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Study 29 of 29MOTS-C literatureReproduction & fertility · Observational2026

The Mitochondrial-Derived Peptide MOTS-c Improves Bioenergetics in Aging-Associated Granulosa Cells and Oocytes.

MOTS-c improved energy production and cell structure in aging granulosa cells and oocytes, but did not fully restore egg maturation to levels seen in young mice.

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Where it sits

this study against the rest of the mots-c corpus
12
Preclinical
14
Observational · this one
0
Open-label
1
Randomised
2
Reviews

Summary and findings

This study investigated the effects of MOTS-c on aging-associated granulosa cells and oocytes. Laboratory experiments were conducted using aged human granulosa cells and eggs from aged mice. The findings indicated that MOTS-c improved energy production and cell structure, but did not restore egg maturation to levels seen in young mice.

How much of this paper we could read: full text read (0.70). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Not reported in abstract.2026

Abstract

The authors’ words, as Reproduction & fertility supplied them

<h4>Lay summary</h4>As women age, the quality of their eggs declines, which is a major contributor to age-related infertility. Eggs are supported by neighboring "helper" cells called granulosa cells, which act like a support crew that supplies the egg with the energy it needs to mature. These helper cells contain mitochondria, tiny energy-generating structures often called the cell's "powerhouses," and with age these powerhouses become less efficient, leaving eggs with less support than they need. This study tested whether MOTS-c, a small molecule naturally produced by mitochondria, could restore the function of these aging helper cells. In laboratory experiments using aged human granulosa cells and eggs from aged mice, MOTS-c boosted energy production and helped maintain cell structure, and was associated with improved egg maturation compared with untreated aged eggs, although treated eggs did not fully reach the maturation levels seen in young mice. These findings are from laboratory and animal experiments, not from women, and this study did not test whether MOTS-c affects fertilization, embryo development, or live birth. Further research is needed before any conclusions can be drawn about its relevance to human fertility.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Limitations

Not reported in abstract.

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