Skip to content
logo The magazine for fitness, health and nutrition
Menopause Women's health All topics
Far from unnecessary!

What role the ovaries may play after menopause

Ovaries take on another important function after menopause
The ovaries appear to play an important role in women's health even after menopause. Photo: Getty Images
Share article

July 2, 2026, 5:57 pm | Read time: 5 minutes

As central female reproductive organs, the ovaries produce fertilizable eggs and generate the sex hormones estrogen and progesterone. However, with menopause, the supply of eggs is depleted, and the ovaries have long been considered largely inactive from this point on. All the more interesting are the results of a new study. According to this, the ovaries could possibly take on a new significant function after menopause: that of an immune organ.

Menopause refers to the time of a woman’s last natural menstrual period.1 With it, the fertile phase of life ends, as the supply of follicles (egg sacs in the ovaries) is now almost completely exhausted. Until now, little was known about what function the ovaries still fulfill from this moment on.

Also interesting: How women can recognize that their menopause has begun

Changed Role of the Ovaries After Menopause?

There were already indications that the ovaries are not entirely biologically inactive after menopause. These come from a study of 28 healthy women aged between 50 and 75, which a research team led by Francesca E. Duncan from Northwestern University has so far published as a preprint.2 The evaluation showed that a specific protein pattern of the ovaries continues to change even decades after menopause. In younger postmenopausal women, the researchers were able to detect increased proteins related to cell structure and gene regulation. In older participants, however, there were increasingly proteins involved in inflammatory processes, tissue remodeling, and innate immune defense. In addition, the researchers found indications that the ovaries in old age could increasingly release signaling proteins associated with general aging processes in the body.

A new study, which includes experiments with mice and in which researcher Duncan was also involved, builds on these observations.3

Details of the Study

The scientists examined the ovaries of female mice in three life stages:

  • at two months old, when the animals are fertile,
  • at 18 months (reproductive age), and
  • at 24 months in the post-reproductive phase.

One ovary from each animal was examined histologically (tissue examination), while the second was used for genetic analysis.

In the tissue samples, the researchers determined, among other things, the number of follicles. They also used special staining methods to make the collagen content in the tissue visible. Increased collagen deposition is considered a typical feature of fibrosis, an age-related hardening and structural remodeling of the tissue.

Additionally, the researchers used a method called bulk RNA sequencing. This method reveals which genes are particularly active in a tissue and allows conclusions about which biological processes are intensified or downregulated at different ages.

Finally, the team analyzed which immune cells are detectable in the ovary and examined genes whose products could presumably be released from the ovary to other body regions.

How the Ovaries Change

The number of follicles decreased significantly with age–this was expected. In the mice, the supply was almost exhausted by 18 months, and in the 24-month-old animals, no further significant decline was observed. At the same time, there was an increasing remodeling of the tissue, which the researchers attributed mainly to increased collagen deposition.

On a molecular level, the changes were particularly pronounced. When comparing young and post-reproductive mice, the researchers identified 8,515 differentially regulated genes. Many genes important for egg maturation, hormone production, and other reproductive processes showed significantly reduced activity. At the same time, the activity of genes associated with immune responses, inflammatory processes, and communication between immune cells increased.

More Immune Cells in the Tissue of Post-Reproductive Mice

The observed genetic changes were also reflected in the tissue. The research team found significantly more T-cells, macrophages, and multinucleated giant cells in the ovaries of older animals–all of which are part of the immune system. Additionally, the ovaries of the 24-month-old mice continued to differ from those of the 18-month-old animals. The researchers interpreted this as indicating that molecular remodeling processes occur even after the end of reproductive capability.

Furthermore, the researchers identified numerous genes whose products could presumably be secreted by the ovary. Many of these are associated with inflammatory reactions or immunological processes. A possible explanation for this could be that the post-reproductive ovary sends signals to other organs.

More on the topic

Possible Significance of the Results

The ovaries are apparently not biologically inactive after the end of their reproductive function–that is, after menopause. At least in the mouse model, they instead develop properties that could be associated with immune processes and the defense against pathogens.

Whether new therapies can be derived from this in the future is still completely open. However, the study authors hope that the observed changes can also be confirmed in humans. This could help to better understand the biological changes in the female body after menopause.

The researchers suspect that inflammation-promoting signaling substances from the ovaries could influence age-related changes in other organs. But more than a suspicion, it is not yet, as the possible connection was not part of the present study. However, it would at least be conceivable to specifically influence the inflammatory processes in the ovary without disturbing the hormonal balance.

Limitations

Even though mice are generally well-suited as a model for studying reproductive aging, they naturally differ from humans in several respects. Therefore, the results cannot be directly transferred to women.

It should also be noted that the applied RNA sequencing only captures the activity of genes. What effects this has on the entire body is still speculative. Additionally, the researchers cannot say with certainty whether more immune cells actually migrate into the ovary or whether the ovarian cells increasingly develop immune-like properties.

Thus, further studies are necessary, especially on human tissue, the researchers emphasize. Only then can the significance of the observed changes for the health of women after menopause be reliably assessed.

This article is a machine translation of the original German version of FITBOOK and has been reviewed for accuracy and quality by a native speaker. For feedback, please contact us at info@fitbook.de.

Sources

You have successfully withdrawn your consent to the processing of personal data through tracking and advertising when using this website. You can now consent to data processing again or object to legitimate interests.