Study record

Mitochondrial-encoded peptide MOTS-c prevents pancreatic islet cell senescence to delay diabetes

Kong BS, Lee H, L'Yi S et al. · Exp Mol Med · 2025

AnimalSeveralEvidence tier CAlso: Tissue / sample study (ex vivo)Also: Human observational

What this study reported

Reported that MOTS-c levels decreased with aging and senescence in pancreatic islet cells in mice. Found that treating isolated aged C57BL/6 mouse islets with MOTS-c reduced islet senescence alongside changes in nuclear gene expression and senescence-related metabolites, and that MOTS-c treatment reduced islet senescence and glucose intolerance in S961-treated C57BL/6 mice and in nonobese diabetic mice. Measured circulating MOTS-c in people and found lower levels in those with type 2 diabetes than in healthy controls.

Limitations

Animal group sizes and the size and composition of the human comparison are not reported in the abstract; the human component is cross-sectional and correlational, and senescence endpoints are surrogate markers rather than diabetes outcomes.

Study record

Annotated fields for this study
Study modelAnimal study (in vivo)
Substance studiedSeveralMore than one of these is central to the paper (common for reviews).
Speciesmouse, human
System studiedAged C57BL/6 mouse pancreatic islets, S961-treated C57BL/6 mice and nonobese diabetic mice; circulating MOTS-c in people with type 2 diabetes
Populationpeople with type 2 diabetes and healthy controls (circulating MOTS-c comparison)
DesignControlled animal experiment with isolated islet treatment and a human biomarker comparison
Sample size as reportednot reported
Control groupuntreated aged islets and untreated S961-treated and nonobese diabetic mice; healthy human controls
Route (data field only)Not reported
Endpoints measuredislet MOTS-c levels; islet cell senescence markers; nuclear gene expression; metabolites of beta-cell senescence; glucose intolerance; circulating MOTS-c in humans
Pathways measuredInsulin & glucose handling · Nuclear translocation
Research areasMetabolic · Aging · Mitochondrial biology
Evidence tierC — Animal in vivo
Publication typesJournal Article

Appraisal

Each dimension is recorded separately and never combined into a single score. A study can be well controlled and still tell you little about people.

Relevance to MOTS-c
Direct
Model applicability
Mammalian
Sample size
Not reported
Controls
Appropriate
Outcome validity
Surrogate
Support for its own conclusion
Moderate

Provenance

  • Bibliographic fields retrieved from PubMed E-utilities efetch (title, journal, date, authors, DOI) on 2026-11-11.
  • Annotated from the published abstract.
  • Editorial review: approved (2026-11-11).
  • Classification follows the site methodology; the record describes the study, not what MOTS-c does in people.