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...
Saved in:
Published in | Journal of clinical periodontology Vol. 40; no. 5; pp. 527 - 541 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.05.2013
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
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 |