Evidence map›Paper›PMID 24782707›Full record

ArticleFrontiers in cellular neuroscience2014

The spatiotemporal organization of cerebellar network activity resolved by two-photon imaging of multiple single neurons.

Daniela Gandolfi, Paolo Pozzi, Marialuisa Tognolina, Giuseppe Chirico, Jonathan Mapelli, Egidio D'Angelo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Hyperexcitability and Hyperplasticity Disrupt Cerebellar Signal Transfer in theThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Heterosynaptic GABAergic plasticity bidirectionally driven by the activity of pre- and postsynaptic NMDA receptors.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  17. Article
  18. Review
  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

6 authors at 3 institutions in 1 country.

Daniela GandolfiLaboratory of Neurophysiology, Department of Brain and Behavioral Sciences, University of Pavia Pavia, Italy ; Laboratory of Experimental and Computational Neurophysiology, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia Modena, Italy.
Paolo PozziLaboratory of Biophysics and Biophotonics, Department of Physics, University of Milano-Bicocca Milano, Italy.
Marialuisa TognolinaLaboratory of Neurophysiology, Department of Brain and Behavioral Sciences, University of Pavia Pavia, Italy.
Giuseppe ChiricoLaboratory of Biophysics and Biophotonics, Department of Physics, University of Milano-Bicocca Milano, Italy.
Jonathan MapelliLaboratory of Experimental and Computational Neurophysiology, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia Modena, Italy ; Laboratory of Neurophysiology, Brain Connectivity Center, C. Mondino National Neurological Institute, Fondazione IRCCS C. Mondino Pavia, Italy.
Egidio D'AngeloLaboratory of Neurophysiology, Department of Brain and Behavioral Sciences, University of Pavia Pavia, Italy ; Laboratory of Neurophysiology, Brain Connectivity Center, C. Mondino National Neurological Institute, Fondazione IRCCS C. Mondino Pavia, Italy.
Fondazione Istituto Neurologico Nazionale Casimiro Mondino · ITUniversity of Milano-Bicocca · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to investigate the spatiotemporal organization of neuronal activity in local microcircuits, techniques allowing the simultaneous recording from multiple single neurons are required. To this end, we implemented an advanced spatial-light modulator two-photon microscope (SLM-2PM). A critical issue for cerebellar theory is the organization of granular layer activity in the cerebellum, which has been predicted by single-cell recordings and computational models. With SLM-2PM, calcium signals could be recorded from different network elements in acute cerebellar slices including granule cells (GrCs), Purkinje cells (PCs) and molecular layer interneurons. By combining WCRs with SLM-2PM, the spike/calcium relationship in GrCs and PCs could be extrapolated toward the detection of single spikes. The SLM-2PM technique made it possible to monitor activity of over tens to hundreds neurons simultaneously. GrC activity depended on the number of spikes in the input mossy fiber bursts. PC and molecular layer interneuron activity paralleled that in the underlying GrC population revealing the spread of activity through the cerebellar cortical network. Moreover, circuit activity was increased by the GABA-A receptor blocker, gabazine, and reduced by the AMPA and NMDA receptor blockers, NBQX and APV. The SLM-2PM analysis of spatiotemporal patterns lent experimental support to the time-window and center-surround organizing principles of the granular layer.

Indexed as

cerebellumgranule cellsPurkinje cellstwo-photon microscopy

Identifiers

PMID24782707
PMCPMC3995049
OpenAlexW2058681228

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.