AI Article Synopsis

  • Evidence shows that osteoporosis is linked to the dysfunction of bone mesenchymal stem cells (BMSCs), but many studies fall short in detailing the specific changes in these cells in osteoporosis.
  • In this research, BMSCs from ovariectomized and sham-operated rats were analyzed through RNA sequencing, revealing 14 mRNAs with significant regulation—7 up-regulated and 7 down-regulated—in osteoporotic BMSCs.
  • The findings indicate alterations in various biological processes associated with osteoporotic BMSCs, including cell viability and bone repair, and highlight potential RNA targets for future osteoporosis treatments.

Article Abstract

Evidence presented that osteoporosis is closely related to the dysfunction of bone mesenchymal stem cells (BMSCs). But most studies are insufficient to reveal what actually happens to the osteoporotic BMSCs. In this study, BMSCs were harvested from ovariectomized and sham-operated rats. After checking the characteristics of rat models and stem cells, the BMSCs were carried out for RNA sequencing. Part of the findings were verified that seven mRNAs (Abi3bp, Aifm3, Ccl11, Cdkn1c, Chst10, Id2, Vcam1) were significantly up-regulated in osteoporotic BMSCs while seven mRNAs (Cep63, Fgfr3, Myc, Omd, Pou2f1, Smarcal1, Timm10b) were down-regulated. In addition, potential miRNA-mRNA and lncRNA-mRNA regulatory networks were illustrated. The changes in osteoporotic BMSCs covered a large set of biological processes, including cell viability, differentiation, immunoreaction, bone repairment and estrogen defect. This study enriched the pathophysiological mechanisms of BMSCs and osteporosis, as well as provided dozens of attractive RNA targets for further treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10750345PMC
http://dx.doi.org/10.7150/ijms.88146DOI Listing

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