[Suppressive effects for osteoclastogenesis regulated by RANKL signal].

Yoshiteru Miyauchi, Takeshi Miyamoto

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Abstract

RANKL signal promotes osteoclast differentiation through a transcriptional activation of responsible genes for osteoclast formation and functions. Recent works revealed that RANKL signal plays a role to repress transcription of suppressive factors for osteoclastogenesis. Some transcriptional repressors actively inhibit expressions of osteoclast-specific genes in the precursors through canceling the functions of transcription activators to prevent uncontrollable osteoclast formation and pathological bone resorption. The mouse models lacking those transcriptional repressors exhibited accelerated osteoclast differentiation and bone loss. Although the suppressive factors are important for maintaining bone homeostasis, they have to be removed for osteoclast formation in the presence of RANKL. The transcriptional repressor Blimp1 was identified as a new target of RANKL signal and strongly attenuated expressions of various suppressive factors including Bcl6. The osteoclast-specific Blimp1 knockout mice exhibited defect of osteclast formation and loss of bone resorption. Thus, RANKL signal regulates osteoclast differentiation by inducing transcriptional activators such as NFATc1 as well as transcriptional repressors such as Blimp1.The former is essential for expressions of osteclast-specific genes, while the latter is required for terminating suppressions of osteoclast differentiation.

Original languageEnglish
Pages (from-to)1141-1147
Number of pages7
JournalClinical calcium
Volume21
Issue number8
Publication statusPublished - 2011 Aug 1

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ASJC Scopus subject areas

  • Medicine(all)

Cite this

Miyauchi, Y., & Miyamoto, T. (2011). [Suppressive effects for osteoclastogenesis regulated by RANKL signal]. Clinical calcium, 21(8), 1141-1147.