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Published on: November 10, 2023
Myeloid-derived suppressor cells as a novel target for the control of osteolytic bone disease
Anandi Sawant1, Selvarangan Ponnazhagan
1Department of Pathology; University of Alabama at Birmingham; Birmingham, AL USA.
Abstract:
Myeloid-derived suppressor cells (MDSC) from mice bearing bone metastases differentiate into functional osteoclasts in vitro and in vivo, through a signaling pathway that relies on nitric oxide. In addition, MDSC-targeting drugs have been shown to robustly inhibit osteolysis. Thus, MDSC stand out as novel osteoclast progenitors and hence as candidate targets for the control of osteolytic bone disease.
Insights
Myeloid-derived suppressor cells (MDSC) are identified as new osteoclast progenitors. Targeting MDSC may offer a novel strategy to control bone diseases characterized by osteolysis.
Area of Science:
- Immunology
- Oncology
- Bone Biology
Background:
- Bone metastases are associated with significant osteolytic lesions.
- Osteoclasts are key cells responsible for bone resorption and osteolysis.
- The cellular origins of osteoclasts in the context of bone metastasis are not fully understood.
Purpose of the Study:
- To investigate the role of myeloid-derived suppressor cells (MDSC) in the development of osteoclasts.
- To explore the therapeutic potential of targeting MDSC for the control of osteolytic bone disease.
Main Methods:
- In vitro and in vivo differentiation assays of MDSC into osteoclasts.
- Analysis of the nitric oxide signaling pathway in MDSC differentiation.
- Evaluation of MDSC-targeting drugs in inhibiting osteolysis in mouse models.
Main Results:
- Myeloid-derived suppressor cells from mice with bone metastases differentiate into functional osteoclasts.
- This differentiation process is dependent on a nitric oxide signaling pathway.
- Drugs targeting MDSC demonstrated robust inhibition of osteolysis.
Conclusions:
- Myeloid-derived suppressor cells are identified as novel osteoclast progenitors.
- Targeting MDSC represents a promising therapeutic strategy for managing osteolytic bone diseases.
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