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MCP-5 suppresses osteoclast differentiation through Ccr5 upregulation.

Jung Ha KimKabsun KimInyoung KimSemun SeongJeong Tae KohNack-Sung Kim
Published in: Journal of cellular physiology (2024)
Human monocyte chemoattractant protein-1 (MCP-1) in mice has two orthologs, MCP-1 and MCP-5. MCP-1, which is highly expressed in osteoclasts rather than in osteoclast precursor cells, is an important factor in osteoclast differentiation. However, the roles of MCP-5 in osteoclasts are completely unknown. In this study, contrary to MCP-1, MCP-5 was downregulated during receptor activator of nuclear factor kappa B ligand (RANKL)-induced osteoclast differentiation and was considered an inhibitory factor in osteoclast differentiation. The inhibitory role of MCP-5 in osteoclast differentiation was closely related to the increase in Ccr5 expression and the inhibition of IκB degradation by RANKL. Transgenic mice expressing MCP-5 controlled by Mx-1 promoter exhibited an increased bone mass because of a decrease in osteoclasts. This result strongly supported that MCP-5 negatively regulated osteoclast differentiation. MCP-5 also prevented severe bone loss caused by RANKL.
Keyphrases
  • bone loss
  • nuclear factor
  • toll like receptor
  • dendritic cells
  • endothelial cells
  • poor prognosis
  • transcription factor
  • type diabetes
  • cell proliferation
  • adipose tissue
  • metabolic syndrome
  • high glucose
  • drug induced