Evidence map›Paper›PMID 18669621›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2008

Serotonin modifies cytoskeleton and brush-border membrane architecture in human intestinal epithelial cells.

Ravinder K Gill, Le Shen, Jerrold R Turner, Seema Saksena, Waddah A Alrefai, Nitika Pant, Ali Esmaili, Alka Dwivedi, Krishnamurthy Ramaswamy, Pradeep K Dudeja

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

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  5. 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

10 authors at 2 institutions in 1 country.

Ravinder K GillDept. of Medicine, Univ. of Illinois at Chicago, Medical Research Service, Jesse Brown VA Medical Center, 820 S. Damen Ave., Chicago, IL 60612, USA. rgill@uic.edu
Le Shen
Jerrold R Turner
Seema Saksena
Waddah A Alrefai
Nitika Pant
Ali Esmaili
Alka Dwivedi
Krishnamurthy Ramaswamy
Pradeep K Dudeja
University of Chicago · USUniversity of Illinois Chicago · US

Funding

Intestinal Anion Transporters: Function and RegulationR01DK054016 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DUDEJA, PRADEEP K · 1998 to 2022
$7.0M
Transcriptional Regulation of NHE-3 Isoform in Human IntestineP01DK067887 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HECHT, GAIL A · 2006 to 2011
$4.9M
TRANSPORT MECHANISMS IN THE SMALL INTESTINER01DK033349 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DUDEJA, PRADEEP K · 1986 to 2012
$3.8M
DRA GENE AND THE HUMAN INTESTINAL ANION TRANSPORTF32DK009930 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ALREFAI, WADDAH A · 1999 to 2001
$96k
NIDDK NIH HHS DK-074459NIDDK NIH HHS DK-09930NIDDK NIH HHS DK-33349NIDDK NIH HHS DK-54016NIDDK NIH HHS P01 DK-067887
6 · The paper itself

Abstract

Serotonin or 5-hydroxytryptamine (5-HT) influences numerous functions in the gastrointestinal tract. We previously demonstrated that 5-HT treatment of Caco-2 cells inhibited Na(+)/H(+) exchangers (NHE) and Cl(-)/OH(-) exchange activities via distinct signaling mechanisms. Since regulation of several ion transporters such as NHE3 is influenced by intact cytoskeleton, we hypothesized that 5-HT modifies actin cytoskeleton and/or brush-border membrane architecture via involvement of signaling pathways. Ultrastructural analysis showed that 5-HT (0.1 muM, 1 h) treatment of Caco-2 cells caused the apical membrane to assume a convex dome shape that was associated with shortening of microvilli. To examine whether these cellular architecture changes are cytoskeleton driven, we analyzed actin cytoskeleton by fluorescence microscopy. 5-HT induced basal stress fibers with prominent cortical actin filaments via 5-HT3 and 5-HT4 receptor subtypes. This induction was partially attenuated by chelation of intracellular Ca(2+) and PKCalpha inhibition (Go6976). In vitro assays revealed that PKCalpha interacted with actin and this association was increased by 5-HT. Our data provide novel evidence that 5-HT-induced signaling via 5-HT3/4 receptor subtypes to cause Ca(2+) and PKCalpha-dependent regulation of actin cytoskeleton may play an important role in modulation of ion transporters that contribute to pathophysiology of diarrheal conditions associated with elevated levels of 5-HT.

Indexed as

ActinsCaco-2 CellsCarbazolesCytoskeletonEgtazic AcidEnzyme ActivationHumansIntestinal MucosaMicroscopy, ConfocalMicroscopy, Electron, TransmissionMicrovilliProtein Kinase CProtein Kinase C-alphaProtein Kinase C-deltaSerotoninSignal Transduction1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl esterActinsCarbazolesEgtazic AcidGo 6976Protein Kinase CProtein Kinase C-alphaProtein Kinase C-deltaSerotoninSodium-Hydrogen Exchangers

Identifiers

PMID18669621
PMCPMC2575920
OpenAlexW1972800124

What OpenQuestion holds

Textmetadata
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.