Evidence map›Paper›PMID 26474499›Full record

ArticleGene expression patterns : GEP

Neuregulin1 and ErbB expression in the uninjured and regenerating olfactory mucosa.

M A Gilbert, B Lin, J Peterson, W Jang, J E Schwob

Open access · greenAbstract read
In one paragraph

Article in Gene expression patterns : GEP. 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
0.2field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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 1 institution in 1 country.

M A GilbertDepartment of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA 02111, USA; Genetics Program, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, MA 02111, USA.
B LinDepartment of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA 02111, USA; Cell, Molecular, and Developmental Biology, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, MA 02111, USA.
J PetersonDepartment of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA 02111, USA; Cell, Molecular, and Developmental Biology, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, MA 02111, USA.
W JangDepartment of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA 02111, USA.
J E SchwobDepartment of Developmental, Molecular, and Chemical Biology, Tufts University School of Medicine, Boston, MA 02111, USA. Electronic address: jim.schwob@tufts.edu.
Tufts University · US

Funding

REGULATION OF NEUROGENESIS IN OLFACTORY EPITHELIUMR01DC002167 · NIDCD · UPSTATE MEDICAL UNIVERSITY · PI SCHWOB, JAMES E. · 1994 to 2016
$5.2M
Regulation of Growth and Differentiation in 3-D Cultures of Olfactory EpitheliumR21DC010920 · NIDCD · TUFTS UNIVERSITY BOSTON · PI SCHWOB, JAMES E. · 2011 to 2012
$454k
Regulation of epitheliopoiesis in the olfactory epithelium by Neuregulin signalinF31DC012470 · NIDCD · TUFTS UNIVERSITY BOSTON · PI GILBERT, MELISSA ANN · 2012 to 2013
$76k
Olfactory Stem and Progenitor Cell PlasticityF31DC014637 · NIDCD · TUFTS UNIVERSITY BOSTON · PI LIN, BRIAN · 2015 to 2016
$72k
NIDCD NIH HHS 1F31DC012470NIDCD NIH HHS F31 DC012470NIDCD NIH HHS F31 DC014637NIDCD NIH HHS R01 DC002167NIDCD NIH HHS R01DC002167NIDCD NIH HHS R21 DC010920
6 · The paper itself

Abstract

Neuregulin1, a protein involved in signaling through the ErbB receptors, is required for the proper development of multiple organ systems. A complete understanding of the expression profile of Neuregulin1 is complicated by the presence of multiple isoform variants that result from extensive alternative splicing. Remarkably, these numerous protein products display a wide range of divergent functional roles, making the characterization of tissue-specific isoforms critical to understanding signaling. Recent evidence suggests an important role for Neuregulin1 signaling during olfactory epithelium development and regeneration. In order to understand the physiological consequences of this signaling, we sought to identify the isoform-specific and cell type-specific expression pattern of Neuregulin1 in the adult olfactory mucosa using a combination of RT-qPCR, FACS, and immunohistochemistry. To complement this information, we also analyzed the cell-type specific expression patterns of the ErbB receptors using immunohistochemistry. We found that multiple Neuregulin1 isoforms, containing predominantly the Type I and Type III N-termini, are expressed in the uninjured olfactory mucosa. Specifically, we found that Type III Neuregulin1 is highly expressed in mature olfactory sensory neurons and Type I Neuregulin1 is highly expressed in duct gland cells. Surprisingly, the divergent localization of these Neuregulin isoforms and their corresponding ErbB receptors does not support a role for active signaling during normal turnover and maintenance of the olfactory mucosa. Conversely, we found that injury to the olfactory epithelium specifically upregulates the Neuregulin1 Type I isoform bringing the expression pattern adjacent to cells expressing both ErbB2 and ErbB3 which is compatible with active signaling, supporting a functional role for Neuregulin1 specifically during regeneration.

Indexed as

AnimalsExonsGene Expression RegulationGenes, erbBImmunohistochemistryMiceMice, Inbred C57BLMice, TransgenicNeuregulin-1Olfactory MucosaOlfactory Receptor NeuronsOncogene Proteins v-erbBProtein IsoformsRegenerationSignal TransductionNeuregulin-1Nrg1 protein, mouseOncogene Proteins v-erbBProtein IsoformsErbBIsoform analysisNeuregulin1Olfactory epithelium

Identifiers

PMID26474499
PMCPMC4662624
OpenAlexW2194571950

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.