T63 inhibits osteoclast differentiation through regulating MAPKs and Akt signaling pathways

Xiao li Zhao, Jin jing Chen, Shu yi SI, Lin feng Chen, Zhen Wang

Research output: Contribution to journalArticlepeer-review


Inhibition of excessive osteoclast differentiation and activity is a valid approach for the treatment of osteoporosis. T63 is a small-molecule compound identified from a high throughput screening based on RUNX2 transcriptional activity, and has been reported to stimulate osteoblast formation. However, whether the compound has any effect on osteoclast differentiation remains unknown. Here, we examined the in vitro effect of T63 on osteoclastogenesis. T63 was found to inhibit the number of TRAP-positive cells in an osteoblast-osteoclast co-culture system, and inhibited Rankl expression in the preosteoblast MC3T3-E1 cells. The compound also directly suppressed RANKL-induced osteoclast differentiation in both dose- and time-dependent manner, as evidenced by the decrease of TRAP activity, F-actin formation and osteoclastogenesis-related genes expression in RAW264.7 cells. Moreover, pretreatment with T63 markedly decreased the activation of mitogen-activated protein kinases and Akt, both of which are positively involved in the regulation of osteoclastogenesis. Collectively, our findings suggest T63 has a protective effect against bone loss by inhibiting bone resorption. Its regulatory effect on bone metabolism makes the compound a more promising candidate for the potential application in the treatment of osteoporosis.

Original languageEnglish (US)
Pages (from-to)30-35
Number of pages6
JournalEuropean Journal of Pharmacology
StatePublished - Sep 5 2018


  • Osteoclastogenesis
  • Osteoporosis
  • T63

ASJC Scopus subject areas

  • Pharmacology


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