How load stimulates bone formation via the expression of osteocrin
When things get too much, we’re often advised to ‘take a load off’, but when it comes to bone maintenance, doing the opposite can be a good thing. Researchers from Japan have discovered some key mechanisms of how physical load stimulates bone growth.
In a study published on July 13 in Cell Reports, researchers from the National Cerebral and Cardiovascular Center Research Institute have revealed that the expression of the peptide osteocrin (OSTN) is influenced by load—decreasing when load is reduced, and increasing when it is added.
Bones and skeletal muscles are strengthened by the load associated with exercise, preventing bone and muscle atrophy, and maintaining bone and muscle strength is important for maintaining physical activity. The growth of long bones, such as the femur and tibia, is a very complex process controlled by genetic and environmental factors, such as exercise and gravity.
“Not much is known about how mechanical force initiates biochemical signals to control bone growth,” says lead author of the study Haruko Watanabe-Takano. “We investigated how load is related to the metabolic balance adjustment of bone maintenance.”
Bone is maintained by the balanced activities of two types of cells—osteoblasts, which make bone, and osteoclasts, which break down bone—and is thought to be made in response to load demand. Specifically, the team investigated the expression of OSTN, a peptide produced by osteoblasts, in mice. OSTN is critical to the regulation of bone growth, as well as physical endurance.
The researchers found that OSTN was very strongly expressed in bones such as the tibia, radius, and ulna, and in the region where the load was applied. Additionally, they showed that OSTN was secreted by the periosteal osteoblasts in these bones. The periosteum is a membrane found on the outer surface of bones, except at the joints of long bones, and is involved in bone remodeling and production, especially during growth.
“We also found that OSTN expression decreased when load was reduced, and was increased by load stimulation,” says Watanabe-Takano. “Moreover, when we genetically engineered mice lacking OSTN, we found that they had reduced bone mass compared with normal mice and lacked load-induced recovery of bone mass after prolonged load reduction. Thus, we concluded that OSTN makes bone in response to stimulation by load, promoting bone formation.”
When they looked into how OSTN might achieve this effect, the team found that it increases levels of another peptide, called C natriuretic peptide, which in turn drives bone-forming osteoblasts to multiply, mature, and become functional.
The results of this study will be useful for the promotion of bone maintenance in bedridden patients, because bone formation is known to be inhibited by long-term bed rest, and for the prevention and treatment of frailty syndrome. Future studies will build on these results to discover further mechanisms, such as how periosteal cells detect load stimulation.