The discovery of a new type of bone cell may uncover therapeutic targets for a range of skeletal diseases.
The researchers say they look forward to exploring how the new type of bone cell may change the approach to osteoporosis and other skeletal diseases. Image: Shutterstock
Researchers at the Garvan Institute of Medical Research and UNSW Sydney have discovered a new type of bone cell that may reveal new therapeutic approaches for osteoporosis and other skeletal diseases.
The new cells, which the researchers term ‘osteomorphs’, are found in the blood and bone marrow, and fuse together to form osteoclasts, specialised cells that break down bone tissue. They have a unique genomic profile that reveals promising and as yet unexplored targets for therapy.
“This discovery is a game-changer, which not only helps us understand bone biology but presents significant new in-roads for osteoporosis therapy,” says co-senior author Professor Tri Phan, who heads the Intravital Microscopy and Gene Expression Lab at the Garvan Institute and is a Conjoint Professor at UNSW Medicine & Health. “Osteomorphs express several genes that seem to be linked to bone disease, which could lead scientists to entirely new ways to target osteoporosis.”
The discovery is published today in Cell.
A unique genetic signature
Using cutting-edge single cell RNA sequencing technology, which the researchers developed specifically for studying these cells in bone, the team found that the new cells switched on a number of genes.
“The profile of genes that were switched on in these cells was really interesting – while many genes were also expressed by osteoclasts, several were unique. This, together with the evidence of the new re-fusion processes observed by intravital imaging, convinced us that we had discovered a new cell type, which we called osteomorphs, after the Mighty Morphin Power Rangers,” says author, UNSW Conjoint Senior Lecturer Dr Weng Hua Khoo.
With colleagues at Imperial College London, the researchers deleted 40 of the genes switched on in osteomorphs in experimental models. They found that for 17 of these genes, the deletion impacted on the amount of bone and bone strength, indicating a critical role in controlling bone.
“When we further investigated human genomic data in publicly available databases, we found that genes switched on in osteomorphs were linked to human gene variants that lead to skeletal dysplasia and control bone mineral density,” says co-senior author UNSW Conjoint Professor Peter Croucher, Deputy Director of the Garvan Institute and head of the Bone Biology Lab.
“Together, these findings revealed just how crucial osteomorphs are in bone maintenance, and that understanding these cells and the genes that control them may reveal new therapeutic targets for skeletal disease.”
Explaining a common side effect
Beyond revealing new avenues for treatment, the team’s findings provide a possible explanation of a commonly observed clinical phenomenon.
“Some individuals who discontinue the osteoporosis treatment denosumab experience a reduction in bone mass and an increase in so-called ‘rebound vertebral fractures’,” explains Professor Phan.
The authors say that denosumab blocks a molecule that they found is needed for the osteomorphs to form osteoclasts. They suspect that patients who receive denosumab accumulate osteomorphs in their body, and that these are released to form osteoclasts, which resorb bone, when treatment is stopped.
The researchers say studying the effects of denosumab and other osteoporosis medication on osteomorphs may inform how those treatments could be improved and how their withdrawal effects could be prevented.
“While we don’t yet fully understand the role of osteomorphs, their existence has already led to a major step change in our understanding of the skeleton,” says Professor Croucher. “This research has been an enormous combined international effort across many scientific disciplines. We look forward to exploring how these cells may change the approach to osteoporosis and other skeletal diseases moving forward.”
Source – UNSW Sydney