Defective bone repair in mast cell deficient mice with c-Kit loss of function
1 Bone Engineering Labs, Research Institute-McGill University Health Centre
2 Experimental Surgery
3 Experimental Medicine, Faculty of Medicine, McGill University
4 Biotechnology Program, University of British Columbia, 2329 West Mall, Vancouver, BC, Canada V6T 1Z4
5 Faculty of Medicine, University of Calgary, 2500 University Dr NW, Calgary, AB, Canada T2N 1N4
Abstract
KitW-sh mice carry an inactivating mutation in the gene encoding the receptor for stem cell factor, which is expressed at high levels on the surface of haematopoietic precursor cells. The mutation results in mast cell deficiency, a variety of defects in innate immunity and poorly defined abnormalities in bone. The present study was designed to characterise healing of a cortical window defect in skeletally mature KitW-sh mice using high-resolution micro computed tomographic imaging and histological analyses. The cortical bone defect healed completely in all wild type mice but failed to heal in about half of the KitW-sh mice by 12 weeks post-operative. Defective healing was associated with premature and excessive expression of TRAP positive cells embedded in fibrous marrow but with little change in ALP activity. Immuno-histochemical analyses revealed reduced CD34 positive vascular endothelial cells and F4/80 positive macrophages at 1 and 2 weeks post-operative. Impaired bone healing in the KitW-sh mice was therefore attributed to altered catabolic activity, impaired re-vascularisation and compromised replacement of woven with compact bone.
Keywords
- Osteo-immunology
- c-Kit and mast cell deficiency
- re-vascularisation
- bone regeneration
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