Evidence map›Paper›PMID 30929054›Full record

ArticleBrain structure & function2019

Variability and directionality of inferior olive neuron dendrites revealed by detailed 3D characterization of an extensive morphological library.

Nora Vrieler, Sebastian Loyola, Yasmin Yarden-Rabinowitz, Jesse Hoogendorp, Nikolay Medvedev, Tycho M Hoogland, Chris I De Zeeuw, Erik De Schutter, Yosef Yarom, Mario Negrello and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Structural and Functional Organization of Visual Responses in the Inferior Olive of Larval Zebrafish.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Dendritic Architecture PredictsFrontiers in neural circuits · 2021
    Article
  11. Article
  12. Article
  13. Review
  14. Role of cerebellar GABAergic dysfunctions in the origins of essential tremor.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Quasiperiodic rhythms of the inferior olive.PLoS computational biology · 2019
    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 at 5 institutions in 4 countries.

Nora VrielerDepartment of Neurobiology, Institute of Life Sciences and Edmond and Lily Safra Center for Brain Sciences, Hebrew University, Jerusalem, Israel.ORCID http://orcid.org/0000-0002-8008-7884
Sebastian LoyolaNetherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.
Yasmin Yarden-RabinowitzDepartment of Neurobiology, Institute of Life Sciences and Edmond and Lily Safra Center for Brain Sciences, Hebrew University, Jerusalem, Israel.ORCID http://orcid.org/0000-0001-5507-9180
Jesse HoogendorpNetherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.
Nikolay MedvedevComputational Neuroscience Unit, Okinawa Institute of Science and Technology Graduate University, Onna, Okinawa, 904-0495, Japan.ORCID http://orcid.org/0000-0002-6428-5290
Tycho M HooglandNetherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.
Chris I De ZeeuwNetherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5628-8187
Erik De SchutterComputational Neuroscience Unit, Okinawa Institute of Science and Technology Graduate University, Onna, Okinawa, 904-0495, Japan.ORCID http://orcid.org/0000-0001-8618-5138
Yosef YaromDepartment of Neurobiology, Institute of Life Sciences and Edmond and Lily Safra Center for Brain Sciences, Hebrew University, Jerusalem, Israel.ORCID http://orcid.org/0000-0002-5483-1972
Mario NegrelloDepartment of Neuroscience, Erasmus MC, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-8527-4259
Ben Torben-NielsenNeurolinx Research Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0003-4203-9942
Marylka Yoe UusisaariNeuronal Rhythms in Movement Unit, Okinawa Institute of Science and Technology Graduate University, Onna, Okinawa, 904-0495, Japan. uusisaari@oist.jp.ORCID http://orcid.org/0000-0001-6639-2789
Netherlands Institute for Neuroscience · NLHebrew University of Jerusalem · ILOkinawa Institute of Science and Technology Graduate University · JPErasmus MC · NLNeuroLinx Research Institute · US

Funding

European Research Council 294775European Research Council 758914European Research Council 768914H2020 Marie Skłodowska-Curie Actions 704922Israel Science Foundation (IL) 1496 2016NWO-ALW 854.10.004ZonMw 91210067
6 · The paper itself

Abstract

The inferior olive (IO) is an evolutionarily conserved brain stem structure and its output activity plays a major role in the cerebellar computation necessary for controlling the temporal accuracy of motor behavior. The precise timing and synchronization of IO network activity has been attributed to the dendro-dendritic gap junctions mediating electrical coupling within the IO nucleus. Thus, the dendritic morphology and spatial arrangement of IO neurons governs how synchronized activity emerges in this nucleus. To date, IO neuron structural properties have been characterized in few studies and with small numbers of neurons; these investigations have described IO neurons as belonging to two morphologically distinct types, "curly" and "straight". In this work we collect a large number of individual IO neuron morphologies visualized using different labeling techniques and present a thorough examination of their morphological properties and spatial arrangement within the olivary neuropil. Our results show that the extensive heterogeneity in IO neuron dendritic morphologies occupies a continuous range between the classically described "curly" and "straight" types, and that this continuum is well represented by a relatively simple measure of "straightness". Furthermore, we find that IO neuron dendritic trees are often directionally oriented. Combined with an examination of cell body density distributions and dendritic orientation of adjacent IO neurons, our results suggest that the IO network may be organized into groups of densely coupled neurons interspersed with areas of weaker coupling.

Indexed as

DendritesAnimalsFemaleImaging, Three-DimensionalMaleMiceNeuronsOlivary NucleusPrincipal Component AnalysisBrainstemDendritic morphometryNetwork structureNeuron reconstructionsOlivo-cerebellar systemSparse viral labeling

Identifiers

PMID30929054
PMCPMC6509097
OpenAlexW2927500404

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.