Evidence map›Paper›PMID 25869803›Full record

ArticleMolecular psychiatry2015

Neurofilament subunits are integral components of synapses and modulate neurotransmission and behavior in vivo.

A Yuan, H Sershen, Veeranna, B S Basavarajappa, A Kumar, A Hashim, M Berg, J-H Lee, Y Sato, M V Rao and 5 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 123 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Control of Schwann Cell Myelination by DDR1 Receptor Tyrosine Kinase.International journal of molecular sciences · 2026
    Article
  4. Review
  5. Review
  6. Neuronal Calcium Signaling and Cytoskeletal Dynamics in Neurodegeneration.International journal of molecular sciences · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Frontotemporal Dementia, Where Do We Stand? A Narrative Review.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Article

15 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

A Yuan1] Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, New York University School of Medicine, New York, NY, USA.
H Sershen1] Department of Psychiatry, New York University School of Medicine, New York, NY, USA [2] Neurochemistry Division, Nathan Kline Institute, Orangeburg, NY, USA.
Veeranna1] Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, New York University School of Medicine, New York, NY, USA.
B S Basavarajappa1] Analytical Psychopharmacology Division, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, College of Physicians & Surgeons, Columbia University, New York, NY, USA.
A Kumar1] Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, New York University School of Medicine, New York, NY, USA.
A HashimNeurochemistry Division, Nathan Kline Institute, Orangeburg, NY, USA.
M BergCenter for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA.
J-H Lee1] Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, New York University School of Medicine, New York, NY, USA.
Y SatoCenter for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA.
M V Rao1] Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, New York University School of Medicine, New York, NY, USA.
P S MohanCenter for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA.
V DyakinCenter for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA.
J-P JulienCentre de Recherche du Centre Hospitalier de l'Université Laval, Département d'anatomie et physiologie de l'Université Laval, Québec, QC, Canada.
V M-Y LeeDepartment of Pathology & Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
R A Nixon1] Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY, USA [2] Department of Psychiatry, New York University School of Medicine, New York, NY, USA [3] Department of Cell Biology, New York University School of Medicine, New York, NY, USA.
Nathan Kline Institute for Psychiatric Research · USUniversity of Pennsylvania · US

Funding

DYNAMICS OF THE NEURONAL CYTOSKELETON IN AGING BRAINR01AG005604 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NIXON, RALPH A. · 1985 to 2014
$4.5M
Endocannabinoid Signaling in Postnatal Ethanol EffectsR01AA019443 · NIAAA · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI BALAPAL, BASAVARAJ S · 2010 to 2019
$3.2M
NIAAA NIH HHS R01 AA019443NIA NIH HHS 5R01AG005604NIA NIH HHS R01 AG005604
6 · The paper itself

Abstract

Synaptic roles for neurofilament (NF) proteins have rarely been considered. Here, we establish all four NF subunits as integral resident proteins of synapses. Compared with the population in axons, NF subunits isolated from synapses have distinctive stoichiometry and phosphorylation state, and respond differently to perturbations in vivo. Completely eliminating NF proteins from brain by genetically deleting three subunits (α-internexin, NFH and NFL) markedly depresses hippocampal long-term potentiation induction without detectably altering synapse morphology. Deletion of NFM in mice, but not the deletion of any other NF subunit, amplifies dopamine D1-receptor-mediated motor responses to cocaine while redistributing postsynaptic D1-receptors from endosomes to plasma membrane, consistent with a specific modulatory role of NFM in D1-receptor recycling. These results identify a distinct pool of synaptic NF subunits and establish their key role in neurotransmission in vivo, suggesting potential novel influences of NF proteins in psychiatric as well as neurological states.

Indexed as

AnimalsAxonsBrainCocaineDopamine Uptake InhibitorsLong-Term PotentiationMice, KnockoutMotor ActivityNeurofilament ProteinsReceptors, Dopamine D1SynapsesSynaptic TransmissionCocaineDopamine Uptake InhibitorsDrd1 protein, mouseNeurofilament ProteinsReceptors, Dopamine D1

Identifiers

PMID25869803
PMCPMC4514553
OpenAlexW2044444144

What OpenQuestion holds

Textmetadata
LicenceTDM
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.