Phenotypic characterization of skeletal abnormalities of osteopotentia mutant mice by micro-CT: a descriptive approach with emphasis on reconstruction techniques
Creators
- 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/s00256-010-1082-2Additional 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
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 43043938
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BIOMEDICAL RADIOGRAPHY; BONE FRACTURES; CARTILAGE; COMPUTERIZED TOMOGRAPHY; CONNECTIVE TISSUE CELLS; HISTOLOGY; HYBRIDIZATION; LIMBS; MALFORMATIONS; MICE; MUTANTS; PATHOGENESIS; PATHOLOGY; SKELETAL DISEASES; X-RAY RADIOGRAPHY
- Descriptors DEC
- ANIMAL CELLS; ANIMAL TISSUES; ANIMALS; BODY; CONNECTIVE TISSUE; DIAGNOSTIC TECHNIQUES; DISEASES; INDUSTRIAL RADIOGRAPHY; INJURIES; MAMMALS; MATERIALS TESTING; MEDICINE; NONDESTRUCTIVE TESTING; NUCLEAR MEDICINE; PATHOLOGICAL CHANGES; RADIOLOGY; RODENTS; SOMATIC CELLS; TESTING; TOMOGRAPHY; VERTEBRATES