Published August 2011 | Version v1
Journal article

Phenotypic characterization of skeletal abnormalities of osteopotentia mutant mice by micro-CT: a descriptive approach with emphasis on reconstruction techniques

  • 1. Boston University Medical Center, Department of Radiology, Boston, MA (United States)
  • 2. University of California, San Francisco, Osteoporosis and Arthritis Research Group, San Francisco, CA (United States)
  • 3. Boston University School of Medicine, Quantitative Imaging Center, Boston, MA (United States)
  • 4. Department of Radiology, Klinikum Augsburg, Augsburg (Germany)
  • 5. Sligo General Hospital, Department of Radiology, Sligo (Ireland)
  • 6. University of Michigan Medical School, Osteoporosis and Arthritis Laboratory, Musculoskeletal Division, Department of Radiology, Ann Arbor, MI (United States)
  • 7. University of Erlangen, Department of Radiology, Erlangen (Germany)
  • 8. CCBR-SYNARC, Inc., San Francisco, CA (United States)
  • 9. University of California, Berkeley, Department of Molecular and Cell Biology and Center for Integrative Genomics, Berkeley, CA (United States)

Description

The novel protein osteopotentia (Opt) has recently been described as an essential regulator of postnatal osteoblast maturation and might possibly be responsible for some of the rarer types of osteogenesis imperfecta. Our aim was the evaluation of micro CT for the qualitative morphological assessment of skeletal abnormalities of Osteopotentia-mutant mice in comparison to radiography and histology. Four homozygous mice with insertional mutations in the Opt gene and three wild-type controls were examined ex vivo using radiography and micro-CT. Two of the homozygous animals were evaluated histologically (trichrome reagent). For the micro-CT evaluation three-dimensional (3D) surface reconstructions and two-dimensional (2D) multiplanar reformations (MPRs) were applied. The Opt-homozygous mice exhibited severe growth. The radiographic examinations showed osteopenia and fractures with hypertrophic callus formation and pseudarthroses of the forelimbs and ribs. Micro-CT confirmed these findings and was able to demonstrate additional fractures especially at smaller bones such as the metacarpals and phalanges. Additional characterization and superior delineation of cortices and fracture fragments was achieved by 2D MPRs. Histological correlation verified several of these imaging findings. Micro-CT is able to screen Opt-mutant mice for osseous pathologies and furthermore characterize these anomalies. The modality seems superior to conventional radiography, but is not able to demonstrate cellular pathology. However, histology is destructive and more time- and material-consuming than micro-CT. Additional information may be gathered by 2D MPRs. (orig.)

Availability note (English)

Available from: http://dx.doi.org/10.1007/s00256-010-1082-2

Additional details

Identifiers

Publishing Information

Journal Title
Skeletal Radiology
Journal Volume
40
Journal Issue
8
Journal Page Range
p. 1073-1078
ISSN
0364-2348
CODEN
SKRADI