Evidence map›Paper›PMID 30037345›Full record

ArticleActa neuropathologica communications2018

Characterisation of tau in the human and rodent enteric nervous system under physiological conditions and in tauopathy.

Arthur Lionnet, Matthew A Wade, Anne-Gaëlle Corbillé, Alice Prigent, Sébastien Paillusson, Maddalena Tasselli, Jacques Gonzales, Emilie Durieu, Malvyne Rolli-Derkinderen, Emmanuel Coron and 6 more

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

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  16. Gastrointestinal mucosal biopsies in Parkinson's disease: beyond alpha-synuclein detection.Journal of neural transmission (Vienna, Austria : 1996) · 2022
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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

16 authors at 3 institutions in 2 countries.

Arthur LionnetInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Matthew A WadeKing's College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, Rm 1.23, 5 Cutcombe Road, Camberwell, London, SE5 9RX, UK.
Anne-Gaëlle CorbilléInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Alice PrigentInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Sébastien PaillussonKing's College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, Rm 1.23, 5 Cutcombe Road, Camberwell, London, SE5 9RX, UK.
Maddalena TasselliKing's College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, Rm 1.23, 5 Cutcombe Road, Camberwell, London, SE5 9RX, UK.
Jacques GonzalesInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Emilie DurieuInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Malvyne Rolli-DerkinderenInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Emmanuel CoronInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Emilie DuchalaisInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Michel NeunlistInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France.
Michael S PerkintonNeuroscience, IMED Biotech Unit, AstraZeneca, Cambridge, CB21 6GH, UK.
Diane P HangerKing's College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, Rm 1.23, 5 Cutcombe Road, Camberwell, London, SE5 9RX, UK.
Wendy NobleKing's College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, Maurice Wohl Clinical Neuroscience Institute, Rm 1.23, 5 Cutcombe Road, Camberwell, London, SE5 9RX, UK. Wendy.Noble@kcl.ac.uk.ORCID 0000-0002-7898-4295
Pascal DerkinderenInserm, U1235, 1 rue Gaston Veil, F-44035, Nantes, France. pascal.derkinderen@chu-nantes.fr.
Inserm · FRKing's College London · GBAstraZeneca (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L502601/1
6 · The paper itself

Abstract

Tau is normally a highly soluble phosphoprotein found predominantly in neurons. Six different isoforms of tau are expressed in the adult human CNS. Under pathological conditions, phosphorylated tau aggregates are a defining feature of neurodegenerative disorders called tauopathies. Recent findings have suggested a potential role of the gut-brain axis in CNS homeostasis, and therefore we set out to examine the isoform profile and phosphorylation state of tau in the enteric nervous system (ENS) under physiological conditions and in tauopathies. Surgical specimens of human colon from controls, Parkinson's disease (PD) and progressive supranuclear palsy (PSP) patients were analyzed by Western Blot and immunohistochemistry using a panel of anti-tau antibodies. We found that adult human ENS primarily expresses two tau isoforms, localized in the cell bodies and neuronal processes. We did not observe any difference in the enteric tau isoform profile and phosphorylation state between PSP, PD and control subjects. The htau mouse model of tauopathy also expressed two main isoforms of human tau in the ENS, and there were no apparent differences in ENS tau localization or phosphorylation between wild-type and htau mice. Tau in both human and mouse ENS was found to be phosphorylated but poorly susceptible to dephosphorylation with lambda phosphatase. To investigate ENS tau phosphorylation further, primary cultures from rat enteric neurons, which express four isoforms of tau, were pharmacologically manipulated to show that ENS tau phosphorylation state can be regulated, at least in vitro. Our study is the first to characterize tau in the rodent and human ENS. As a whole, our findings provide a basis to unravel the functions of tau in the ENS and to further investigate the possibility of pathological changes in enteric neuropathies and tauopathies.

Indexed as

AgedAnimalsAnti-Infective AgentsBenzophenanthridinesBrainCells, CulturedColonEmbryo, MammalianEnteric Nervous SystemFemaleHumansIsoquinolinesMaleMiceMice, TransgenicMiddle AgedAnti-Infective AgentsBenzophenanthridinesIsoquinolinesMapt protein, mouseProtein Isoformssanguinarinetau ProteinsTubulinUbiquitin ThiolesteraseUCHL1 protein, humanBiopsyEnteric nervous systemGutHtau mouseParkinson’s diseaseProgressive supranuclear palsyTauTau isoformTau phosphorylation

Identifiers

PMID30037345
PMCPMC6055332
OpenAlexW2883093512

What OpenQuestion holds

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LicenceCC BY
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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.