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MCP-5 suppresses osteoclast differentiation through Ccr5 upregulation.
Kim, Jung Ha; Kim, Kabsun; Kim, Inyoung; Seong, Semun; Koh, Jeong-Tae; Kim, Nacksung.
Affiliation
  • Kim JH; Department of Pharmacology, Chonnam National University Medical School, Gwangju, Republic of Korea.
  • Kim K; Hard-Tissue Biointerface Research Center, School of Dentistry, Chonnam National University, Gwangju, Republic of Korea.
  • Kim I; Department of Pharmacology, Chonnam National University Medical School, Gwangju, Republic of Korea.
  • Seong S; Department of Pharmacology, Chonnam National University Medical School, Gwangju, Republic of Korea.
  • Koh JT; Department of Pharmacology, Chonnam National University Medical School, Gwangju, Republic of Korea.
  • Kim N; Hard-Tissue Biointerface Research Center, School of Dentistry, Chonnam National University, Gwangju, Republic of Korea.
J Cell Physiol ; 239(2): e31171, 2024 Feb.
Article de En | MEDLINE | ID: mdl-38214098
ABSTRACT
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.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ostéoclastes / Glycoprotéines membranaires / Différenciation cellulaire / Protéines chimioattractives monocytaires Limites: Animals / Humans / Male Langue: En Journal: J Cell Physiol / J. cell. physiol / Journal of cellular physiology Année: 2024 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ostéoclastes / Glycoprotéines membranaires / Différenciation cellulaire / Protéines chimioattractives monocytaires Limites: Animals / Humans / Male Langue: En Journal: J Cell Physiol / J. cell. physiol / Journal of cellular physiology Année: 2024 Type de document: Article Pays de publication: États-Unis d'Amérique