Evidence map›Paper›PMID 26129651›Full record

ArticleMucosal immunology2016

Interaction of IFN-γ with cholinergic agonists to modulate rat and human goblet cell function.

L García-Posadas, R R Hodges, D Li, M A Shatos, T Storr-Paulsen, Y Diebold, D A Dartt

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. CD8American journal of translational research · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Resolvin D2 uses multiple CaJournal of cellular physiology · 2022
    Article
  13. Review
  14. Review
  15. Impact of P2XInternational journal of molecular sciences · 2021
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. The cornea in keratoconjunctivitis sicca.Experimental eye research · 2020
    Review
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

7 authors at 4 institutions in 2 countries.

L García-PosadasOcular Surface Group, Institute for Applied Ophthalmobiology (IOBA), University of Valladolid, Valladolid, Spain.
R R HodgesSchepens Eye Research Institute/Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
D LiSchepens Eye Research Institute/Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
M A ShatosSchepens Eye Research Institute/Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
T Storr-PaulsenSchepens Eye Research Institute/Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
Y DieboldOcular Surface Group, Institute for Applied Ophthalmobiology (IOBA), University of Valladolid, Valladolid, Spain.
D A DarttSchepens Eye Research Institute/Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
Harvard University · USSmith-Kettlewell Eye Research Institute · USUniversidad de Valladolid · ESMassachusetts Eye and Ear Infirmary · US

Funding

Conjunctival Goblet Cell Mucin Secretion in Inflammation and Its ResolutionR01EY019470 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI DARTT, DARLENE A · 2009 to 2023
$7.4M
NEI NIH HHS EY019470NEI NIH HHS R01 EY019470
6 · The paper itself

Abstract

Goblet cells populate wet-surfaced mucosa including the conjunctiva of the eye, intestine, and nose, among others. These cells function as part of the innate immune system by secreting high molecular weight mucins that interact with environmental constituents including pathogens, allergens, and particulate pollutants. Herein, we determined whether interferon gamma (IFN-γ), a Th1 cytokine increased in dry eye, alters goblet cell function. Goblet cells from rat and human conjunctiva were cultured. Changes in intracellular [Ca(2+)] ([Ca(2+)](i)), high molecular weight glycoconjugate secretion, and proliferation were measured after stimulation with IFN-γ with or without the cholinergic agonist carbachol. IFN-γ itself increased [Ca(2+)](i) in rat and human goblet cells and prevented the increase in [Ca(2+)](i) caused by carbachol. Carbachol prevented IFN-γ-mediated increase in [Ca(2+)](i). This cross-talk between IFN-γ and muscarinic receptors may be partially due to use of the same Ca(2+)(i) reservoirs, but also from interaction of signaling pathways proximal to the increase in [Ca(2+)](i). IFN-γ blocked carbachol-induced high molecular weight glycoconjugate secretion and reduced goblet cell proliferation. We conclude that increased levels of IFN-γ in dry eye disease could explain the lack of goblet cells and mucin deficiency typically found in this pathology. IFN-γ could also function similarly in respiratory and gastrointestinal tracts.

Indexed as

AnimalsCalciumCalcium SignalingCarbacholCell Culture TechniquesCell ProliferationCholinergic AgonistsConjunctivaDrug InteractionsDry Eye SyndromesGene Expression RegulationGlyceraldehyde-3-Phosphate Dehydrogenase (NADP+)(Phosphorylating)GlycoconjugatesGoblet CellsHumansInterferon-gammaCalciumCarbacholCholinergic AgonistsGlyceraldehyde-3-Phosphate Dehydrogenase (NADP+)(Phosphorylating)GlycoconjugatesInterferon-gammaMUC5AC protein, humanMucin 5AC

Identifiers

PMID26129651
PMCPMC4698109
OpenAlexW2202085130

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.