Evidence map›Paper›PMID 33154382›Full record

ArticleNature communications2020

Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS.

Veselina Petrova, Craig S Pearson, Jared Ching, James R Tribble, Andrea G Solano, Yunfei Yang, Fiona M Love, Robert J Watt, Andrew Osborne, Evan Reid and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
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  8. Genetic engineering and the eye.Eye (London, England) · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. The Endoplasmic Reticulum and Its Contacts: Emerging Roles in Axon Development, Neurotransmission, and Degeneration.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2024
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Protrudin-mediated ER-endosome contact sites promote phagocytosis.Cellular and molecular life sciences : CMLS · 2023
    Article
  18. Integrin-Driven Axon Regeneration in the Spinal Cord Activates a Distinctive CNS Regeneration Program.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  19. Regulation of axonal regeneration after mammalian spinal cord injury.Nature reviews. Molecular cell biology · 2023
    Review
  20. Article
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

15 authors at 5 institutions in 6 countries.

Veselina PetrovaJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK. vp351@cam.ac.uk.ORCID 0000-0002-5593-0198
Craig S PearsonLaboratory of Developmental Neurobiology, Division of Intramural Research, National Heart, Lung and Blood Institute, NIH, Bethesda, USA.
Jared ChingJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
James R TribbleDepartment of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden.
Andrea G SolanoLaboratory of Developmental Neurobiology, Division of Intramural Research, National Heart, Lung and Blood Institute, NIH, Bethesda, USA.
Yunfei YangDepartment of Ophthalmology, Addenbrooke's Hospital, Cambridge, UK.ORCID 0000-0002-7130-9801
Fiona M LoveJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0002-7805-5234
Robert J WattJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Andrew OsborneJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
Evan ReidCambridge Institute for Medical Research and Department of Medical Genetics, University of Cambridge, Cambridge, UK.ORCID 0000-0003-1623-7304
Pete A WilliamsDepartment of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-6194-8397
Keith R MartinJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0002-9347-3661
Herbert M GellerLaboratory of Developmental Neurobiology, Division of Intramural Research, National Heart, Lung and Blood Institute, NIH, Bethesda, USA.ORCID 0000-0002-7048-6144
Richard EvaJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK. re263@cam.ac.uk.ORCID 0000-0003-0305-0452
James W FawcettJohn van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK. jf108@cam.ac.uk.ORCID 0000-0002-7990-4568
University of Cambridge · GBNational Heart Lung and Blood Institute · USKarolinska Institutet · SEAddenbrooke's Hospital · GBThe University of Melbourne · AU

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
Medical Research Council MR/R004463/1Medical Research Council MR/R004544/1NIGMS NIH HHS T32 GM007200Wellcome Trust 082381
6 · The paper itself

Abstract

Adult mammalian central nervous system axons have intrinsically poor regenerative capacity, so axonal injury has permanent consequences. One approach to enhancing regeneration is to increase the axonal supply of growth molecules and organelles. We achieved this by expressing the adaptor molecule Protrudin which is normally found at low levels in non-regenerative neurons. Elevated Protrudin expression enabled robust central nervous system regeneration both in vitro in primary cortical neurons and in vivo in the injured adult optic nerve. Protrudin overexpression facilitated the accumulation of endoplasmic reticulum, integrins and Rab11 endosomes in the distal axon, whilst removing Protrudin's endoplasmic reticulum localization, kinesin-binding or phosphoinositide-binding properties abrogated the regenerative effects. These results demonstrate that Protrudin promotes regeneration by functioning as a scaffold to link axonal organelles, motors and membranes, establishing important roles for these cellular components in mediating regeneration in the adult central nervous system.

Indexed as

Nerve RegenerationAnimalsAxonsCells, CulturedCentral Nervous SystemEndoplasmic ReticulumEndosomesFemaleHumansIntegrinsMiceMice, Inbred C57BLMutationNeuronsNeuroprotective AgentsOptic Nerve InjuriesIntegrinsNeuroprotective AgentsVesicular Transport ProteinsZFYVE27 protein, human

Identifiers

PMID33154382
PMCPMC7645621
OpenAlexW3096302962

What OpenQuestion holds

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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.