Evidence map›Paper›PMID 32778834›Full record

ArticleNature metabolism2020

AMPK controls the axonal regenerative ability of dorsal root ganglia sensory neurons after spinal cord injury.

Guiping Kong, Luming Zhou, Elisabeth Serger, Ilaria Palmisano, Francesco De Virgiliis, Thomas H Hutson, Eilidh Mclachlan, Anja Freiwald, Paolo La Montanara, Kirill Shkura and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% of its field
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Review
  9. Deletion ofFrontiers in behavioral neuroscience · 2025
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  12. CaeNeuro · 2024
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  13. Review
  14. Impaired end joining induces cardiac atrophy in a Hutchinson-Gilford progeria mouse model.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Circular RNAs in organ injury: recent development.Journal of translational medicine · 2022
    Review
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

12 authors at 4 institutions in 2 countries.

Guiping Kong *Division of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
Luming Zhou *Division of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
Elisabeth SergerDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
Ilaria PalmisanoDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-7139-8090
Francesco De VirgiliisDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
Thomas H HutsonDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-6795-2688
Eilidh MclachlanDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
Anja FreiwaldProteomics Core Facility, Institute of Molecular Biology, Mainz, Germany.
Paolo La MontanaraDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
Kirill ShkuraDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-1722-0910
Radhika PuttaguntaHertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-7674-8064
Simone Di GiovanniDivision of Neuroscience, Department of Brain Sciences, Imperial College London, London, UK. s.di-giovanni@imperial.ac.uk.ORCID http://orcid.org/0000-0003-3154-5399
Imperial College London · GBHertie Institute for Clinical Brain Research · DEHeidelberg University · DEInstitute of Molecular Biology · DE

Funding

Department of HealthMedical Research Council
6 · The paper itself

Abstract

Regeneration after injury occurs in axons that lie in the peripheral nervous system but fails in the central nervous system, thereby limiting functional recovery. Differences in axonal signalling in response to injury that might underpin this differential regenerative ability are poorly characterized. Combining axoplasmic proteomics from peripheral sciatic or central projecting dorsal root ganglion (DRG) axons with cell body RNA-seq, we uncover injury-dependent signalling pathways that are uniquely represented in peripheral versus central projecting sciatic DRG axons. We identify AMPK as a crucial regulator of axonal regenerative signalling that is specifically downregulated in injured peripheral, but not central, axons. We find that AMPK in DRG interacts with the 26S proteasome and its CaMKIIα-dependent regulatory subunit PSMC5 to promote AMPKα proteasomal degradation following sciatic axotomy. Conditional deletion of AMPKα1 promotes multiple regenerative signalling pathways after central axonal injury and stimulates robust axonal growth across the spinal cord injury site, suggesting inhibition of AMPK as a therapeutic strategy to enhance regeneration following spinal cord injury.

Indexed as

AxonsNerve RegenerationAMP-Activated Protein KinasesAnimalsATPases Associated with Diverse Cellular ActivitiesAxonal TransportAxotomyCalcium-Calmodulin-Dependent Protein Kinase Type 2FemaleGanglia, SpinalMiceMice, Inbred C57BLProteasome Endopeptidase ComplexProteomicsSciatic NerveSensory Receptor CellsAMP-Activated Protein KinasesATPases Associated with Diverse Cellular ActivitiesCalcium-Calmodulin-Dependent Protein Kinase Type 2Proteasome Endopeptidase ComplexPsmc5 protein, mouse

Identifiers

PMID32778834
OpenAlexW3047938199

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.