Related Experiment Video
Updated: Jul 15, 2026

Evaluation of Stem Cell Properties in Human Ovarian Carcinoma Cells Using Multi and Single Cell-based Spheres Assays
Published on: January 3, 2015
Germline stem cells and neo-oogenesis in the adult human ovary
Yifei Liu1, Chao Wu, Qifeng Lyu
1College of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China.
Abstract:
It remains unclear whether neo-oogenesis occurs in postnatal ovaries of mammals, based on studies in mice. We thought to test whether adult human ovaries contain germline stem cells (GSCs) and undergo neo-oogenesis. Rather than using genetic manipulation which is unethical in humans, we took the approach of analyzing the expression of meiotic marker genes and genes for germ cell proliferation, which are required for neo-oogenesis, in adult human ovaries covering an age range from 28 to 53 years old, compared to testis and fetal ovaries served as positive controls. We show that active meiosis, neo-oogenesis and GSCs are unlikely to exist in normal, adult, human ovaries. No early meiotic-specific or oogenesis-associated mRNAs for SPO11, PRDM9, SCP1, TERT and NOBOX were detectable in adult human ovaries using RT-PCR, compared to fetal ovary and adult testis controls. These findings are further corroborated by the absence of early meiocytes and proliferating germ cells in adult human ovarian cortex probed with markers for meiosis (SCP3), oogonium (OCT3/4, c-KIT), and cell cycle progression (Ki-67, PCNA), in contrast to fetal ovary controls. If postnatal oogenesis is confirmed in mice, then this species would represent an exception to the rule that neo-oogenesis does not occur in adults.
Insights
Adult human ovaries do not appear to contain germline stem cells (GSCs) or undergo neo-oogenesis. Studies found no evidence of active meiosis or GSCs in women aged 28-53, contrasting with fetal ovaries.
Area of Science:
- Reproductive Biology
- Human Ovarian Physiology
- Developmental Biology
Background:
- The occurrence of neo-oogenesis (formation of new oocytes) in adult mammalian ovaries, particularly in humans, remains a subject of debate.
- Previous research, primarily in mice, has yielded conflicting results regarding the presence of germline stem cells (GSCs) and postnatal oogenesis.
Purpose of the Study:
- To investigate the potential for neo-oogenesis and the presence of GSCs in adult human ovaries.
- To analyze the expression of key genes associated with meiosis and germ cell proliferation in adult human ovarian tissue.
Main Methods:
- RT-PCR analysis of meiotic and oogenesis-associated genes (SPO11, PRDM9, SCP1, TERT, NOBOX) in adult human ovaries (28-53 years) and controls (fetal ovaries, adult testis).
- Immunohistochemical staining of adult human ovarian cortex using markers for meiosis (SCP3), oogonia (OCT3/4, c-KIT), and cell proliferation (Ki-67, PCNA).
Main Results:
- No detectable mRNAs for early meiotic or oogenesis-associated genes were found in adult human ovaries.
- Absence of early meiocytes and proliferating germ cells was confirmed in adult human ovarian cortex.
- Fetal ovaries and adult testes served as positive controls, showing expected gene expression and cell markers.
Conclusions:
- Active meiosis, neo-oogenesis, and the presence of GSCs are unlikely in normal adult human ovaries.
- The findings suggest that humans, unlike potentially mice, do not exhibit postnatal oogenesis.
- This study provides evidence against the existence of a self-renewing germline in adult human ovaries.
Related Concept Videos
Oogenesis
Oogenesis
Each primary oocyte is surrounded by a layer of pre-granulosa cells, forming what is known...
Folliculogenesis
Embryonic Stem Cells
ES cells are grown in a culture medium where they can divide indefinitely, creating ES cell lines. Under certain conditions, ES cells can differentiate, either spontaneously into a variety of...
Embryonic Stem Cells
Multipotency and Niche of Bulge Stem Cell

