Evidence map›Paper›PMID 25870547›Full record

ArticleFrontiers in behavioral neuroscience2015

Conditional targeting of medium spiny neurons in the striatal matrix.

Björn Reinius, Martina Blunder, Frances M Brett, Anders Eriksson, Kalicharan Patra, Jörgen Jonsson, Elena Jazin, Klas Kullander

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  5. Review
  6. Review
  7. Frontiers in aging neuroscience · 2021
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  15. GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2016
    Article
  16. 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

8 authors at 1 institution in 1 country.

Björn ReiniusUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden ; Department of Organismal Biology, EBC, Uppsala University Uppsala, Sweden.
Martina BlunderUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden.
Frances M BrettUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden.
Anders ErikssonUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden.
Kalicharan PatraUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden.
Jörgen JonssonUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden.
Elena JazinDepartment of Organismal Biology, EBC, Uppsala University Uppsala, Sweden.
Klas KullanderUnit of Developmental Genetics, Department of Neuroscience, BMC, Uppsala University Uppsala, Sweden.
Uppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The striatum serves as the main input to the basal ganglia, and is key for the regulation of motor behaviors, compulsion, addiction, and various cognitive and emotional states. Its deterioration is associated with degenerative disorders such as Huntington's disease. Despite its apparent anatomical uniformity, it consists of intermingled cell populations, which have precluded straightforward anatomical sub-classifications adhering to functional dissections. Approximately 95% of the striatal neurons are inhibitory projection neurons termed medium spiny neurons (MSNs). They are commonly classified according to their expression of either dopamine receptor D1 or D2, which also determines their axonal projection patterns constituting the direct and indirect pathway in the basal ganglia. Immunohistochemical patterns have further indicated compartmentalization of the striatum to the striosomes and the surrounding matrix, which integrate MSNs of both the D1 and D2 type. Here, we present a transgenic mouse line, Gpr101-Cre, with Cre recombinase activity localized to matrix D1 and D2 MSNs. Using two Gpr101-Cre founder lines with different degrees of expression in the striatum, we conditionally deleted the vesicular inhibitory amino acid transporter (VIAAT), responsible for storage of GABA and glycine in synaptic vesicles. Partial ablation of VIAAT (in ~36% of MSNs) resulted in elevated locomotor activity compared to control mice, when provoked with the monoamine reuptake inhibitor cocaine. Near complete targeting of matrix MSNs led to profoundly changed motor behaviors, which increased in severity as the mice aged. Moreover, these mice had exaggerated muscle rigidity, retarded growth, increased rate of spontaneous deaths, and defective memory. Therefore, our data provide a link between dysfunctional GABA signaling of matrix MSNs to specific behavioral alterations, which are similar to the symptoms of Huntington's disease.

Indexed as

behaviorGABAhuntington's diseasematrixmedium spiny neuronpatchesSLC32A1striosome

Identifiers

PMID25870547
PMCPMC4375991
OpenAlexW1972728521

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.