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Mitochondria are dynamic and motile organelles that respond rapidly to oxidative stress
and cellular energy demands. Their morphological changes, as determined by fission
and fusion, have been linked to the progression of neuropathic pain. However, little
is known about specific pathology underlying mitochondrial dysfunction after peripheral
nerve injury or how pharmacological interventions affect these changes. Our goal is
to evaluate mitochondrial dynamics following peripheral nerve injury by characterizing
axonal mitochondrial density, movement in axons and fusion-fission events. We dissociated
dorsal root ganglia (DRG) from mice with spare nerve injury (SNI) and selectively
labelled mitochondria with a live-cell fluorescent dye. Time lapse videos were then
captured using a spinning disk confocal microscope. We observed a significant increase
in axonal mitochondrial density in DRG cultures obtained from SNI mice when compared
to naïve cultures. Representative kymograph images depict a larger proportion of mitochondria
moving anterogradely in axons of DRG neurons from SNI mice. Interestingly, we found
that the SNI-mitochondria are trafficked at lower velocities. Previous studies have
shown that calcium overload in damaged mitochondria may contribute to decreased mitochondrial
motility. Additionally, we observe a decrease in perinuclear clustering within the
SNI group which may indicate a disruption in mitochondrial networking or a failure
to regulate fission events in DRG neurons after injury. Collectively, our findings
highlight the benefit of real time imaging of DRG neurons to gain greater insight
into specific aspects of mitochondrial dysfunction after nerve injury. Our findings
likely have important implications for therapeutic approaches to neuropathic pain.
Supported by NIH grant NS065926.
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© 2022 Published by Elsevier Inc.