Evidence map›Paper›PMID 39557622›Full record

ArticleThe European journal of neuroscience2024

Regulator of G protein signalling 14 (RGS14) protein expression profile in the adult mouse brain.

Sara N Bramlett, Shana M Fitzmaurice, Nicholas H Harbin, Wuji Yan, Charan Bandlamudi, G Emme Van Doorn, Yoland Smith, John R Hepler

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Sara N BramlettDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0002-5284-2053
Shana M FitzmauriceDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.
Nicholas H HarbinDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.
Wuji YanDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.
Charan BandlamudiDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.
G Emme Van DoornDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.
Yoland SmithEmory National Primate Research Center, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-8700-878X
John R HeplerDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0002-1090-2919

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Structure and Function of the G-alpha-i1:RGS14:H-Ras signaling complexR01NS037112 · NINDS · EMORY UNIVERSITY · PI HEPLER, JOHN R · 1998 to 2023
$7.2M
RGS14 Regulation of Hormone-sensitive NPT2A-mediated Phosphate TransportR01GM140632 · NIGMS · EMORY UNIVERSITY · PI FRIEDMAN, PETER A, HEPLER, JOHN R · 2021 to 2024
$1.8M
AMYLOD BETA-PEPTIDE SPECIFIC scFv ANTIBODIESR21AG023534 · NIA · UNIVERSITY OF MEXICO, UNAM · PI GEVORKIAN, GOAR · 2004 to 2005
$194k
Emory University Integrated Cellular Imaging Core Facility RRID:SCR_023534NIGMS NIH HHS R01 GM140632NIH Office of the Director P51OD011132NINDS NIH HHS R01NS037112US Department of Health and Human Services. National Institutes of Health. NIGMS GM140632-A1
6 · The paper itself

Abstract

Regulator of G protein signalling 14 (RGS14) is a multifunctional signalling protein that serves as a natural suppressor of synaptic plasticity in the mouse brain. Our previous studies showed that RGS14 is highly expressed in postsynaptic dendrites and spines of pyramidal neurons in hippocampal area CA2 of the developing mouse brain. However, our more recent work with monkey brain shows that RGS14 is found in multiple neuron populations throughout hippocampal area CA1 and CA2, caudate nucleus, putamen, globus pallidus, substantia nigra and amygdala. In the mouse brain, we also have observed RGS14 protein in discrete limbic regions linked to reward behaviour and addiction, including the central amygdala and the nucleus accumbens, but a comprehensive mapping of RGS14 protein expression in the adult mouse brain is lacking. Here, we report that RGS14 is more broadly expressed in mouse brain than previously known. Intense RGS14 staining is observed in specific neuron populations of the hippocampal formation, amygdala, septum, bed nucleus of stria terminalis and ventral striatum/nucleus accumbens. RGS14 is also observed in axon fibre tracts including the dorsal fornix, fimbria, stria terminalis and the ventrohippocampal commissure. Moderate RGS14 staining is observed in various other adjacent regions not previously reported. These findings show that RGS14 is expressed in brain regions that govern aspects of core cognitive functions such as sensory perception, emotion, memory, motivation and execution of actions and suggest that RGS14 may serve to suppress plasticity and filter inputs in these brain regions to set the overall tone on experience-to-action processes.

Indexed as

BrainMice, Inbred C57BLRGS ProteinsAnimalsMaleMiceNeuronsRgs14 protein, mouseRGS Proteinsbasal gangliaextended amygdalahippocampal formationnucleus accumbensRGS14

Identifiers

PMID39557622
PMCPMC13255216

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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.