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Updated: Jun 27, 2026

Visualization of Endogenous Mitophagy Complexes In Situ in Human Pancreatic Beta Cells Utilizing Proximity Ligation Assay
Published on: May 2, 2019
Autophagy and VMP1 expression are early cellular events in experimental diabetes
Daniel Grasso1, Maria L Sacchetti, Lidia Bruno
1Department of Physiology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.
Background/Aims:
We have described VMP1 as a new protein which expression triggers autophagy in mammalian cells. Here we show that experimental diabetes activates VMP1 expression and autophagy in pancreas beta cells as a direct response to streptozotocin (STZ).
Methods:
Male Wistar rats were treated with 65 mg/kg STZ and pancreas islets from untreated rats were incubated with 1 mM STZ.
Results:
RT-PCR analysis shows early VMP1 induction after STZ treatment. In situ hybridization reveals VMP1 mRNA in islet beta cells. Electron microscopy shows chromatin aggregation and autophagy morphology that was confirmed by LC3 expression and LC3-VMP1 co-localization. Apoptotic cell death and the reduction of beta cell pool are evident after 24 h treatment, while VMP1 is still expressed in the remaining cells. VMP1-Beclin1 colocalization in pancreas tissue from STZ-treated rats suggests that VMP1-Beclin1 interaction is involved in the autophagic process activation during experimental diabetes. Results were confirmed using pancreas islets, showing VMP1 expression and autophagy in beta cells as a direct effect of STZ treatment.
Conclusion:
Pancreas beta cells trigger VMP1 expression and autophagy during the early cellular events in response to experimental diabetes.
Insights
Experimental diabetes activates VMP1 protein expression and autophagy in pancreas beta cells. This study reveals VMP1
Area of Science:
- Cell Biology
- Endocrinology
- Molecular Biology
Background:
- The VMP1 protein is known to trigger autophagy in mammalian cells.
- Experimental diabetes induced by streptozotocin (STZ) activates VMP1 expression and autophagy in pancreas beta cells.
Purpose of the Study:
- To investigate the role of VMP1 in the cellular response to experimental diabetes in pancreas beta cells.
- To confirm VMP1's role in STZ-induced autophagy.
Main Methods:
- Streptozotocin (STZ) treatment in male Wistar rats and isolated rat pancreas islets.
- Reverse transcription-polymerase chain reaction (RT-PCR) for VMP1 induction.
- In situ hybridization for VMP1 mRNA localization.
- Electron microscopy for autophagy morphology.
- LC3 and VMP1 expression analysis and co-localization studies.
Main Results:
- STZ treatment rapidly induced VMP1 expression in pancreas beta cells.
- Autophagy morphology, confirmed by LC3 expression and LC3-VMP1 co-localization, was observed.
- Apoptotic cell death and beta cell loss occurred, with VMP1 expression persisting in remaining cells.
- VMP1-Beclin1 co-localization suggested involvement in autophagic process activation.
Conclusions:
- Pancreas beta cells activate VMP1 expression and autophagy in response to experimental diabetes.
- VMP1 plays a role in the early cellular events during experimental diabetes.
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