0259 Apoptosis of Osteoprogenitor Cells in the Rat Extraction Socket
H. DEVLIN, Temple University School of Dentistry, Philadelphia, PA, USA, Y.D. HSIEH, The Military Kao Hsiung General Hospital, Kaoshiung, Taiwan, and J. HOYLAND, University of Manchester

Objective: The objective of the investigation was to observe the degree of apoptosis in the osteoblast, pre-osteoblast and osteoprogenitor populations in the rat tooth socket at various intervals after extraction.

Methods: With ethical committee approval, the upper right maxillary first molar of 7 mature rats was removed under general anesthesia. The rats were given a soft diet and killed at days 3, 5, 7, 10, 14, 21, and 28 after extraction. The cranio-maxillary tissues were processed for wax embedding. 5µm thick sections were prepared and stained using the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick-end-labeling method (TUNEL).

Results: Maximum staining in the socket and periosteal region of the facial alveolar bone occurred at 5, 7 and 10 days after extraction, which corresponds to the onset of woven bone formation. During this time interval, TUNEL-positive staining was seen in the osteoprogenitor and pre-osteoblast populations and especially strongly in the osteocytes of the woven bone. Staining was generally absent from osteoblasts, contradicting previous in-vitro studies. At the later time points, days 21 and 28 after extraction, TUNEL-staining was present only in some marrow cells and outer layers of the periosteum.

Conclusions: Cell death was most evident in the osteoprogenitor cells during active bone formation in the extraction socket and in osteocytes in the woven bone prior to secondary remodeling

Seq #42 - Landmark Studies and Arthur R. Frechette Research Award Finalists
9:00 AM-11:00 AM, Thursday, 26 June 2003 Svenska Massan A5

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