4.3 Article

BMP4 localization and PCNA expression during distraction osteogenesis of the porcine mandible

Journal

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.ijom.2011.12.032

Keywords

mandibular distraction osteogenesis; immunohistochemistry; PCNA; BMP4

Funding

  1. AO-ASIF Foundation (Berne, Switzerland)
  2. Hanson Foundation (Boston, MA)
  3. CMF (West Chester, PA)
  4. Massachusetts General Hospital Oral and Maxillofacial Surgery Education and Research Fund (Boston, MA)
  5. Harvard Medical School Office of Enrichment

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This study characterized sequential molecular and cellular events in the porcine mandibular distraction osteogenesis (DO) wound. Nineteen Yucatan minipigs were divided into three treatment groups: Group A, unilateral mandibular distraction with 0 day latency, 1 mm/day rate for 12 days, 24 days fixation (n = 16); Group B, acute lengthening 12 mm (n = 2); Group C, sham control (n = 1). Group A was further divided by death date: mid-DO (n = 5), end-DO (n = 4), mid-fixation (n = 5) and end-fixation (n = 2). Groups B and C were killed on postoperative day 36, corresponding to end-fixation. Specimens were stained for proliferating cell nuclear antigen (PCNA) and bone morphogenetic protein-4 (BMP4). Cellular proliferation (PCNA) was assessed quantitatively and BMP4 staining was assessed on a semi-quantitative scale. Progenitor cell proliferation was greatest during mid-DO and decreased from end-DO through end-fixation. Proliferation in the acute lengthening group was elevated relative to sham control and comparable to end-DO. BMP4 staining intensity (localized to the periosteal cambium layer) was greatest during mid- and end-DO, decreased at mid-fixation and was undetectable at end-fixation. Progenitor cell proliferation and BMP4 expression are greatest during mid-DO and decrease progressively thereafter. At the time of death of the acute lengthening group, only increased cell proliferation was demonstrated.

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