Evidence map›Paper›PMID 21688022›Full record

ArticleHistochemistry and cell biology2011

Gastric tuft cells express DCLK1 and are expanded in hyperplasia.

Milena Saqui-Salces, Theresa M Keeley, Ann S Grosse, Xiaotan T Qiao, Mohamad El-Zaatari, Deborah L Gumucio, Linda C Samuelson, Juanita L Merchant

Open access · greenAbstract read
In one paragraph

Article in Histochemistry and cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

86 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
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  9. Article
  10. Intestinal Tuft Cells Are Enriched With Protocadherins.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2024
    Article
  11. Review
  12. G protein subunit GeLife · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Dynamic tuft cell expansion during gastric metaplasia and dysplasia.The journal of pathology. Clinical research · 2024
    Article
  19. Article
  20. Article

26 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Milena Saqui-SalcesDepartment of Internal Medicine, University of Michigan, 109 Zina Pitcher Pl. BSRBI, Rm.2051, Ann Arbor, MI 48109-2200, USA.
Theresa M Keeley
Ann S Grosse
Xiaotan T Qiao
Mohamad El-Zaatari
Deborah L Gumucio
Linda C Samuelson
Juanita L Merchant
University of Michigan–Ann Arbor · US

Funding

University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OMARY, BISHR · 1986 to 2021
$22.5M
Role of Hedgehog Signaling in Chronic Gastritis and MetaplasiaP01DK062041 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUMUCIO, DEBORAH L. · 2002 to 2017
$20.6M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Transcriptional Control of GastrinR37DK045729 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MERCHANT, JUANITA L. · 2007 to 2016
$3.4M
Mechanisms of Gastric Mucosal Transformation in Hip1r-Deficient MiceR01DK078927 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SAMUELSON, LINDA C. · 2008 to 2012
$1.6M
NIDDK NIH HHS P01 DK062041NIDDK NIH HHS P01-DK62041NIDDK NIH HHS P30 DK034933NIDDK NIH HHS P30-DK-34933NIDDK NIH HHS R01-DK078926NIDDK NIH HHS R01 DK078927NIDDK NIH HHS R37 DK045729NIGMS NIH HHS T32 GM007315
6 · The paper itself

Abstract

Epithelial tuft cells are named after their characteristic microtubule bundles located at the cell apex where these are exposed to the luminal environment. As such, tuft cells are found in multiple organs, including the gastrointestinal (GI) tract where the apical "tuft" is hypothesized to detect and transmit environmental signals. Thus, the goal of our study was to characterize gastric tuft cells during GI tract development, then subsequently in the normal and metaplastic adult stomach. GI tracts from mouse embryos, and newborn and postnatal mice were analyzed. Tuft cells were identified by immunohistochemistry using acetylated-α-tubulin (acTub) antibody to detect the microtubule bundle. Additional tuft cell markers, e.g., doublecortin-like kinase 1 (DCLK1), were used to co-localize with acTub. Tuft cells were quantified in human gastric tissue arrays and in mouse stomachs with or without inflammation. In the developing intestine, tuft cells in both the crypts and villi expressed all markers by E18.5. In the stomach, acTub co-localized with DCLK1 and other established tuft cell markers by E18.5 in the antrum, but not until postnatal day 7 in the corpus, with the highest density of tuft cells clustered at the forestomach ridge. Tuft cell numbers increased in hyperplastic human and mouse stomachs. In the adult GI tract, the tuft cell marker acTub co-expressed with DCKL1 and chemosensory markers, e.g.,TRPM5. In summary, tuft cells appear in the gastric antrum and intestine at E18.5, but their maximal numbers in the corpus are not achieved until after weaning. Tuft cell numbers increase with inflammation, hyperplasia, and metaplasia.

Indexed as

AnimalsChemoreceptor CellsDoublecortin-Like KinasesEpithelial CellsGastric MucosaGastritisGastrointestinal TractHumansHyperplasiaImmunohistochemistryMetaplasiaMiceProtein Serine-Threonine KinasesPyloric AntrumTRPM Cation ChannelsDclk1 protein, mouseDoublecortin-Like KinasesProtein Serine-Threonine KinasesTRPM5 protein, humanTRPM Cation Channels

Identifiers

PMID21688022
PMCPMC3570962
OpenAlexW2090279335

What OpenQuestion holds

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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.