Cation channel blocker-ruthenium red promoted osteoclastogenesis
Baoguo Mi, Hanfeng Guan, Wei Wu, Yong Li, Peng Tan, Feng Li
Abstract
Baoguo Mi, Hanfeng Guan, Wei Wu, Yong Li, Peng Tan, Feng Li
Abstract
Objective To investigate the effects of ruthenium red on the differentiation of osteoclasts and relative mechanism.Methods Receptor activator of nuclear factor-κB ligand (RANKL) was used to stimulate osteoclast differentiation.Osteoclast differentiation was assessed by tartrate-resistant acid phosphatase (TRAP) staining and the TRAP-positive cells were counted after exposure to 50 μg/L RANKL for 6 days.Tartrate-resistant acid phosphatase kit was used to evaluate TRAP activity.The expression of osteoclast specific genes [TRAP,Capthesin K (CK),matrix metalloproteinase (MMP)-9] mRNA expression was detected by using real-time quantitative reverse transcription-polymerase chain reaction (RT-qPCR).The receptor activator of nuclear factor κb(RANK) mRNA and protein expression was also detected.Resuits Ruthenium red promoted RANKL-stimulated osteoclast differentiation in Raw246.7 cell culture,as manifested by the increase of TRAP positive multinucleated cells and TRAP activity.In control group the TRAP A was 0.33 ± 0.04,and that in ruthenium red group was 0.43 ± 0.03.Ruthenium also up-regulated TRAP,CK,MMP-9 and RANK mRNA expression,and increased RANK protein expression.The difference between two groups was significant (P < 0.05).Conclusion Ruthenium red promoted osteoclast differentiation,which might by related to RANK-RANKL axis. Key words: Ruthenium red ; Osteoclastst; Differentiation
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Objective To investigate the effects of ruthenium red on the differentiation of osteoclasts and relative mechanism.Methods Receptor activator of nuclear factor-κB ligand (RANKL) was used to stimulate osteoclast differentiation.Osteoclast differentiation was assessed by tartrate-resistant acid phosphatase (TRAP) staining and the TRAP-positive cells were counted after exposure to 50 μg/L RANKL for 6 days.Tartrate-resistant acid phosphatase kit was used to evaluate TRAP activity.The expression of osteoclast specific genes [TRAP,Capthesin K (CK),matrix metalloproteinase (MMP)-9] mRNA expression was detected by using real-time quantitative reverse transcription-polymerase chain reaction (RT-qPCR).The receptor activator of nuclear factor κb(RANK) mRNA and protein expression was also detected.Resuits Ruthenium red promoted RANKL-stimulated osteoclast differentiation in Raw246.7 cell culture,as manifested by the increase of TRAP positive multinucleated cells and TRAP activity.In control group the TRAP A was 0.33 ± 0.04,and that in ruthenium red group was 0.43 ± 0.03.Ruthenium also up-regulated TRAP,CK,MMP-9 and RANK mRNA expression,and increased RANK protein expression.The difference between two groups was significant (P < 0.05).Conclusion Ruthenium red promoted osteoclast differentiation,which might by related to RANK-RANKL axis. Key words: Ruthenium red ; Osteoclastst; Differentiation
Key concepts: RANKL, Osteoclast, Acid phosphatase, Chemistry, Ruthenium red, Activator (genetics), Multinucleate, Ruthenium