Evidence map›Paper›PMID 28658323›Full record

ArticlePloS one2017

Using c-kit to genetically target cerebellar molecular layer interneurons in adult mice.

Samantha B Amat, Matthew J M Rowan, Michael A Gaffield, Audrey Bonnan, Chikako Kikuchi, Hiroki Taniguchi, Jason M Christie

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

7 authors at 1 institution in 1 country.

Samantha B AmatMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.
Matthew J M RowanMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.
Michael A GaffieldMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.
Audrey BonnanMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.
Chikako KikuchiMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.
Hiroki TaniguchiMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.
Jason M ChristieMax Planck Florida Institute for Neuroscience, Jupiter, FL, United States of America.ORCID http://orcid.org/0000-0003-0276-2554
Max Planck Florida Institute for Neuroscience · US

Funding

Action Potential Signaling in Axons of CNS InterneuronsR01NS083894 · NINDS · MAX PLANCK FLORIDA CORPORATION · PI CHRISTIE, JASON M · 2013 to 2017
$2.1M
Local control of the action potential in axonsF32NS083127 · NINDS · MAX PLANCK FLORIDA CORPORATION · PI ROWAN, MATTHEW J.M. · 2014 to 2016
$169k
NINDS NIH HHS F32 NS083127NINDS NIH HHS R01 NS083894
6 · The paper itself

Abstract

The cerebellar system helps modulate and fine-tune motor action. Purkinje cells (PCs) provide the sole output of the cerebellar cortex, therefore, any cerebellar involvement in motor activity must be driven by changes in PC firing rates. Several different cell types influence PC activity including excitatory input from parallel fibers and inhibition from molecular layer interneurons (MLIs). Similar to PCs, MLI activity is driven by parallel fibers, therefore, MLIs provide feed-forward inhibition onto PCs. To aid in the experimental assessment of how molecular layer inhibition contributes to cerebellar function and motor behavior, we characterized a new knock-in mouse line with Cre recombinase expression under control of endogenous c-kit transcriptional machinery. Using these engineered c-Kit mice, we were able to obtain high levels of conditional MLI transduction in adult mice using Cre-dependent viral vectors without any PC or granule cell labeling. We then used the mouse line to target MLIs for activity perturbation in vitro using opto- and chemogenetics.

Indexed as

Action PotentialsAnimalsCerebellar CortexCerebellumInterneuronsMiceMice, TransgenicProto-Oncogene Proteins c-kitProto-Oncogene Proteins c-kit

Identifiers

PMID28658323
PMCPMC5489153
OpenAlexW2731873846

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.