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S100 Calcium-Binding Protein P Secreted from Megakaryocytes Promotes Osteoclast Maturation
Seung-Hoon Lee1,2,3, Hye Jung Ihn3, Eui Kyun Park4
1Department of Molecular Medicine, School of Medicine, Kyungpook National University, Daegu 41944, Korea.
Abstract:
Megakaryocytes (MKs) differentiate from hematopoietic stem cells and produce platelets at the final stage of differentiation. MKs directly interact with bone cells during bone remodeling. However, whether MKs are involved in regulating bone metabolism through indirect regulatory effects on bone cells is unclear. Here, we observed increased osteoclast differentiation of bone marrow-derived macrophages (BMMs) cultured in MK-cultured conditioned medium (MK CM), suggesting that this medium contains factors secreted from MKs that affect osteoclastogenesis. To identify the MK-secreted factor, DNA microarray analysis of the human leukemia cell line K562 and MKs was performed, and S100 calcium-binding protein P (S100P) was selected as a candidate gene affecting osteoclast differentiation. S100P was more highly expressed in MKs than in K562 cells, and showed higher levels in MK CM than in K562-cultured conditioned medium. In BMMs cultured in the presence of recombinant human S100P protein, osteoclast differentiation was promoted and marker gene expression was increased. The resorption area was significantly larger in S100P protein-treated osteoclasts, demonstrating enhanced resorption activity. Overall, S100P secreted from MKs promotes osteoclast differentiation and resorption activity, suggesting that MKs indirectly regulate osteoclast differentiation and activity through the paracrine action of S100P.
Insights
Megakaryocytes (MKs) secrete S100 calcium-binding protein P (S100P), which enhances osteoclast differentiation and activity. This finding suggests MKs indirectly regulate bone metabolism through S100P signaling.
Area of Science:
- Hematology
- Bone Biology
- Cell Signaling
Background:
- Megakaryocytes (MKs) are critical for platelet production and interact with bone cells during remodeling.
- The indirect regulatory role of MKs on bone metabolism via secreted factors remains largely unexplored.
Purpose of the Study:
- To investigate whether MKs influence osteoclast differentiation and activity.
- To identify MK-secreted factors involved in regulating osteoclastogenesis.
Main Methods:
- Culturing bone marrow-derived macrophages (BMMs) in MK-conditioned medium (MK CM).
- Utilizing DNA microarray analysis to identify candidate genes.
- Assessing osteoclast differentiation and resorption activity upon S100P protein treatment.
Main Results:
- MK CM promoted osteoclast differentiation.
- S100 calcium-binding protein P (S100P) was identified as a highly expressed MK-secreted factor.
- Recombinant S100P protein enhanced BMM osteoclast differentiation and osteoclast resorption activity.
Conclusions:
- MKs secrete S100P, which promotes osteoclast differentiation and resorption.
- MKs indirectly regulate osteoclast activity and bone metabolism through the paracrine action of S100P.
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