Correlation Engine 2.0
Clear Search sequence regions


  • acid (1)
  • bone marrow (2)
  • Casp- 2 (10)
  • Casp2 (4)
  • cell fusion (1)
  • macrophages (3)
  • mice (3)
  • mice knockout (1)
  • NFATc1 (1)
  • osteoclasts (12)
  • oxygen (8)
  • protein levels (1)
  • SOD2 (1)
  • species (8)
  • Sizes of these terms reflect their relevance to your search.

    The loss of caspase-2 (Casp-2) in mice results in an osteopenic phenotype associated with increased numbers of osteoclasts in vivo. In this study, we show that Casp-2 is involved in osteoclastogenesis. Protein levels of Casp-2 decrease during the differentiation of macrophages to osteoclasts. Furthermore, siRNA-mediated Casp-2 knockdown in osteoclast precursors or differentiation of bone marrow macrophage (BMM) precursors from Casp2(-/-) mice results in increased osteoclast numbers and tartrate-resistant acid phosphatase (TRAP) activity. Casp2(-/-) osteoclasts are larger in size compared to wild-type osteoclasts and exhibited increased numbers of nuclei, perhaps due to increased precursor fusion. The loss of Casp-2 did not alter earlier stages of differentiation, but had a greater consequence on later stages involving NFATc1 auto-amplification and pre-osteoclast fusion. We have previously shown that the loss of Casp-2 results in increased oxidative stress in the bone. Reactive oxygen species (ROS) is known to play a critical role in late osteoclast differentiation and we show that total ROS and specifically, mitochondrial ROS, significantly increased in Casp2(-/-) BMM precursors after RANKL administration, with a concomitant reduction in FoxO3a and its target antioxidant enzymes, catalase and superoxide 2 (SOD2). Because mitochondrial ROS has been identified as a putative regulator of the later stages of differentiation, the heightened ROS levels in Casp2(-/-) cells likely promote precursor fusion and increased osteoclast numbers. In conclusion, our results indicate a novel role of Casp-2 in the osteoclast as a modulator of total and mitochondrial ROS and osteoclast differentiation. Copyright © 2015 Elsevier Inc. All rights reserved.

    Citation

    Danielle A Callaway, Manuel A Riquelme, Ramaswamy Sharma, Marisa Lopez-Cruzan, Brian A Herman, Jean X Jiang. Caspase-2 modulates osteoclastogenesis through down-regulating oxidative stress. Bone. 2015 Jul;76:40-8

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 25796569

    View Full Text