Changes in Metabolism and Mitochondrial Bioenergetics during Polyethylene-Induced Osteoclastogenesis.
Nur Shukriyah Mohamad HazirNor Hamdan Mohamad YahayaMuhamad Syahrul Fitri ZawawiHanafi Ahmad DamanhuriNorazlina MohamedEkram AliasPublished in: International journal of molecular sciences (2022)
Changes in mitochondrial bioenergetics are believed to take place during osteoclastogenesis. This study aims to assess changes in mitochondrial bioenergetics and reactive oxygen species (ROS) levels during polyethylene (PE)-induced osteoclastogenesis in vitro. For this purpose, RAW264.7 cells were cultured for nine days and allowed to differentiate into osteoclasts in the presence of PE and RANKL. The total TRAP-positive cells, resorption activity, expression of osteoclast marker genes, ROS level, mitochondrial bioenergetics, glycolysis, and substrate utilization were measured. The effect of tocotrienols-rich fraction (TRF) treatment (50 ng/mL) on those parameters during PE-induced osteoclastogenesis was also studied. During PE-induced osteoclastogenesis, as depicted by an increase in TRAP-positive cells and gene expression of osteoclast-related markers, higher proton leak, higher extracellular acidification rate (ECAR), as well as higher levels of ROS and NADPH oxidases (NOXs) were observed in the differentiated cells. The oxidation level of some substrates in the differentiated group was higher than in other groups. TRF treatment significantly reduced the number of TRAP-positive osteoclasts, bone resorption activity, and ROS levels, as well as modulating the gene expression of antioxidant-related genes and mitochondrial function. In conclusion, changes in mitochondrial bioenergetics and substrate utilization were observed during PE-induced osteoclastogenesis, while TRF treatment modulated these changes.
Keyphrases
- bone loss
- reactive oxygen species
- oxidative stress
- induced apoptosis
- gene expression
- diabetic rats
- high glucose
- cell cycle arrest
- cell death
- dna damage
- drug induced
- dna methylation
- endothelial cells
- lps induced
- poor prognosis
- signaling pathway
- inflammatory response
- endoplasmic reticulum stress
- combination therapy
- nitric oxide
- pi k akt
- immune response
- soft tissue