Super-resolution microscopies, technological breakthrough to decipher mitochondrial structure and dynamic.

ElsevierVolumes 159–160, June–July 2024, Pages 38-51Seminars in Cell & Developmental BiologyAuthor links open overlay panel, , Abstract

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?

AbbreviationsCSM

Confocal Scanning Microscopy

DNA-PAINT

DNA-based Point Accumulation for Imaging in Nanoscale Topography

DRP1

dynamin-related protein 1

MAM

mitochondria-associated membrane

MFN1/MFN2

mitofusin 1/mitofusin 2

MICOS

mitochondrial contact site and cristae organising system

MINFLUX

MINimal photon FLUXes

MOMP

mitochondrial outer membrane permeabilization

∆Ψm

mitochondrial membrane potential

NL-SIM

non-linear illumination patterns

OXPHOS

oxidative phosphorylation

PA-FP

photo-activable fluorescent protein

PALM

PhotoActivation Localisation Microscopy

RESOLFT

REversible Saturable OpticaL Fluorescence Transition

ROS

Reactive Oxygen Species

SIM

Structured Illumination Microscopy

SMLM

Single Molecule Localisation Microscopy

SPT

Single particle tracking

STED

STimulated Emission Depletion

dSTORM

(direct) Stochastic Optical Reconstruction Microscopy

TIRF

Total Internal Reflection Fluorescence

Keywords

Mitochondria

Nucleoids

Microscopy

Super-resolution

MICOS

© 2024 The Author(s). Published by Elsevier Ltd.

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