An in vitro model of radiation-induced craniofacial bone growth inhibition.

Radiation-induced craniofacial bone growth inhibition is a consequence of therapeutic radiation in the survivors of pediatric head and neck cancer. Previously, the infant rabbit orbitozygomatic complex (OZC) was established as a reliable animal model. The purpose of this study was to develop a cell culture model from the rabbit OZC to study the effects of radiation in the craniofacial skeleton. Infant (7-week-old) New Zealand white rabbits were used in this study. Periostea from both OZC were harvested in sterile conditions, introduced into cell culture by way of sequential digestion, and subcultured at confluence. Cultures were analyzed for cellular proliferation (methylthiazoletetrazolium assay), alkaline phosphatase activity, collagen type I expression, and mineralization. Electron microscopy was performed to reveal the in vitro ultrastructure. Subsequently, rabbits were irradiated with sham or 15 Gy radiation, and cell cultures were developed and analyzed for cell numbers. Cell cultures, grown from OZC periostea, expressed osteoblast-like phenotype, with high alkaline phosphatase activity, collagen type 1 expression, and mineralization in an osteogenic environment. Electron microscopy confirmed the characteristic ultrastructural features of osteogenesis in vitro. Finally, significantly (P < 0.01) fewer cells were obtained from animals treated with 15 Gy radiation compared with those from control animals.A primary cell culture with osteoblast-like cellular phenotype was developed from infant rabbit OZC periosteum. This cell culture system responded to in vivo administered radiation by a significant decrease in cell numbers. This in vitro model will be subsequently used to study the cellular mechanisms of radiation and radioprotection in craniofacial osteoblast-like cells.

The pneumatic spaces of the temporal bone: relationship to the temporomandibular joint.

OBJECTIVES: To assess the topographic relationship between the pneumatic spaces of the temporal bone and the temporomandibular joint (TMJ) using high-resolution CT. METHODS: Findings from 100 consecutive patients who had undergone high-resolution axial CT of the base of the skull were reviewed on a digital imaging workstation. Additional multiplanar reformatted images were created in the sagittal and coronal planes through the TMJ. The extension of the pneumatic spaces of the temporal bone and their relation to the TMJ were determined on both sides. RESULTS: The extent of pneumatisation of the temporal bone varied considerably. The roof of the TMJ fossa was pneumatised in 51 patients. The articular eminence contained air spaces in 12 patients, the root of the zygomatic process in five patients. Air cells in the peritubal area extended into the medial wall of the glenoid fossa 53 patients. In approximately 25% the extent of pneumatisation showed marked asymmetry. CONCLUSIONS: Pneumatisation of the temporal bone frequently extends close to the TMJ. Knowledge of these air spaces is helpful for the interpretation of imaging studies such as panoramic radiographs and to understand the spread of pathological processes into the joint.

The influence of bony architecture on fixed membranous bone graft survival.

The aim of this study was to examine the influence of membranous bone graft architecture on graft survival. Eighteen adult New Zealand rabbits underwent full-thickness harvesting of their zygoma, which was then divided into two parts, resulting in a wider, thicker anterior graft and a tapered posterior graft. The grafts were then rigidly fixed, one to each nasal bone, using titanium lag screws. On postgrafting days 15 and 45, 3 animals each were killed. The remaining 12 animals were killed on day 90. The graft, graft-host interface, and contralateral zygoma were assessed volumetrically, histologically (nondecalcified), and stereologically. Volumetrically, the anterior (thicker, wider) grafts demonstrated 100% survival while the posterior (thinner, more narrow) grafts demonstrated 80% survival (p = 0.004). Histologically, the anterior grafts demonstrated less resorption and porosity and greater labeling activity. At the graft-host interface, the anterior grafts exhibited a 2.5-fold increase in full incorporation of the grafts, and the posterior grafts had almost twice the incidence of nonincorporation. Stereological measurements, including interlabel width (20.3 microns anteriorly, 18.9 microns posteriorly), confirmed the enhanced survival of the anterior grafts. Using multiple forms of analyses, this study demonstrates that membranous bone graft architecture influences graft survival. To assist in understanding these differences, we also analyzed the normal contralateral zygoma. While the anterior and posterior halves had a relatively constant amount of bicortical bone, the thicker grafts had a proportionally greater trabecular component (i.e., increased diploë-to-cortical ratio). In the rabbit model, differences in membranous bone thickness imply differences in the cancellous portion of the graft, thereby influencing ultimate graft survival.

Multidimensional distraction osteogenesis: the canine zygoma.

The principle of distraction osteogenesis, well-established in the enchondral bones of the axial skeleton, has recently been applied to the membranous bones (mandible, cranium) of the craniofacial skeleton in the experimental animal and in the human. In the craniofacial skeleton, however, the technique has been used only to lengthen bone in a direction along its major axis, i.e., unidimensional distraction. A canine model is presented to demonstrate the feasibility of distracting membranous bone away from its dominant axis, i.e., multidimensional distraction. Four mongrel dogs, 5 months of age, were the subjects of this study. Two osteotomies were made in the zygomatic arch, and the bone-lengthening device was fixed to the zygoma. After 7 days of external fixation, the osteotomized segment was lengthened 1 mm/day away from the long axis of the bone for 15 days. External fixation was then maintained for a minimum of 4 weeks, after which the dogs were sacrificed. Craniofacial CT with three-dimensional reconstruction documented multidimensional bone lengthening, and histologic analysis of the specimen confirmed the presence of new cortical bone in the expanded areas. Refinement in technique and miniaturization and internalization of the bone-lengthening device may allow for more precise changes in the amount and direction of lengthening, thus making distraction osteogenesis more widely applicable for use in the human craniofacial skeleton.