Basically Scientific Research
Effect of mechano-growth factor on osteoclast activity and its mechanism
Tong Yanxiang, Wang Bin, Jia Yanfei, Feng Wei, Zhang Lifeng, Li Yaguang, Xue Fei, Yu Chengyong, Zhang Zhehan, Wang Wenxuan, Jia Wenchao, Wang Yi, Yang Youwei
Published 2021-11-15
Cite as Chin J Trauma, 2021, 37(11): 1034-1041. DOI: 10.3760/cma.j.cn501098-20210604-00328
Abstract
ObjectiveTo investigate the effect of mechano-growth factor(MGF)on osteoclast activity and its mechanism.
MethodsThe RAW264.7 precursor osteoclast cell line was cultured with 25 ng/ml macrophage-colony stimulating factor(M-CSF)and 30 ng/ml receptor activator of NF-κB ligand(RANKL),and identified by tartrate resistant acid phosphatase(TRAP)staining after 7 days of culture. Western blot anslysis was used to determine the effect of 45 ng/ml MGF on the phosphoinositide-3-kinase/protein kinase B(PI3K/AKT)signaling pathway in separated osteoclasts,including levels of AKT,phosphorylation(p)-AKT,lactation mammalian target of rapamycin(mTOR),p-mTOR and TRAP at 0,4,8 and 12 hours. Real-time fluorescence quantitative PCR was used to expressions of TRAP in osteoclasts at 0,4,8 and 12 hours. The PI3K/Akt phosphorylation inhibitor LY294002(20 μmol/L)combined with MGF(45 ng/ml)was used to act on osteoclasts,and expression levels of Akt,p-Akt,mTOR,p-mTOR and TRAP were detected by Western blot at 0,4,8 and 12 hours.
ResultsAfter culturing RAW264.7 cells with M-CSF and RANKL for 7 days,a large number of osteoclasts with positive TRAP staining can be obtained. Western blot analysis showed expression levels of Akt and mTOR did not change significantly over time(P>0.05),expression levels of p-Akt and p-mTOR increased continuously from(2.18±0.34)pg/ml and(0.83±0.10)pg/ml at 0 hour to(3.86±0.36)pg/ml and(1.56±0.19)pg/ml at 12 hours(P<0.05),and expression level of TRAP decreased significantly over time,from(5.66±0.47)pg/ml at 0 hour to(3.76±0.38)pg/ml at 12 hours(P<0.05). Real-time fluorescence quantitative PCR analysis of expression of TRAP in osteoclasts showed that MGF inhibited the expression of TRAP in osteoclasts,which decreased from 1.02±0.06 at 0 hour to 0.53±0.11 at 12 hours(P<0.05). After acting LY294002 combined with MGF on osteoclasts,Western blot analysis showed expression levels of Akt and mTOR did not change significantly over time(P>0.05),expression levels of p-AKT and p-mTOR decreased significantly from(3.28±0.18)pg/ml and(3.29±0.22)pg/ml at 0 hour to(2.06±0.34)pg/ml and(2.04±0.20)pg/ml at 12 hours(P<0.05),and expression level of TRAP had no significant difference over time(P>0.05).
ConclusionsMGF inhibits osteoclast activity by inhibiting the expression of TRAP in osteoclasts through PI3K/Akt signaling pathway. LY294002 inhibits the expression of PI3K/Akt signaling pathway in osteoclasts,further verifying the mechanism of MGF inhibiting osteoclast activity,and this finding puts forward new ideas for clinical prevention and treatment of osteoporosis.
Key words:
Osteoclasts; Phosphatidylinositol 3-kinase; Protein kinases; Mechano-growth factor
Contributor Information
Tong Yanxiang
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Wang Bin
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Inner Mongolia Medical University,Research Student Academy,Hohhot 010030,China
Jia Yanfei
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Feng Wei
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Zhang Lifeng
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Li Yaguang
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Xue Fei
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Yu Chengyong
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Zhang Zhehan
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Wang Wenxuan
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Jia Wenchao
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Wang Yi
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Yang Youwei
Department of Orthopedics,Second Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010030,China
Inner Mongolia Medical University,Research Student Academy,Hohhot 010030,China