Mitochondria are complex organelles with an outer membrane enveloping a second inner membrane that creates a vast matrix space partitioned by pockets or cristae that join the peripheral inner membrane with several thin junctions. Several micrometres long, mitochondria are generally close to 300 nm in diameter, with membrane layers separated by a few tens of nanometres. Ultrastructural data from electron microscopy revealed the structure of these mitochondria, while conventional optical microscopy revealed their extraordinary dynamics through fusion, fission, and migration processes but its limited resolution power restricted the possibility to go further. By overcoming the limits of light diffraction, Super-Resolution Microscopy (SRM) now offers the potential to establish the links between the ultrastructure and remodelling of mitochondrial membranes, leading to major advances in our understanding of mitochondria’s structure-function. Here we review the contributions of SRM imaging to our understanding of the relationship between mitochondrial structure and function. What are the hopes for these new imaging approaches which are particularly important for mitochondrial pathologies?
AbbreviationsCSMConfocal Scanning Microscopy
DNA-PAINTDNA-based Point Accumulation for Imaging in Nanoscale Topography
DRP1dynamin-related protein 1
MAMmitochondria-associated membrane
MFN1/MFN2mitofusin 1/mitofusin 2
MICOSmitochondrial contact site and cristae organising system
MINFLUXMINimal photon FLUXes
MOMPmitochondrial outer membrane permeabilization
∆Ψmmitochondrial membrane potential
NL-SIMnon-linear illumination patterns
OXPHOSoxidative phosphorylation
PA-FPphoto-activable fluorescent protein
PALMPhotoActivation Localisation Microscopy
RESOLFTREversible Saturable OpticaL Fluorescence Transition
ROSReactive Oxygen Species
SIMStructured Illumination Microscopy
SMLMSingle Molecule Localisation Microscopy
SPTSingle particle tracking
STEDSTimulated Emission Depletion
dSTORM(direct) Stochastic Optical Reconstruction Microscopy
TIRFTotal Internal Reflection Fluorescence
KeywordsMitochondria
Nucleoids
Microscopy
Super-resolution
MICOS
© 2024 The Author(s). Published by Elsevier Ltd.
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