Center for Systems Biomedical Science, University of Shanghai for Science and Technology
Yan ZHANG
Center for Systems Biomedical Science, University of Shanghai for Science and Technology
Xiao-li LI
Center for Systems Biomedical Science, University of Shanghai for Science and Technology
Shu-yan WU
Center for Systems Biomedical Science, University of Shanghai for Science and Technology
Teng-yue DIAO
Center for Systems Biomedical Science, University of Shanghai for Science and Technology
Rong HAI
Center for Systems Biomedical Science, University of Shanghai for Science and Technology
Hong-wen DENG
Center for Systems Biomedical Science, University of Shanghai for Science and Technology School of Public Health and Tropical Medicine, Tulane University
The local tissue-specific renin-angiotensin system (RAS) was identified. The aim of this study was to investigate the role of local bone RAS in the osteoporosis of aging mice. Twelve-month-old and two-month-old male mice were respectively assigned to the ageing and young groups. The tibias and femurs were collected for an analysis of histomorphology, bone mass, and gene and protein expression. H&E staining and micro-CT measurement showed a loss of the trabecular bone network and decrease of bone mineral density in the proximal tibial metaphysis of the aged mice. The PCR results indicated the significant up-regulation of renin and angiotensinogen (AGT) mRNA expression in both the tibia and femur of the ageing mice. Western blotting data showed that the tibial angiotensin II protein expression was significantly increased in the ageing group. The enhancement of renin and AGT expression in the bone tissue resulted in the increased production of angiotensin II which plays an important role in the pathology of age-related osteoporosis.
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