Okafuji Norimasa, Liu Zi-Jun, King Gregory J
Department of Orthodontics, Matsumoto Dental University, Shiojiri, Japan.
Am J Orthod Dentofacial Orthop. 2006 Nov;130(5):612-21. doi: 10.1016/j.ajodo.2005.06.023.
The cellular mechanisms controlling distraction osteogenesis are not well understood. The purpose of this study was to examine the role of cell proliferation in the regulation of mandibular distraction osteogenesis.
Unilateral mandibular ramus osteotomies were performed on 125 3-month-old Sprague-Dawley rats. The rats were randomized into 4 distraction rate groups and distracted for 5 days after 3-day latency. Rats (7 or 8 from each rate group) were killed at 4 time points. The rats received 5-bromo-2-deoxyuridine (BrdU) injections (40 mg per kilogram, i.p.) at day 3 (end of latency).
Both intramembranous and endochondral ossification was seen in the osteogenesis area. BrdU+ mesenchymal progenitor cells were significantly higher at day 10 (P <.05) and were found most numerously around the sagittal middle portion of the gap (P <.01). The greatest numbers of BrdU+ osteocytes were seen at day 38 (P <.05). Both BrdU+ osteoclasts and chondrocytes peaked at day 24.
Mesenchymal progenitor cells are mostly recruited in the early consolidation period, but they decrease in the middle and late consolidation periods during mandibular distraction osteogenesis. The rapid rate might suppress or sustain the proliferation and differentiation of mesenchymal progenitor cells during mandibular distraction osteogenesis. BrdU+ cells can survive throughout the entire experimental period of 5 weeks.
控制牵张成骨的细胞机制尚未完全明确。本研究旨在探讨细胞增殖在调节下颌骨牵张成骨中的作用。
对125只3月龄的Sprague-Dawley大鼠进行单侧下颌升支截骨术。将大鼠随机分为4个牵张速率组,在3天延迟期后进行5天的牵张。在4个时间点处死大鼠(每个速率组7或8只)。大鼠在第3天(延迟期末)接受腹腔注射5-溴-2-脱氧尿苷(BrdU,40毫克/千克)。
在成骨区域可见膜内成骨和软骨内成骨。在第10天,BrdU+间充质祖细胞显著增多(P<.05),且在间隙矢状中部周围数量最多(P<.01)。在第38天可见数量最多的BrdU+骨细胞(P<.05)。BrdU+破骨细胞和软骨细胞均在第24天达到峰值。
在下颌骨牵张成骨过程中,间充质祖细胞主要在早期巩固期被募集,但在中期和后期巩固期数量减少。快速牵张速率可能在下颌骨牵张成骨过程中抑制或维持间充质祖细胞的增殖和分化。BrdU+细胞可在整个5周的实验期内存活。