Molecular mechanism of nitric oxide-induced osteoblast apoptosis

Ruei-Ming Chen, Ta-Liang Chen, Wen-Ta Chiu, Chia Chen Chang

Research output: Contribution to journalArticle

62 Citations (Scopus)

Abstract

Nitric oxide (NO) can regulate osteoblast activities. Our previous study showed that NO induced osteoblast apoptosis [Chen RM, Liu HC, Lin YL, Jean WC, Chen JS, Wang JH. Nitric oxide induces osteoblast apoptosis through the de novo synthesis of Bax protein. J Orthop Res 2002;20:295-302]. This study was further aimed to evaluate the mechanism of NO-induced osteoblast apoptosis from the viewpoints of mitochondrial functions, intracellular oxidative stress, and the anti-apoptotic Bcl-2 protein using neonatal rat calvarial osteoblasts as the experimental model. Exposure of osteoblasts to sodium nitroprusside (SNP), an NO donor, significantly increased amounts of lactate dehydrogenase in the culture medium, and decreased cell viability in concentration- and time-dependent manners. Administration of SNP in osteoblasts time-dependently led to DNA fragmentation. The mitochondrial membrane potential was significantly reduced following SNP administration. SNP decreased complex I NADH dehydrogenase activity in a time-dependent manner. Levels of cellular adenosine triphosphate (ATP) were suppressed by SNP. In parallel with the mitochondrial dysfunction, SNP time-dependently increased levels of intracellular reactive oxygen species. Immunoblotting analysis revealed that SNP reduced Bcl-2 protein levels. Exposure to lipopolysaccharide (LPS) and IFN-γ significant increased endogenous nitrite production. In parallel with the increase in endogenous NO, administration of LPS and IFN-γ suppressed cell viability, mitochondrial membrane potential, and ATP synthesis. Results of this study show that NO released from SNP can induce osteoblast insults and apoptosis, and the mechanism may involve the modulation of mitochondrial functions, intracellular reactive oxygen species, and Bcl-2 protein.

Original languageEnglish
Pages (from-to)462-468
Number of pages7
JournalJournal of Orthopaedic Research
Volume23
Issue number2
DOIs
Publication statusPublished - Mar 2005

Fingerprint

Nitroprusside
Osteoblasts
Nitric Oxide
Apoptosis
Mitochondrial Membrane Potential
Lipopolysaccharides
Reactive Oxygen Species
Cell Survival
Adenosine Triphosphate
Electron Transport Complex I
bcl-2-Associated X Protein
Proteins
Nitric Oxide Donors
DNA Fragmentation
Nitrites
L-Lactate Dehydrogenase
Immunoblotting
NAD
Culture Media
Oxidative Stress

Keywords

  • Apoptosis
  • Bcl-2 protein
  • Mitochondrial functions
  • Nitric oxide
  • Osteoblasts
  • Reactive oxygen species

ASJC Scopus subject areas

  • Orthopedics and Sports Medicine

Cite this

Molecular mechanism of nitric oxide-induced osteoblast apoptosis. / Chen, Ruei-Ming; Chen, Ta-Liang; Chiu, Wen-Ta; Chang, Chia Chen.

In: Journal of Orthopaedic Research, Vol. 23, No. 2, 03.2005, p. 462-468.

Research output: Contribution to journalArticle

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