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BMC Cell Biol ; 14: 18, 2013 Mar 19.
Article in English | MEDLINE | ID: mdl-23510080

ABSTRACT

BACKGROUND: The objective of this study was to evaluate the effect of bone marrow mesenchymal stem cells (BMSCs) on the apoptosis of granulosa cells (GCs) in rats. RESULTS: Cisplatin increased GC apoptosis from 0.59% to 13.04% in the control and cisplatin treatment groups, respectively, which was significantly reduced upon co-culture with BMSCs to 4.84%. Cisplatin treatment increased p21 and bax and decreased c-myc mRNA expression, which was reversed upon co-culture with BMSCs. As compared to young rats, increased apoptosis was observed in the perimenopausal rats (P < 0.001). After 3 months, the apoptosis rate in the BMSC group was significantly lower than that of the control group (P = 0.007). CONCLUSIONS: BMSC therapy may protect against GC apoptosis induced by cisplatin and perimenopause. Further studies are necessary to evaluate therapeutic efficacy of BMSCs.


Subject(s)
Bone Marrow Cells/drug effects , Cisplatin/administration & dosage , Coculture Techniques/methods , Cyclin-Dependent Kinase Inhibitor p21/metabolism , Granulosa Cells/drug effects , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells/drug effects , Perimenopause/physiology , Animals , Apoptosis/drug effects , Bone Marrow Cells/physiology , Cells, Cultured , Cyclin-Dependent Kinase Inhibitor p21/genetics , Estrogens/administration & dosage , Female , Gene Expression Regulation/drug effects , Granulosa Cells/physiology , Mesenchymal Stem Cells/physiology , Proto-Oncogene Proteins c-myc/genetics , Proto-Oncogene Proteins c-myc/metabolism , Rats , Rats, Sprague-Dawley , bcl-2-Associated X Protein/genetics , bcl-2-Associated X Protein/metabolism
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