Evidence map›Paper›PMID 38270517›Full record

ArticleeLife2024

A system of feed-forward cerebellar circuits that extend and diversify sensory signaling.

Harsh N Hariani, A Brynn Algstam, Christian T Candler, Isabelle F Witteveen, Jasmeen K Sidhu, Timothy S Balmer

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Balance performance in aged mice is dependent on unipolar brush cells.bioRxiv : the preprint server for biology · 2024
    Article
  4. Review
  5. Review
  6. Review
  7. A Continuum of Response Properties across the Population of Unipolar Brush Cells in the Dorsal Cochlear Nucleus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Harsh N HarianiInterdisciplinary Graduate Program in Neuroscience, Arizona State University, Tempe, United States.
A Brynn AlgstamSchool of Life Sciences, Arizona State University, Tempe, United States.
Christian T CandlerInterdisciplinary Graduate Program in Neuroscience, Arizona State University, Tempe, United States.
Isabelle F WitteveenSchool of Life Sciences, Arizona State University, Tempe, United States.
Jasmeen K SidhuSchool of Life Sciences, Arizona State University, Tempe, United States.
Timothy S BalmerSchool of Life Sciences, Arizona State University, Tempe, United States.ORCID https://orcid.org/0000-0002-8864-5465
Arizona State University · USBarrett Technology (United States) · US

Funding

Identification of inputs to unipolar brush cells and their roles in multisensory processingR00DC016905 · NIDCD · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI BALMER, TIMOTHY S · 2021 to 2023
$747k
Identification of inputs to unipolar brush cells and their roles in multisensory processingK99DC016905 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI BALMER, TIMOTHY S · 2019 to 2020
$251k
NIDCD NIH HHS DC016905NIDCD NIH HHS K99 DC016905NIDCD NIH HHS R00 DC016905
6 · The paper itself

Abstract

Sensory signals are processed by the cerebellum to coordinate movements. Numerous cerebellar functions are thought to require the maintenance of a sensory representation that extends beyond the input signal. Granule cells receive sensory input, but they do not prolong the signal and are thus unlikely to maintain a sensory representation for much longer than the inputs themselves. Unipolar brush cells (UBCs) are excitatory interneurons that project to granule cells and transform sensory input into prolonged increases or decreases in firing, depending on their ON or OFF UBC subtype. Further extension and diversification of the input signal could be produced by UBCs that project to one another, but whether this circuitry exists is unclear. Here we test whether UBCs innervate one another and explore how these small networks of UBCs could transform spiking patterns. We characterized two transgenic mouse lines electrophysiologically and immunohistochemically to confirm that they label ON and OFF UBC subtypes and crossed them together, revealing that ON and OFF UBCs innervate one another. A Brainbow reporter was used to label UBCs of the same ON or OFF subtype with different fluorescent proteins, which showed that UBCs innervate their own subtypes as well. Computational models predict that these feed-forward networks of UBCs extend the length of bursts or pauses and introduce delays-transformations that may be necessary for cerebellar functions from modulation of eye movements to adaptive learning across time scales.

Indexed as

CerebellumColoring AgentsAnimalsEye MovementsInterneuronsLearningMiceMice, TransgenicColoring AgentsBrainbowcerebellummossy fibermouseneurosciencesynapseunipolar brush cell

Identifiers

PMID38270517
PMCPMC10945699
OpenAlexW4385840224

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.