Intramembranous Bone Healing Process Subsequent to Tooth Extraction in Mice: Micro-Computed Tomography, Histomorphometric and Molecular Characterization

Author(s)

Vieira, Andreia Espindola ^[1] ; Repeke, Carlos Eduardo ^[1] ; Ferreira Junior, Samuel de Barros ^[1] ; Colavite, Priscila Maria ^[1] ; Biguetti, Claudia Cristina ^[1] ; Oliveira, Rodrigo Cardoso ^[1] ; Assis, Gerson Francisco ^[1] ; Taga, Rumio ^[1] ; Favaro Trombone, Ana Paula ^[2] ; Garlet, Gustavo Pompermaier ^[1]

Affiliation

^[1] Univ Sao Paulo, Bauru Sch Dent, Dept Biol Sci, Bauru, SP - Brazil

^[2] Univ Sagrado Coracao, Dept Biol & Allied Hlth Sci, Bauru - Brazil

• Document type: Journal article
• Source: PLoS One; v. 10, n. 5 MAY 29 2015.
• Web of Science Citations: 32

Abstract

Bone tissue has a significant potential for healing, which involves a significant the interplay between bone and immune cells. While fracture healing represents a useful model to investigate endochondral bone healing, intramembranous bone healing models are yet to be developed and characterized. In this study, a micro-computed tomography, histomorphometric and molecular (RealTimePCRarray) characterization of post tooth-extraction alveolar bone healing was performed on C57Bl/6 WT mice. After the initial clot dominance (0h), the development of a provisional immature granulation tissue is evident (7d), characterized by marked cell proliferation, angiogenesis and inflammatory cells infiltration; associated with peaks of growth factors (BMP-2-4-7, TGF beta 1, VEGFa), cytokines (TNF alpha, IL-10), chemokines \& receptors (CXCL12, CCL25, CCR5, CXCR4), matrix (Col1a1-2, ITGA4, VTN, MMP1a) and MSCs (CD105, CD106, OCT4, NANOG, CD34, CD146) markers expression. Granulation tissue is sequentially replaced by more mature connective tissue (14d), characterized by inflammatory infiltrate reduction along the increased bone formation, marked expression of matrix remodeling enzymes (MMP-2-9), bone formation/maturation (RUNX2, ALP, DMP1, PHEX, SOST) markers, and chemokines \& receptors associated with healing (CCL2, CCL17, CCR2). No evidences of cartilage cells or tissue were observed, strengthening the intramembranous nature of bone healing. Bone microarchitecture analysis supports the evolving healing, with total tissue and bone volumes as trabecular number and thickness showing a progressive increase over time. The extraction socket healing process is considered complete (21d) when the dental socket is filled by trabeculae bone with well-defined medullary canals; it being the expression of mature bone markers prevalent at this period. Our data confirms the intramembranous bone healing nature of the model used, revealing parallels between the gene expression profile and the histomorphometric events and the potential participation of MCSs and immune cells in the healing process, supporting the forthcoming application of the model for the better understanding of the bone healing process. (AU)

• FAPESP's process: 09/11496-1 - Morphometric and molecular characterization of pro-and anti-inflammatory cytokines roles in the alveolar bone repair process under homeostatic and infectious conditions.
• Grantee: Andreia Espíndola Vieira
• Support Opportunities: Scholarships in Brazil - Doctorate
• FAPESP's process: 10/15755-9 - The role of pro- and anti-inflammatory cytokines in alveolar bone repair process under homeostatic and infectious conditions: histomorphometric and molecular characterization in a experimental murine model
• Grantee: Gustavo Pompermaier Garlet
• Support Opportunities: Regular Research Grants