Immunolocalization of bone matrix macromolecules in human tissues regenerated from periodontal defects treated with expanded polytetrafluoroethylene membranes

• Published in: Archives of oral biology 1995-07, Vol.40 (7), p.653-661
• Main Authors: Amar, S., Petrungaro, P., Amar, A., Van Dyke, T.E.
• Format: Article
• Language: English
• Subjects: Adult; Alkaline Phosphatase - analysis; Alkaline Phosphatase - metabolism; Alveolar Process - physiology; bone macromolecules; Bone Matrix - chemistry; Bone Regeneration - physiology; Cells, Cultured; cementum; Culture Techniques; Dental Cementum - physiology; Dentistry; Extracellular Matrix Proteins - analysis; Extracellular Matrix Proteins - biosynthesis; Female; Guided Tissue Regeneration, Periodontal; Humans; Immunoenzyme Techniques; immunolocalization; Integrin-Binding Sialoprotein; Macromolecular Substances; Male; Membranes, Artificial; Middle Aged; Osteonectin - analysis; Osteonectin - biosynthesis; Periodontal Ligament - physiology; periodontal regeneration; Periodontium - chemistry; Periodontium - physiology; Polytetrafluoroethylene; Sialoglycoproteins - analysis; Sialoglycoproteins - biosynthesis; Space life sciences
• ISSN: 0003-9969; 1879-1506
• DOI: 10.1016/0003-9969(94)00201-L

Guided tissue regeneration (GTR) is a concept that evolved from the development of membrane barrier techniques which allow the repopulation of periodontal wounds by desirable cells, resulting in a so-called new attachment apparatus. To understand the biological mechanisms involved in membrane barrier-led periodontal healing, the histological localization of macromolecules phenotypical of bone and cementum formation was investigated in regenerating human periodontal tissues harvested after healing by placing barriers on teeth untreatable except by extraction. Using immunolocalization techniques, frozen sections of soft tissues and hard tissues under GTR barriers were stained with antibodies to osteonectin (LB-BON-II) and bone sialoprotein (BSP) (LF-6); alkaline phosphatase (AP) was detected histochemically. Frozen sections of regenerating periodontal tissue demonstrated the presence of spindle-shaped, fibroblast-like cells entrapped in a dense fibrillar extracellular matrix. Rounded cells aggregated to form nodules heavily stained by the Alcian blue method, indicating the presence of proteoglycans and strongly resembling those noted in hard-tissue sections. At the electron-microscopic level, the cytoplasm of the elongated cells had numerous cisternae of endoplasmic reticulum and Golgi saccules, indicating metabolic activity. Striated collagen fibres were scattered throughout the field of the sections. AP-stained soft-tissue sections demonstrated the presence cell-bound and extracellular AP. Osteonectin antibody staining confirmed the presence of this macromolecule in the extracellular matrix, particularly in the area of the cellular nodules. The dense network of connective tissue fibres was also stained. Both soft- and hard-tissue sections were stained with a human BSP antibody; an intense reaction was observed in demineralized hard-tissue sections in the area of bone-like tissue as well as in surrounding connective tissue organized into nodules. When the BSP distribution in hard-tissue sections was compared with that in soft-tissue sections, striking similarities of staining, particularly in the cellular nodules, were observed. The correlation between these histochemical findings strongly suggests that the forming soft tissues under GTR membrane contain cells and extracellular matrix macromolecules normally found in bone and cementum.