Evidence map›Paper›PMID 38881280›Full record

ArticleAging cell2024

Age-specific and compartment-dependent changes in mitochondrial homeostasis and cytoplasmic viscosity in mouse peripheral neurons.

James N Sleigh, Francesca Mattedi, Sandy Richter, Emily Annuario, Kristal Ng, I Emilie Steinmark, Iveta Ivanova, István L Darabán, Parth P Joshi, Elena R Rhymes and 6 more

Abstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

James N SleighDepartment of Neuromuscular Diseases and UCL Queen Square Motor Neuron Disease Centre, UCL Queen Square Institute of Neurology, University College London, London, UK.ORCID 0000-0002-3782-9045
Francesca MattediDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0002-0306-5796
Sandy RichterDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0003-2496-9337
Emily AnnuarioDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0002-0342-1113
Kristal NgDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0003-2301-8206
I Emilie SteinmarkDepartment of Physics, King's College London, London, UK.ORCID 0000-0002-7024-8736
Iveta IvanovaDepartment of Physics, King's College London, London, UK.
István L DarabánDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Parth P JoshiDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Elena R RhymesDepartment of Neuromuscular Diseases and UCL Queen Square Motor Neuron Disease Centre, UCL Queen Square Institute of Neurology, University College London, London, UK.ORCID 0000-0002-7103-5513
Shirwa AwaleDepartment of Physics, King's College London, London, UK.
Gokhan YahiogluAntikor Biopharma Ltd, Stevenage Bioscience Catalyst, Stevenage, UK.ORCID 0000-0003-4043-4914
Jacqueline C MitchellDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0002-2677-398X
Klaus SuhlingDepartment of Physics, King's College London, London, UK.
Giampietro SchiavoDepartment of Neuromuscular Diseases and UCL Queen Square Motor Neuron Disease Centre, UCL Queen Square Institute of Neurology, University College London, London, UK.ORCID 0000-0002-4319-8745
Alessio VagnoniDepartment of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.ORCID 0000-0003-2947-9193

Funding

Academy of Medical Sciences SBF004/1088Alzheimer's Research UK ARUK-NC2020-KCLBiotechnology and Biological Sciences Research Council BB/R004803/1Biotechnology and Biological Sciences Research Council BB/T508597/1British Society for Cell BiologyHorizon 2020 Framework Programme 857524John and Lucille Van Geest FoundationMedical Research Council MR/S006990/1Medical Research Council MR/Y010949/1National Centre for the Replacement Refinement and Reduction of Animals in Research NC/N001753/2National Centre for the Replacement Refinement and Reduction of Animals in Research NC/T001224/1Royal Society RGS\R2\180450The Sigrid Rausing TrustUK Dementia Research Institute UKDRI-1005Wellcome TrustWellcome Trust 103191/A/13/ZWellcome Trust 107116/Z/15/ZWellcome Trust 204823/Z/16/ZWellcome Trust 223022/Z/21/Z
6 · The paper itself

Abstract

Mitochondria are dynamic bioenergetic hubs that become compromised with age. In neurons, declining mitochondrial axonal transport has been associated with reduced cellular health. However, it is still unclear to what extent the decline of mitochondrial transport and function observed during ageing are coupled, and if somal and axonal mitochondria display compartment-specific features that make them more susceptible to the ageing process. It is also not known whether the biophysical state of the cytoplasm, thought to affect many cellular functions, changes with age to impact mitochondrial trafficking and homeostasis. Focusing on the mouse peripheral nervous system, we show that age-dependent decline in mitochondrial trafficking is accompanied by reduction of mitochondrial membrane potential and intramitochondrial viscosity, but not calcium buffering, in both somal and axonal mitochondria. Intriguingly, we observe a specific increase in cytoplasmic viscosity in the neuronal cell body, where mitochondria are most polarised, which correlates with decreased cytoplasmic diffusiveness. Increasing cytoplasmic crowding in the somatic compartment of DRG neurons grown in microfluidic chambers reduces mitochondrial axonal trafficking, suggesting a mechanistic link between the regulation of cytoplasmic viscosity and mitochondrial dynamics. Our work provides a reference for studying the relationship between neuronal mitochondrial homeostasis and the viscoelasticity of the cytoplasm in a compartment-dependent manner during ageing.

Indexed as

CytoplasmHomeostasisMitochondriaNeuronsAgingAnimalsMiceMice, Inbred C57BLViscosityadvanced microscopyageingaxonal transportcrowding and viscosityFLIMmicemitochondriaTR‐FAIM

Identifiers

PMID38881280
PMCPMC11464114

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.