Evidence map›Paper›PMID 25556545›Full record

ArticleThe Journal of comparative neurology2015

Evidence for limited D1 and D2 receptor coexpression and colocalization within the dorsal striatum of the neonatal mouse.

Dominik K Biezonski, Pierre Trifilieff, Jozsef Meszaros, Jonathan A Javitch, Christoph Kellendonk

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

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  16. Levodopa treatment and dendritic spine pathology.Movement disorders : official journal of the Movement Disorder Society · 2018
    Review
  17. Review
  18. Article
  19. Striatal Neurons Expressing DScientific reports · 2017
    Article
  20. 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

5 authors at 3 institutions in 2 countries.

Dominik K BiezonskiDepartment of Psychiatry, Division of Molecular Therapeutics, Columbia University, New York State Psychiatric Institute, New York, New York, 10032, USA.
Pierre Trifilieff
Jozsef Meszaros
Jonathan A Javitch
Christoph Kellendonk
Columbia University · USNew York State Psychiatric InstituteNew York Psychoanalytic Society and Institute · US

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Structure of the Dopamine D2-Like Receptor Binding SitesR01MH054137 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI JAVITCH, JONATHAN A · 1995 to 2025
$12.0M
Medium Spiny Neuron Excitability and MotivationR01MH093672 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI KELLENDONK, CHRISTOPH · 2011 to 2020
$5.0M
ADVANCED GRADUATE TRAINING PROGRAM IN NEUROBIOLOGY & BEHAVIORT32NS064928 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HENGST, ULRICH · 2010 to 2024
$3.0M
Molecular Determinants for the Action of PsychostimulantsK05DA022413 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JAVITCH, JONATHAN A · 2007 to 2016
$1.3M
NCI NIH HHS P30 CA013696NIDA NIH HHS DA022413NIDA NIH HHS K05 DA022413NIMH NIH HHS MH093672NIMH NIH HHS MH54137NIMH NIH HHS R01 MH054137NIMH NIH HHS R01 MH093672NINDS NIH HHS 5T32NS064928-04NINDS NIH HHS T32 NS064928PHS HHS T32 016434-33
6 · The paper itself

Abstract

The striatum is the major input nucleus of the basal ganglia involved in reward processing, goal-directed behaviors, habit learning, and motor control. The striatum projects to the basal ganglia output nuclei via the "direct" and "indirect" pathways, which can be distinguished by their projection fields and their opposing effects on behavior. In adult animals, the functional opposition is modulated by the differential actions of D1 and D2 dopamine receptors (D1R, D2R), the expression of which is largely separated between these pathways. To determine whether a similar degree of separation exists earlier in development, we used dual-label immunohistochemistry to map dorsal-striatal D1R and D2R expression at the promoter level in postnatal day 0 (PD0) Drd1a-tdTomato/Drd2-GFP BAC transgenic mice, and at the receptor level by costaining for native D1R and D2R in wildtype (WT) PD0 animals. To assess for potential molecular interactions between D1R and D2R we also employed a recently developed proximity-ligation assay (PLA). Limited coexpression and colocalization of the D1R and D2R proteins was found in clusters of neurons endemic to the "patch" compartment as identified by costaining with tyrosine hydroxylase, but not outside these clusters. Moreover, in contrast to our recent findings where we failed to detect a D1R-D2R PLA signal in the adult striatum, in PD0 striatum we did identify a clear PLA signal for this pair of receptors. This colocalization at close proximity points to a possible role for D1R/D2R-mediated crosstalk in early striatal ontogeny.

Indexed as

AnimalsAnimals, NewbornCorpus StriatumFluorescent Antibody TechniqueGreen Fluorescent ProteinsMice, Inbred C57BLMice, KnockoutMice, TransgenicMicroscopy, ConfocalNeuronsReceptors, Dopamine D1Receptors, Dopamine D2Tyrosine 3-MonooxygenaseDrd1 protein, mouseDRD2 protein, mouseGreen Fluorescent ProteinsReceptors, Dopamine D1Receptors, Dopamine D2Tyrosine 3-MonooxygenaseAB_10013483AB_10710873AB_1840787AB_2079751AB_300798dopamine receptorsIMSR_JAX:016204IMSR_MMRRC:000230matrixneonatenif-0000-30467nlx_153890patchproximity-ligation assayrid_000081RRID: AB_11213750striatum

Identifiers

PMID25556545
PMCPMC4390438
OpenAlexW1887895882

What OpenQuestion holds

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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.