Evidence map›Paper›PMID 27109921›Full record

ArticleNeuroscience2016

Neuronatin is a stress-responsive protein of rod photoreceptors.

Vishal Shinde, Priyamvada M Pitale, Wayne Howse, Oleg Gorbatyuk, Marina Gorbatyuk

Abstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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  7. Characteristic Localization of Neuronatin in Rat Testis, Hair Follicle, Tongue, and Pancreas.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2019
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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 1 institution in 1 country.

Vishal ShindeUniversity of Alabama at Birmingham, Department of Optometry, United States; University of Alabama at Birmingham, Department of Vision Science, School of Optometry, United States.
Priyamvada M PitaleUniversity of Alabama at Birmingham, Department of Optometry, United States; University of Alabama at Birmingham, Department of Vision Science, School of Optometry, United States.
Wayne HowseUniversity of Alabama at Birmingham, Department of Optometry, United States; University of Alabama at Birmingham, Department of Vision Science, School of Optometry, United States.
Oleg GorbatyukUniversity of Alabama at Birmingham, Department of Optometry, United States; University of Alabama at Birmingham, Department of Vision Science, School of Optometry, United States.
Marina GorbatyukUniversity of Alabama at Birmingham, Department of Optometry, United States; University of Alabama at Birmingham, Department of Vision Science, School of Optometry, United States. Electronic address: mgortk@uab.edu.
University of Alabama at Birmingham · US

Funding

Visual Phenotyping CoreP30EY003039 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LAWRENCE C SINCICH · 1985 to 2026
$16.9M
Unfolded Protein Response as a Therapeutic Target for ADRP Animal ModelsR01EY020905 · NEI · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI GORBATYUK, MARINA · 2010 to 2014
$1.3M
NEI NIH HHS P30 EY003039NEI NIH HHS R01 EY020905
6 · The paper itself

Abstract

Neuronatin (NNAT) is a small transmembrane proteolipid that is highly expressed in the embryonic developing brain and several other peripheral tissues. This study is the first to provide evidence that NNAT is detected in the adult retina of various adult rod-dominant mammals, including wild-type (WT) rodents, transgenic rodents expressing mutant S334ter, P23H, or T17M rhodopsin, non-human primates, humans, and cone-dominant tree shrews. Immunohistochemical and quantitative real time polymerase chain reaction (qRT-PCR) analyses were applied to detect NNAT. Confocal microscopy analysis revealed that NNAT immunofluorescence is restricted to the outer segments (OSs) of photoreceptors without evidence of staining in other retinal cell types across all mammalian species. Moreover, in tree shrew retinas, we found NNAT to be co-localized with rhodopsin, indicating its predominant expression in rods. The rod-derived expression of NNAT was further confirmed by qRT-PCR in isolated rod photoreceptor cells. We also used these cells to mimic cellular stress in transgenic retinas by treating them with the endoplasmic reticulum stress inducer, tunicamycin. Thus, our data revealed accumulation of NNAT around the nucleus as compared to dispersed localization of NNAT within control cells. This distribution coincided with the partial intracellular mislocalization of NNAT to the outer nuclear layer observed in transgenic retinas. In addition, stressed retinas demonstrated an increase of NNAT mRNA and protein levels. Therefore, our study demonstrated that NNAT is a novel stress-responsive protein with a potential structural and/or functional role in adult mammalian retinas.

Indexed as

AnimalsCells, CulturedDisease Models, AnimalEndoplasmic Reticulum StressFemaleGene Expression RegulationHumansMembrane ProteinsMice, Inbred C57BLMice, TransgenicMiddle AgedNerve Tissue ProteinsRats, Sprague-DawleyRats, TransgenicRetinal DegenerationRetinal Rod Photoreceptor CellsMembrane ProteinsNerve Tissue ProteinsNNAT protein, humanRNA, MessengerTunicamycinautosomal dominant retinitis pigmentosaER stressneuronatinretinal degenerationrod photoreceptors

Identifiers

PMID27109921
PMCPMC4879961
OpenAlexW2340885102

What OpenQuestion holds

Textmetadata
LicenceTDM
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.