Reactive oxygen species and oxidative stress in osteoclastogenesis, skeletal aging and bone diseases

No abstract is available for this paper.

• Publication year

  2015

• Venue

  Journal of Bone and Mineral Metabolism

• Publication date

  2015-03-26

• Fields of study

  Biology, Medicine, Chemistry, Environmental Science

• Identifiers
  DOI 10.1007/s00774-015-0656-4PMID 25804315
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Nrf2 deficiency induces oxidative stress and promotes RANKL-induced osteoclast differentiation.

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• Tea Polyphenols Inhibit Rat Osteoclast Formation and Differentiation.

  2012cited by this paper
• Tea polyphenols inhibit rat osteoclast formation and differentiation.

  2012cited by this paper
• Ormeloxifene inhibits osteoclast differentiation in parallel to downregulating RANKL-induced ROS generation and suppressing the activation of ERK and JNK in murine RAW264.7 cells.

  2012cited by this paper
• Antioxidants, like coenzyme Q10, selenite, and curcumin, inhibited osteoclast differentiation by suppressing reactive oxygen species generation.

  2012cited by this paper
• The E-loop Is Involved in Hydrogen Peroxide Formation by the NADPH Oxidase Nox4*

  2011cited by this paper
• Simvastatin inhibits osteoclast differentiation by scavenging reactive oxygen species

  2011cited by this paper
• Administration of zinc inhibits osteoclastogenesis through the suppression of RANK expression in bone.

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• Platinum nanoparticles suppress osteoclastogenesis through scavenging of reactive oxygen species produced in RAW264.7 cells.

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• NOX2 Complex–Derived ROS as Immune Regulators

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• Resveratrol prevents RANKL-induced osteoclast differentiation of murine osteoclast progenitor RAW 264.7 cells through inhibition of ROS production.

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• Ascorbic acid accelerates osteoclast formation and death.

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• Association of Oxidative Stress with Postmenopausal Osteoporosis and the Effects of Hydrogen Peroxide on Osteoclast Formation in Human Bone Marrow Cell Cultures

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• Role of mitochondrial reactive oxygen species in osteoclast differentiation

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• Continuous Treatment with a Low-Dose β-Agonist Reduces Bone Mass by Increasing Bone Resorption Without Suppressing Bone Formation

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• RANKL-mediated Reactive Oxygen Species Pathway That Induces Long Lasting Ca2+ Oscillations Essential for Osteoclastogenesis*

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• RANKL-mediated reactive oxygen species pathway that induces long lasting Ca2+ oscillations essential for osteoclastogenesis

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• Vitamin C intake inhibits serum lipid peroxidation and osteoclast differentiation on alveolar bone in rats fed on a high-cholesterol diet.

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• NADPH oxidase-derived reactive oxygen species are essential for differentiation of a mouse macrophage cell line (RAW264.7) into osteoclasts

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• NADPH oxidase-derived reactive oxygen species are essential for differentiation of a mouse macrophage cell line (RAW264.7) into osteoclasts.

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• Vitamin C intake inhibits serum lipid peroxidation and osteoclast differentiation on alveolar bone in rats fed on a high-cholesterol diet

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• Receptor activator of nuclear factor-kappaB ligand-induced mouse osteoclast differentiation is associated with switching between NADPH oxidase homologues.

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• Subcellular localization of Nox4 and regulation in diabetes

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• Simvastatin, 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase inhibitor, suppresses osteoclastogenesis induced by receptor activator of nuclear factor‐κB ligand through modulation of NF‐κB pathway

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• Rutin inhibits osteoclast formation by decreasing reactive oxygen species and TNF-alpha by inhibiting activation of NF-kappaB.

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• Baicalein inhibits osteoclast differentiation and induces mature osteoclast apoptosis.

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• Total oxidative/anti-oxidative status and relation to bone mineral density in osteoporosis

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• Dried Plum Polyphenols Inhibit Osteoclastogenesis by Downregulating NFATc1 and Inflammatory Mediators

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• Inhibition of osteoclast differentiation and bone resorption by sauchinone

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• Rutin inhibits osteoclast formation by decreasing reactive oxygen species and TNF-α by inhibiting activation of NF-κB

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• Inhibition of osteoclast differentiation and bone resorption by sauchinone.

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• Involvement of hydrogen peroxide in the differentiation and apoptosis of preosteoclastic cells exposed to arsenite.

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• Rac1 GTPase regulates osteoclast differentiation through TRANCE-induced NF-κB activation

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• Functional analysis of Nox4 reveals unique characteristics compared to other NADPH oxidases.

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• Antioxidant alpha-lipoic acid inhibits osteoclast differentiation by reducing nuclear factor-kappaB DNA binding and prevents in vivo bone resorption induced by receptor activator of nuclear factor-kappaB ligand and tumor necrosis factor-alpha.

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• Role of antioxidant systems, lipid peroxidation, and nitric oxide in postmenopausal osteoporosis

  2006cited by this paper
• Antioxidant α-lipoic acid inhibits osteoclast differentiation by reducing nuclear factor-κB DNA binding and prevents in vivo bone resorption induced by receptor activator of nuclear factor-κB ligand and tumor necrosis factor-α

  2006cited by this paper
• Dried plum prevents bone loss in a male osteoporosis model via IGF-I and the RANK pathway.

  2006cited by this paper
• Bimodal actions of reactive oxygen species in the differentiation and bone‐resorbing functions of osteoclasts

  2006cited by this paper
• Rac1 GTPase regulates osteoclast differentiation through TRANCE-induced NF-kappa B activation.

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• α-Lipoic acid suppresses osteoclastogenesis despite increasing the receptor activator of nuclear factor κB ligand/osteoprotegerin ratio in human bone marrow stromal cells

  2005cited by this paper
• A crucial role for reactive oxygen species in RANKL-induced osteoclast differentiation.

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• Alpha-lipoic acid suppresses osteoclastogenesis despite increasing the receptor activator of nuclear factor kappaB ligand/osteoprotegerin ratio in human bone marrow stromal cells.

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• Reactive Oxygen Species Stimulates Receptor Activator of NF-κB Ligand Expression in Osteoblast*

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• Hydrogen peroxide is essential for estrogen-deficiency bone loss and osteoclast formation.

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• The Journal of Experimental Medicine CORRESPONDENCE Hiroshi Takayanagi:

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• Lycopene I—Effect on Osteoclasts: Lycopene Inhibits Basal and Parathyroid Hormone-Stimulated Osteoclast Formation and Mineral Resorption Mediated by Reactive Oxygen Species in Rat Bone Marrow Cultures

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