A research team from the National University of Singapore (NUS) has identified a new avenue to maintain bone health while reducing bone resorption. The work, led by Associate Professor Christoph Winkler from the Department of Biological Sciences at the NUS Faculty of Science, opens up new and potentially more effective osteoporosis treatments.
Osteoporosis is the most common age-related bone disease worldwide. It is estimated that one in three women and one in five men aged over 50 suffer from osteoporotic bone fractures. In aging populations, the incidence of hip fractures increases dramatically, resulting in a high risk of morbidity and mortality. As such, osteoporosis is an immediate and significant health concern in Singapore and worldwide.
To develop new strategies to treat osteoporosis, the NUS team, which also comprised Dr. Phan Quang Tien and Dr. Tan Wen Hui from the NUS Department of Biological Sciences, collaborated with research groups from the Genome Institute Singapore and the University of Wuerzburg. They used genetic analysis to discover a connection between a small protein, chemokine CXCL9, and a vital part in maintaining healthy bones. They also identified two inhibitors as promising drug targets for osteoporosis.
This pioneering work was published in the journal Proceedings of the National Academy of Sciences (PNAS) on 27 July 2020.
The role of a small protein in osteoporosis
Osteoporosis is caused by excessive activity of bone-resorbing cells, called ‘osteoclasts,’ and reduced activity of bone-forming cells, called ‘osteoblasts.’ In healthy individuals, the balanced activity of these two cell types allows constant bone turnover to maintain healthy bones. However, with osteoporosis, disproportionate bone resorption leads to low bone mineral density and weak and fracture-prone bones.
The NUS team showed that the small protein, chemokine CXCL9, plays a role in osteoporosis when it is released from osteoblasts located on the surface of the bone matrix. Under osteoporotic conditions, CXCL9 diffuses towards reservoirs that hold osteoclast precursors. These osteoclast precursors produce a receptor, CXCR3, on their cell surface. Upon activation by CXCL9, the osteoclast precursors are mobilized and migrate long distances in a highly directed fashion towards the bone matrix, where they start resorbing bone.
Both CXCL9 and its receptor CXCR3 have long been known to modulate the migration of immune cells to inflammation sites, such as psoriasis and rheumatoid arthritis. Their role in osteoporosis and recruitment of bone cells, however, is unknown. The small-molecule inhibitors AMG-487 and NBI-74330 were known to block CXCR3 activity but have had little success in earlier clinical tests to treat psoriasis. The research team now showed that these inhibitors effectively prevent osteoclast recruitment and protect bone from osteoporotic effects.
New avenues to osteoporosis therapy
Most current osteoporosis therapies include the use of bisphosphonates, which block osteoclast activity and thus prevent excessive bone resorption. However, prolonged treatment with these drugs eliminates the necessary bone turnover leading to increased fracture risk and other unwanted side effects. Therefore, there is an urgent need to develop new strategies that overcome the limitations of current treatments.
“Based on our studies, both AMG-487 and NBI-74330 lowered the number of formed osteoclasts by more than 50 percent when administered at the efficient dosage. While these two inhibitors have been tested in preclinical and clinical trials, they have not been used as osteoporosis targets. We propose that the two small-molecule antagonists can be used to modulate or adjust excessive osteoclast numbers in osteoporosis patients in a dose-dependent fashion,” said Assoc Prof Winkler.
He added, “Our new strategy has major advantages as excessive bone resorption can be prevented in a targeted manner, but normal bone turnover will continue. This offers the potential to avoid increased fracture risks in osteoporosis patients and maintain healthy bone for improved quality of life.”
- Quang Tien Phan et al. Cxcl9l and Cxcr3.2 regulate the recruitment of osteoclast progenitors to bone matrix in a medaka osteoporosis model. DOI: 10.1073/pnas.2006093117