bioRxivCell BiologyPreprint
Inhibition of Mitochondrial Respiration Fragments ER Architecture and Remodels Organelle Contact Sites, as Revealed by FIB-SEM
Andrea DlaskováiD, Bazila BazilaiD, Pavel KřepelkaiD, Rhea Christine Victor, Darsh Jaresh Jhala, Petr JežekiD
Abstract
The endoplasmic reticulum (ER) and mitochondria maintain a dynamic structural partnership essential for pancreatic {beta}-cell homeostasis, yet the high-resolution 3D remodeling of these networks under stress conditions remains poorly defined. We employed Focused Ion Beam Scanning Electron Microscopy (FIB-SEM) to perform 3D reconstructions of INS1E cells subjected to mitochondrial respiratory chain inhibition, uncoupling, and exogenous oxidative stress. Quantitative analysis revealed that mitochondrial dysfunction induces profound ultrastructural transitions, characterized by significant luminal swelling of the ER, expansion of the perinuclear space, and mitochondrial diameter enlargement. 3D volume imaging identified a coordinated fragmentation of both ER and mitochondrial networks into discrete, spatially separated structures--a phenomenon distinct from the reticular morphology observed in control cells. The similarity between respiratory inhibition- and H2O2-induced phenotypes, together with preservation of ER structure following mitochondrial uncoupling, suggests a potential contribution of reactive oxygen species to the observed remodeling process. Despite this extensive organelle breakdown, interorganelle membrane contact sites were not only preserved but expanded under stress conditions. We further provide a quantitative description of nuclear envelope-mitochondria contact sites (NAMs), demonstrating their selective remodeling during mitochondrial dysfunction. Our findings provide a high-resolution structural framework for organelle remodeling in {beta}-cells, demonstrating that membrane contact sites are actively preserved and reorganized despite profound organelle fragmentation. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=110 SRC="FIGDIR/small/727587v1_ufig1.gif" ALT="Figure 1"> View larger version (36K): org.highwire.dtl.DTLVardef@4f63b5org.highwire.dtl.DTLVardef@1b3dc8org.highwire.dtl.DTLVardef@7527fcorg.highwire.dtl.DTLVardef@1944f2c_HPS_FORMAT_FIGEXP M_FIG C_FIG
- organism: mouse
- assay: imaging
- research focus: cell type annotation
- research focus: cell signaling & trafficking
- research focus: development & morphogenesis
- research focus: metabolism & bioenergetics
- approach: microscopy & imaging analysis
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A non-canonical unfolded protein response pathway and mitochondrial dynamics control the number of ER-mitochondria contact sites
R. Kojima, Y. Kakimoto, … Y. Tamura·bioRxiv·Jun 27, 2019
- Motion of single molecular tethers reveals dynamic subdomains at ER-mitochondria contact sites
C. J. Obara, J. Nixon-Abell, … J. Lippincott-Schwartz·bioRxiv·Sep 3, 2022
- ER-Mitochondria Contact Sites expand during mitosis
F. Yu, R. Courjaret, … K. Machaca·bioRxiv·Jun 22, 2023
- Active control of mitochondrial network morphology by metabolism driven redox state
Gaurav Singh, Vineeth Vengayil, … Sunil Laxman·Proceedings of the National Academy of SciencesPeer-reviewed·Apr 17, 2025
- Three-dimensional ATUM-SEM reconstruction and analysis of hepatic endoplasmic reticulum-organelle interactions
- Morphotype-Resolved 3D Morphometry Reveals a Structure-Density-Location Coupling in Mitochondrial Networks
Anshu Singh, Arun Yadav, … Jitin Singla·StructurePeer-reviewed·Aug 20, 2026