Bone Marrow Transplantation Restores Follicular Maturation and Steroid Hormones Production in a Mouse Model for Primary Ovarian Failure
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Date
2012Author
Mohsen Ghadami
Ebtehal El-Demerdash
Dong Zhang
Salama A. Salama
Awadh A. Binhazim
Anthony E. Archibong
Xinlei Chen
Billy R. Ballard
M. Ram Sairam
Ayman Al-Hendy
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Recent studies suggest that bone marrow stem cells (BMSCs) are promising grafts to treat a variety of diseases, including
reproductive dysfunction. Primary ovarian failure is characterized by amenorrhea and infertility in a normal karyotype
female, with an elevated serum level of follicle-stimulating hormone (FSH) and a decrease level of estrogen caused by a
mutation in FSH receptor (FSHR) gene. Currently, there is no effective treatment for this condition. The phenotype of FSHR
(2/2) mouse, FORKO (follitropin receptor knockout), is a suitable model to study ovarian failure in humans. Female FORKO
mice have elevated FSH, decreased estrogen levels, are sterile because of the absence of folliculogenesis, and display thin
uteri and small nonfunctional ovaries. In this study, we determined the effects of BMSC transplantation on reproductive
physiology in this animal model. Twenty four hours post BMSC transplantation, treated animals showed detectable
estroidogeneic changes in daily vaginal smear. Significant increase in total body weight and reproductive organs was
observed in treated animals. Hemotoxylin and eosin (H&E) evaluation of the ovaries demonstrated significant increase in
both the maturation and the total number of the follicles in treated animals. The FSH dropped to 40–50% and estrogen
increased 4–5.5 times in the serum of treated animals compared to controls. The FSHR mRNA was detected in the ovaries of
treated animals. Our results show that intravenously injected BMSCs were able to reach the ovaries of FORKO mice,
differentiate and express FHSR gene, make FSHR responsive to FSH, resume estrogen hormone production, and restore
folliculogenesis.