Evidence map›Paper›PMID 32074109›Full record

ArticlePloS one2020

Validating indicators of CNS disorders in a swine model of neurological disease.

Vicki J Swier, Katherine A White, David K Meyerholz, Aude Chefdeville, Rajesh Khanna, Jessica C Sieren, Dawn E Quelle, Jill M Weimer

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. NF1Clinical and translational science · 2024
    Article
  2. Article
  3. A Novel Porcine Model of CLN2 Batten Disease that Recapitulates Patient Phenotypes.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    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 4 institutions in 1 country.

Vicki J SwierPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, United States of America.
Katherine A WhitePediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, United States of America.
David K MeyerholzDepartment of Pathology, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.
Aude ChefdevilleDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona, United States of America.
Rajesh KhannaDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona, United States of America.
Jessica C SierenDepartment of Radiology and Biomedical Engineering, University of Iowa, Iowa City, Iowa, United States of America.
Dawn E QuelleDepartment of Pathology, University of Iowa Carver College of Medicine, Iowa City, Iowa, United States of America.
Jill M WeimerPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, United States of America.ORCID 0000-0003-2504-4942
University of Iowa · USSanford Research · USUniversity of Arizona · USUniversity of South Dakota · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
Respiratory virus infection in early cystic fibrosis lung diseaseP01HL091842 · NHLBI · UNIVERSITY OF IOWA · PI ZABNER, JOSEPH · 2008 to 2022
$34.2M
Yeast 2 HybridP20GM103620 · NIGMS · SANFORD RESEARCH/USD · PI ROUX, KYLE J · 2013 to 2023
$24.2M
The Impact of PD-1 Inhibition on Immune-Response to ChemoradiotherapyP20GM103548 · NIGMS · SANFORD RESEARCH/USD · PI MISKIMINS, W KEITH · 2012 to 2020
$20.8M
NHLBI NIH HHS P01 HL091842NIEHS NIH HHS P30 ES005605NIGMS NIH HHS P20 GM103548NIGMS NIH HHS P20 GM103620
6 · The paper itself

Abstract

Genetically modified swine disease models are becoming increasingly important for studying molecular, physiological and pathological characteristics of human disorders. Given the limited history of these model systems, there remains a great need for proven molecular reagents in swine tissue. Here, to provide a resource for neurological models of disease, we validated antibodies by immunohistochemistry for use in examining central nervous system (CNS) markers in a recently developed miniswine model of neurofibromatosis type 1 (NF1). NF1 is an autosomal dominant tumor predisposition disorder stemming from mutations in NF1, a gene that encodes the Ras-GTPase activating protein neurofibromin. Patients classically present with benign neurofibromas throughout their bodies and can also present with neurological associated symptoms such as chronic pain, cognitive impairment, and behavioral abnormalities. As validated antibodies for immunohistochemistry applications are particularly difficult to find for swine models of neurological disease, we present immunostaining validation of antibodies implicated in glial inflammation (CD68), oligodendrocyte development (NG2, O4 and Olig2), and neuron differentiation and neurotransmission (doublecortin, GAD67, and tyrosine hydroxylase) by examining cellular localization and brain region specificity. Additionally, we confirm the utility of anti-GFAP, anti-Iba1, and anti-MBP antibodies, previously validated in swine, by testing their immunoreactivity across multiple brain regions in mutant NF1 samples. These immunostaining protocols for CNS markers provide a useful resource to the scientific community, furthering the utility of genetically modified miniswine for translational and clinical applications.

Indexed as

AnimalsBiomarkersBrainCalcitonin Gene-Related PeptideCell LineageDisease Models, AnimalGlial Fibrillary Acidic ProteinMicrofilament ProteinsMicrogliaNeurofibromatosis 1Neurofibromin 1Oligodendrocyte Transcription Factor 2OligodendrogliaSwineBiomarkersCalcitonin Gene-Related PeptideGlial Fibrillary Acidic ProteinMicrofilament ProteinsNeurofibromin 1Oligodendrocyte Transcription Factor 2

Identifiers

PMID32074109
PMCPMC7029865
OpenAlexW3008881805

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.