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Oocyte generation in adult mammalian ovaries by putative germ cells in bone marrow and peripheral blood.


genetics, Tumor Suppressor Proteins, Sterilization, Reproductive, Protein-Serine-Threonine Kinases, Peripheral Blood Stem Cell Transplantation, cytology, Ovary, Oogenesis, Oocytes, Mice, Transgenic, Mice, Mutant Strains, Mice, Humans, Female, DNA-Binding Proteins, Cell Cycle Proteins, Bone Marrow Transplantation, Bone Marrow Cells, metabolism, Bone Marrow, Biological Markers, Ataxia Telangiectasia Mutated Proteins, Animals, Adult

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      It has been suggested that germline stem cells maintain oogenesis in postnatal mouse ovaries. Here we show that adult mouse ovaries rapidly generate hundreds of oocytes, despite a small premeiotic germ cell pool. In considering the possibility of an extragonadal source of germ cells, we show expression of germline markers in bone marrow (BM). Further, BM transplantation restores oocyte production in wild-type mice sterilized by chemotherapy, as well as in ataxia telangiectasia-mutated gene-deficient mice, which are otherwise incapable of making oocytes. Donor-derived oocytes are also observed in female mice following peripheral blood transplantation. Although the fertilizability and developmental competency of the BM and peripheral blood-derived oocytes remain to be established, their morphology, enclosure within follicles, and expression of germ-cell- and oocyte-specific markers collectively support that these cells are bona fide oocytes. These results identify BM as a potential source of germ cells that could sustain oocyte production in adulthood.

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