Osteoporosis might be due to defects in mesenchymal stem cells (MSCs) that lead to reduced proliferation and osteoblast differentiation. We hypothesized that transplantation of MSCs into sites at risk for developing osteoporotic bone could improve bone structure and biomechanics. The aim of this study was to establish an osteoporosis rabbit model by ovariectomy (OVX), characterize the autologous MSCs from the OVX rabbits, and transplant the autologous MSCs into the OVX rabbits. MSCs harvested from bone marrow of normal and OVX rabbits were culture expanded and differentiated in osteogenic medium. Phenotypes were evaluated by collagen I immunostaining, von Kossa staining, and quantitative assays of bone-specific alkaline phosphatase (B-ALP) and osteocalcin (OCN). MSCs were transfected with green fluorescence protein (GFP) and implanted in the gluteus muscle to trace their fate in vivo. Cultured autologous MSCs from OVX rabbits were constructed in calcium alginate gels and then transplanted in the distal femurs. At 4 and 8 weeks after implantation, histomorphometrical and biomechanical analyses were performed on the samples. MSCs from OVX rabbits displayed higher B-ALP activity, but had similar OCN levels as compared to those from sham rabbits. After 8 weeks of implantation, more bone apposition was found in the MSC-alginate-treated group. Histomorphometry indicated increased trabecular thickness. Histology also illustrated improved microstructures with newly formed osteoids and enhanced trabecular thickness. In addition, biomechanical testing revealed stronger stiffness in the MSC-alginate treatment group. Therefore, this study implies that transplantation of MSCs can help to strengthen osteoporotic bone in rabbits.

Precision in femoral neck scans with dual energy X-ray absorptiometry (DXA) is affected by variability in positioning and subsequent repositioning of the femur for repeated scans. To study the in vitro effect of femoral rotation on the bone mineral density (BMD), four fresh-frozen cadaveric femurs were fixed in a specially designed jig which allows for rotation of the femurs. BMD measurements of the femurs were done in neutral position (0 degrees) i.e., with the femoral neck axis parallel to the surface of the couch and at 15 degrees, 30 degrees, and 45 degrees of internal and external rotation. In vivo precision of the femoral neck scan was determined in five normal male subjects. The scans were first done with the legs positioned using the manufacturer's foot block. Five scans were performed, with repositioning, on the left hip of each subject. The procedure was then repeated with the legs positioned using a custom-designed positioning jig to minimize the rotation of the hips during a scan. In the in vitro study, the femoral neck BMD value was minimum at neutral position (0 degrees) and increased when the femur was rotated internally or externally. In vivo precision error of the femoral neck scan was reduced by almost 50% with the use of the positioning jig when compared with the manufacturer's foot block. Femoral rotation was shown to have a significant effect on BMD measurements, and proper positioning of the femur during a scan can improve precision significantly.

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