AMP kinase acts as a negative regulator of RANKL in the differentiation of osteoclasts

  • Lee Y
  • Kim Y
  • Lee S
 et al. 
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Abstract

Introduction: AMP-activated protein kinase (AMPK) has been reported to stimulate differentiation and proliferation of osteoblasts, but the role of AMPK in the physiology of osteoclasts has not been investigated. Method: Osteoclasts were differentiated from mouse BMMφs. TRAP-positive multinucleated cells were considered to be osteoclasts using TRAP staining, and resorption area was determined by incubation of cells on dentine discs. Signaling pathways were investigated using Western blotting and RT-PCR. Results: RANKL induced phosphorylation/activation of AMPK-α in BMMφs and stimulated formation of TRAP-positive multinucleated cells. Pharmacological inhibition of AMPK with compound C and siRNA-mediated knockdown of AMPK-α1, the predominant α-subunit isoform in BMMφs, increased RANKL-induced formation of TRAP-positive multinucleated cells and bone resorption via activation of the downstream signaling elements p38, JNK, NF-κB, Akt, CREB, c-Fos, and NFATc1. STO-609, an inhibitor of CaMKK, completely blocked the RANKL-induced activation of AMPK-α, but KN-93, an inhibitor of CaMK, did not. siRNA-mediated TAK1 knockdown also blocked RANKL-induced activation of AMPK-α. The AMPK activators metformin, (-)-epigallocatechin-3-gallate, berberine, resveratrol, and α-lipoic acid dose-dependently suppressed formation of TRAP-positive multinucleated cells and bone resorption. Conclusion: AMPK negatively regulates RANKL, possibly by acting through CaMKK and TAK1. Thus, the development of AMPK activators may be a useful strategy for inhibiting the resorption of bone that is stimulated under RANKL-activated conditions. © 2010 Elsevier Inc.

Author-supplied keywords

  • AMP kinase
  • Bone resorption
  • Osteoclast
  • RANKL

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Authors

  • Young Sun Lee

  • Yang Soon Kim

  • Sun Young Lee

  • Geun Hyang Kim

  • Beom Jun Kim

  • Seung Hun Lee

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