Study record

Mitofusion is required for MOTS-c induced GLUT4 translocation

Bhullar KS, Shang N, Kerek E et al. · Sci Rep · 2021

CellsMOTS-c administeredEvidence tier D

What this study reported

Reported that MOTS-c treatment of mammalian cells increased mitochondrial biogenesis markers TFAM, COX4 and NRF1 while flow cytometry showed a lower mitochondrial count, and increased the fusion GTPases OPA1 and MFN2. Blocking these GTPases with TNF-alpha or knocking down MFN2 abolished MOTS-c-associated GLUT4 translocation and glucose uptake.

Limitations

Entirely cell-based with no in vivo confirmation; mitochondrial counting relies on a single dye-based flow cytometry method, and TNF-alpha is a non-specific tool for inhibiting fusion.

Study record

Annotated fields for this study
Study modelCell study (in vitro)
Substance studiedMOTS-c administeredSynthetic MOTS-c was given to cells, animals or people.
Specieshuman, mouse
System studiedMammalian cell lines including HEK293 and adipocytes treated with MOTS-c, with siRNA knockdown of MFN2
PopulationNot reported
DesignCell culture experiments
Sample size as reportedNot reported
Control groupuntreated cells and non-targeting siRNA controls
Route (data field only)in-culture
Endpoints measuredTFAM, COX4 and NRF1 levels; mitochondrial count by flow cytometry; OPA1 and MFN2 levels; GLUT4 translocation; glucose uptake
Pathways measuredInsulin & glucose handling · SIRT1 / PGC-1α / biogenesis · Other
Research areasMetabolic · Mitochondrial biology
Evidence tierD — Cell, tissue or analytical
Publication typesJournal Article, Research Support, Non-U.S. Gov't

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
Cellular
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.