Trabecular bone turnover, bone marrow cell development, and gene expression of bone matrix proteins after low calcium feeding in rats
Low-calcium-fed animals have been accepted as one of the experimental models showing a
reduction in bone mass. However, the effects of short-term low-calcium feeding on bone
turnover, the development of osteoprogenitor cells, and gene expression of bone matrix
proteins have not been reported. In this study, we examined the effect of a low-calcium diet
on rat tibia and analyzed the changes in the bone by histomorphometry, bone marrow cell
culture, and in situ and Northern hybridization of the bone matrix proteins. Rats were fed …
reduction in bone mass. However, the effects of short-term low-calcium feeding on bone
turnover, the development of osteoprogenitor cells, and gene expression of bone matrix
proteins have not been reported. In this study, we examined the effect of a low-calcium diet
on rat tibia and analyzed the changes in the bone by histomorphometry, bone marrow cell
culture, and in situ and Northern hybridization of the bone matrix proteins. Rats were fed …
Low-calcium-fed animals have been accepted as one of the experimental models showing a reduction in bone mass. However, the effects of short-term low-calcium feeding on bone turnover, the development of osteoprogenitor cells, and gene expression of bone matrix proteins have not been reported. In this study, we examined the effect of a low-calcium diet on rat tibia and analyzed the changes in the bone by histomorphometry, bone marrow cell culture, and in situ and Northern hybridization of the bone matrix proteins. Rats were fed either a low-calcium diet (0.05% Ca) or a normal calcium diet (0.5% Ca) using the pair feeding technique. They were killed at day 0, 12 h, and days 1, 2, and 3. In the low-calcium group, the serum parathyroid hormone (PTH) level was temporarily increased in 12 h after feeding the low-calcium diet. Bone mineral density in the trabecular bone was significantly decreased from 1 day after the low-calcium feeding, but cortical bone did not show any changes during the experimental period. The bone volume per tissue volume in the proximal tibia also decreased from day 1 in the low-calcium group. The number of osteoclasts and osteoblasts on the trabecular bone surface was increased in the low-calcium group compared with the normal-calcium group. An ex vivo study showed that the number of progenitors of osteoclasts and osteoblasts in bone marrow was also increased in the low-calcium group of rats. The localization of type I collagen mRNA was observed in osteoblasts in the low-calcium group. The Northern hybridization study showed that the gene expression of type I collagen, osteopontin, and osteocalcin was increased at day 3 in the low-calcium group. These results indicated that the trabecular bone surface quickly responded to the low-calcium feeding and that bone remodeling activity was activated probably by PTH. The changes in bone marrow cell populations and the gene expression of bone matrix proteins are closely associated with increased bone turnover induced by the low-calcium diet, resulting in rapid bone loss of the trabecular bone.
Elsevier