Evidence map›Paper›PMID 28119345›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2017

Heparan Sulfates Support Pyramidal Cell Excitability, Synaptic Plasticity, and Context Discrimination.

Daniel Minge, Oleg Senkov, Rahul Kaushik, Michel K Herde, Olga Tikhobrazova, Andreas B Wulff, Andrey Mironov, Toin H van Kuppevelt, Arie Oosterhof, Gaga Kochlamazashvili and 2 more

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Rapid Fluorescence Lifetime Imaging Reveals That TRPV4 Channels Promote Dysregulation of Neuronal NaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Local Resting CaCell reports · 2020
    Article
  14. Quantitative determination of cellular [NaThe Journal of general physiology · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

12 authors.

Daniel MingeInstitute of Cellular Neurosciences, University of Bonn Medical School, 53105 Bonn, Germany.
Oleg SenkovGerman Center for Neurodegenerative Diseases (DZNE), 39120 Magdeburg, Germany.
Rahul KaushikGerman Center for Neurodegenerative Diseases (DZNE), 39120 Magdeburg, Germany.
Michel K HerdeInstitute of Cellular Neurosciences, University of Bonn Medical School, 53105 Bonn, Germany.
Olga TikhobrazovaDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, 16163 Genova, Italy.
Andreas B WulffInstitute of Cellular Neurosciences, University of Bonn Medical School, 53105 Bonn, Germany.
Andrey MironovDepartment of Neurotechnology, Lobachevsky State University of Nizhny Novgorod, 603950 Nizhny Novgorod, Russia.
Toin H van KuppeveltDepartment of Biochemistry, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Arie OosterhofDepartment of Biochemistry, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Gaga KochlamazashviliDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, 16163 Genova, Italy.
Alexander DityatevGerman Center for Neurodegenerative Diseases (DZNE), 39120 Magdeburg, Germany.
Christian HennebergerInstitute of Cellular Neurosciences, University of Bonn Medical School, 53105 Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heparan sulfate (HS) proteoglycans represent a major component of the extracellular matrix and are critical for brain development. However, their function in the mature brain remains to be characterized. Here, acute enzymatic digestion of HS side chains was used to uncover how HSs support hippocampal function in vitro and in vivo. We found that long-term potentiation (LTP) of synaptic transmission at CA3-CA1 Schaffer collateral synapses was impaired after removal of highly sulfated HSs with heparinase 1. This reduction was associated with decreased Ca2+ influx during LTP induction, which was the consequence of a reduced excitability of CA1 pyramidal neurons. At the subcellular level, heparinase treatment resulted in reorganization of the distal axon initial segment, as detected by a reduction in ankyrin G expression. In vivo, digestion of HSs impaired context discrimination in a fear conditioning paradigm and oscillatory network activity in the low theta band after fear conditioning. Thus, HSs maintain neuronal excitability and, as a consequence, support synaptic plasticity and learning.

Indexed as

AnimalsAnkyrinsCA1 Region, HippocampalCA3 Region, HippocampalCalcium SignalingConditioning, PsychologicalDiscrimination, PsychologicalFearHeparan SulfateHeparin LyaseIn Vitro TechniquesLong-Term PotentiationMaleMiceMice, Inbred C57BLNerve NetAnk3 protein, mouseAnkyrinsHeparan SulfateHeparin Lyaseextracellular matrixheparan sulfateslearningneuronal excitabilitysynaptic plasticity

Identifiers

PMID28119345
PMCPMC5390399

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.