ABSTRACT
Stem cells are ideal seeding cells, which have the potential for self-renewal and multiple differentiation, and they play a fundamental role in maintaining homeostasis and regenerating and repairing tissue. The discovery of female germline stem cells (FGSCs) brings much hope for the postnatal renewal of oocytes and solving some female infertility problems. Ovarian function declines with increasing female age. Moreover, ovarian germline stem cell niche-aging could be the main cause of ovarian senescence, which ultimately leads to decreased follicle generation, declining female fertility, and age-related diseases, such as osteoporosis and ovarian cancer. The ovarian germline stem cell niche is the surrounding microenvironment in which FGSCs live, and it helps control the biological characteristics of FGSCs in many ways, such as nutritional supply and immunological cytokine secretion. This paper reviews the knowledge about the ovarian germline stem cell niche and its probable regulatory mechanisms on FGSCs, which provides valuable scientific information and scope for the prevention and treatment of ovarian senescence.
Abbreviations: BMP: bone morphogenetic protein; Dpp: decapentaplegic; FGSC: female germline stem cell; IL, interleukin; OGSC: ovarian germline stem cells; ROS: reactive oxygen species; TGF, transforming growth factor; TNF, tumor necrosis factor
Acknowledgments
The authors are thankful for the guidance of Professor YueHuiZheng and all of the authors’ help. Special thanks to Professor JuQiu from Institute of Health Sciences, Shanghai Academy of Life Sciences.
Disclosure statement
The authors have no conflicts of interest. The authors alone are responsible for the content and writing of this paper. All authors approved revisions and the final paper. Views expressed in the submitted article are our own and not an official position of the institution or funder.
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Yangchun Liu
Wrote the manuscript: YCL; Revising the manuscript: JX, FYZ, HFY, CH, JH, YHZ.