Evidence map›Paper›PMID 28264072›Full record

ArticlePloS one2017

The brain-specific RasGEF very-KIND is required for normal dendritic growth in cerebellar granule cells and proper motor coordination.

Kanehiro Hayashi, Asako Furuya, Yuriko Sakamaki, Takumi Akagi, Yo Shinoda, Tetsushi Sadakata, Tsutomu Hashikawa, Kazuki Shimizu, Haruka Minami, Yoshitake Sano and 2 more

Abstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Molecular assemblies and pharmacology of cerebellar GABAProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Ras GEF Mouse Models for the Analysis of Ras Biology and Signaling.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. 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.

Kanehiro HayashiLaboratory for Molecular Neurogenesis, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Asako FuruyaLaboratory for Molecular Neurogenesis, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Yuriko SakamakiResearch Resource Center, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Takumi AkagiResearch Resource Center, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Yo ShinodaLaboratory for Molecular Neurogenesis, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Tetsushi SadakataLaboratory for Molecular Neurogenesis, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Tsutomu HashikawaResearch Resource Center, RIKEN Brain Science Institute, Wako, Saitama, Japan.
Kazuki ShimizuDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Noda, Chiba, Japan.
Haruka MinamiDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Noda, Chiba, Japan.
Yoshitake SanoDepartment of Applied Biological Science, Faculty of Science and Technology, Tokyo University of Science, Noda, Chiba, Japan.
Manabu NakayamaChromosome Engineering Team, Department of Technology Development, Kazusa DNA Research Institute, Kisarazu, Chiba, Japan.
Teiichi FuruichiLaboratory for Molecular Neurogenesis, RIKEN Brain Science Institute, Wako, Saitama, Japan.ORCID http://orcid.org/0000-0002-9676-1888

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Very-KIND/Kndc1/KIAA1768 (v-KIND) is a brain-specific Ras guanine nucleotide exchange factor carrying two sets of the kinase non-catalytic C-lobe domain (KIND), and is predominantly expressed in cerebellar granule cells. Here, we report the impact of v-KIND deficiency on dendritic and synaptic growth in cerebellar granule cells in v-KIND knockout (KO) mice. Furthermore, we evaluate motor function in these animals. The gross anatomy of the cerebellum, including the cerebellar lobules, layered cerebellar cortex and densely-packed granule cell layer, in KO mice appeared normal, and was similar to wild-type (WT) mice. However, KO mice displayed an overgrowth of cerebellar granule cell dendrites, compared with WT mice, resulting in an increased number of dendrites, dendritic branches and terminals. Immunoreactivity for vGluT2 (a marker for excitatory presynapses of mossy fiber terminals) was increased in the cerebellar glomeruli of KO mice, compared with WT mice. The postsynaptic density around the terminals of mossy fibers was also increased in KO mice. Although there were no significant differences in locomotor ability between KO and WT animals in their home cages or in the open field, young adult KO mice had an increased grip strength and a tendency to exhibit better motor performance in balance-related tests compared with WT animals. Taken together, our results suggest that v-KIND is required for compact dendritic growth and proper excitatory synaptic connections in cerebellar granule cells, which are necessary for normal motor coordination and balance.

Indexed as

Psychomotor PerformanceAnimalsAxonsBiomarkersBrainCerebellumDendritesExcitatory Postsynaptic PotentialsGuanine Nucleotide Exchange FactorsImmunohistochemistryMiceMice, KnockoutNerve Tissue ProteinsOrgan SpecificitySynapsesBiomarkersGuanine Nucleotide Exchange FactorsNerve Tissue Proteinsvery-KIND protein, mouse

Identifiers

PMID28264072
PMCPMC5338823

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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.