Evidence map›Paper›PMID 30357510›Full record

ReviewHistochemistry and cell biology2018

Diversity of enteroendocrine cells investigated at cellular and subcellular levels: the need for a new classification scheme.

Linda J Fothergill, John B Furness

Abstract readReview
In one paragraph

Review in Histochemistry and cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 82 citations in OpenAlex.

  1. Regional organization of nutrient absorption across the small intestine.Nature reviews. Gastroenterology & hepatology · 2026
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  11. Lewy body diseases and the gut.Molecular neurodegeneration · 2025
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  20. A New Role for Endocrine Cells in the Intestinal Crypt.Cellular and molecular gastroenterology and hepatology · 2023
    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

2 authors at 1 institution in 1 country.

Linda J FothergillDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.
John B FurnessDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia. j.furness@unimelb.edu.au.ORCID http://orcid.org/0000-0002-0219-3438
The University of Melbourne · AU

Funding

Mapping Stomach Autonomic Circuitry and Function for Neuromodulation of Gastric DisordersOT2OD023847 · OD · PURDUE UNIVERSITY · PI POWLEY, TERRY L. · 2016 to 2021
$17.6M
National Institutes of Health 1OT2OD023847NIH HHS OT2 OD023847
6 · The paper itself

Abstract

Enteroendocrine cells were historically classified by a letter code, each linked to a single hormone, deduced to be the only hormone produced by the cell. One type, the L cell, was recognised to store and secrete two products, peptide YY (PYY) and glucagon-related peptides. Many other exceptions to the one-cell one-hormone classifications have been reported over the last 40 years or so, and yet the one-hormone dogma has persisted. In the last 6 years, a plethora of data has appeared that makes the concept unviable. Here, we describe the evidence that multiple hormone transcripts and their products reside in single cells and evidence that the hormones are often, but not always, processed into separate storage vesicles. It has become clear that most enteroendocrine cells contain multiple hormones. For example, most secretin cells contain 5-hydroxytryptamine (5-HT), and in mouse many of these also contain cholecystokinin (CCK). Furthermore, CCK cells also commonly store ghrelin, glucose-dependent insulinotropic peptide (GIP), glucagon-like peptide-1 (GLP-1), neurotensin, and PYY. Several hormones, for example, secretin and 5-HT, are in separate storage vesicles at a subcellular level. Hormone patterns can differ considerably between species. Another complication is that relative levels of expression vary substantially. This means that data are significantly influenced by the sensitivities of detection techniques. For example, a hormone that can be detected in storage vesicles by super-resolution microscopy may not be above threshold for detection by conventional fluorescence microscopy. New nomenclature for cell clusters with common attributes will need to be devised and old classifications abandoned.

Indexed as

AnimalsCholecystokininEnteroendocrine CellsGastric Inhibitory PolypeptideGlucagon-Like Peptide 1HumansSerotoninCholecystokininGastric Inhibitory PolypeptideGlucagon-Like Peptide 1SerotoninEnteroendocrine cellsGut hormonesStorage vesiclesSuper-resolution microscopy

Identifiers

PMID30357510
PMCPMC6447040
OpenAlexW2898204561

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.