibrin.Figure S3. Representative photomicrographs from OAFH stained P3d specimens Day 2 and 5.Figure S4. Representative photomicrographs from OAFH stained P3d specimens Day 9 and 14.Figure S5. Representative photomicrographs from OAFH stained P3d specimens Week 4 and 8.Figure S6. Immunohistochemical identification of proliferating cells with PCNA.Figure S7. IHC identification of osteogenic cells. Figure S8. Negative controls for IHC staining.Figure S9. Fibroblast-like cells emerging above base of defect.Figure S10. Osterix expression in fibroblast-like presumptive cementoblast cells on root surface day 9.Appendix S1. Detailed materials and methods.
ark:/67375/WNG-LPLB3G1G-B
ArticleID:JCPE12055
US Army Advanced Education Program
Nobel Biocare
The authors declare no conflicts of interest.
Conflict of interest and source of funding statement
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0303-6979
1600-051X
DOI:10.1111/jcpe.12055