LIS1 Regulates Osteoclastogenesis through Modulation of M-SCF and RANKL Signaling Pathways and CDC42

Int J Biol Sci. 2016 Nov 25;12(12):1488-1499. doi: 10.7150/ijbs.15583. eCollection 2016.

Abstract

We have previously reported that depletion of LIS1, a key regulator of microtubules and cytoplasmic dynein motor complex, in osteoclast precursor cells by shRNAs attenuates osteoclastogenesis in vitro. However, the underlying mechanisms remain unclear. In this study, we show that conditional deletion of LIS1 in osteoclast progenitors in mice led to increased bone mass and decreased osteoclast number on trabecular bone. In vitro mechanistic studies revealed that loss of LIS1 had little effects on cell cycle progression but accelerated apoptosis of osteoclast precursor cells. Furthermore, deletion of LIS1 prevented prolonged activation of ERK by M-CSF and aberrantly enhanced prolonged JNK activation stimulated by RANKL. Finally, lack of LIS1 abrogated M-CSF and RANKL induced CDC42 activation and retroviral transduction of a constitutively active form of CDC42 partially rescued osteoclastogenesis in LIS1-deficient macrophages. Therefore, these data identify a key role of LIS1 in regulation of cell survival of osteoclast progenitors by modulating M-CSF and RANKL induced signaling pathways and CDC42 activation.

Keywords: Cdc42; LIS1; M-CSF; MAPK; RANKL; osteoclast..

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / genetics
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / metabolism*
  • Animals
  • Blotting, Western
  • Bone Marrow Cells / cytology
  • Cell Cycle / genetics
  • Cell Cycle / physiology
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cell Survival / genetics
  • Cell Survival / physiology
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Flow Cytometry
  • Male
  • Mice
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Monocytes / cytology
  • Monocytes / metabolism
  • Osteoclasts / cytology*
  • Osteoclasts / metabolism*
  • Osteogenesis / genetics
  • Osteogenesis / physiology*
  • RANK Ligand / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tartrate-Resistant Acid Phosphatase / metabolism
  • X-Ray Microtomography

Substances

  • Microtubule-Associated Proteins
  • RANK Ligand
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Pafah1b1 protein, mouse
  • Tartrate-Resistant Acid Phosphatase