Evidence map›Paper›PMID 20961289›Full record

ArticleThe Biochemical journal2011

Contrasting effects of ERK on tight junction integrity in differentiated and under-differentiated Caco-2 cell monolayers.

Sudhir Aggarwal, Takuya Suzuki, William L Taylor, Aditi Bhargava, Radhakrishna K Rao

Open access · greenAbstract read
In one paragraph

Article in The Biochemical journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.7field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  9. Review
  10. Article
  11. Epithelial barriers in allergy and asthma.The Journal of allergy and clinical immunology · 2020
    Review
  12. Article
  13. Article
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  15. Article
  16. Zinc ameliorates intestinal barrier dysfunctions in shigellosis by reinstating claudin-2 and -4 on the membranes.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  17. Article
  18. Article
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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

5 authors at 2 institutions in 1 country.

Sudhir AggarwalDepartment of Physiology, University of Tennessee Health Sciences Center, Memphis, TN 38163, USA.
Takuya Suzuki
William L Taylor
Aditi Bhargava
Radhakrishna K Rao
University of Tennessee Health Science Center · USUniversity of California, San Francisco · US

Funding

INTESTINAL MUCOSAL PROTECTION BY EPIDERMAL GROWTH FACTORR01DK055532 · NIDDK · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI RAO, RADHAKRISHNA · 1998 to 2020
$4.7M
MECHANISM OF ENDOTOXIN ABSORPTION IN ALCOHOLISMR01AA012307 · NIAAA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI RAO, RADHAKRISHNA · 2000 to 2014
$3.9M
Regulation and Function of Urocortins and their ReceptorsR01DK080787 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BHARGAVA, ADITI · 2009 to 2013
$2.2M
NIAAA NIH HHS R01 AA012307NIAAA NIH HHS R01-AA12307NIDDK NIH HHS R01 DK055532NIDDK NIH HHS R01 DK080787NIDDK NIH HHS R01-DK080787NIDDK NIH HHS R01-DK55532
6 · The paper itself

Abstract

ERK (extracellular-signal-regulated kinase) activation leads to disruption of tight junctions in some epithelial monolayers, whereas it prevents disruption of tight junctions in other epithelia. The factors responsible for such contrasting influences of ERK on tight junction integrity are unknown. The present study investigated the effect of the state of cell differentiation on ERK-mediated regulation of tight junctions in Caco-2 cell monolayers. EGF (epidermal growth factor) potentiated H2O2-induced tight junction disruption in under-differentiated cell monolayers, which was attenuated by the MEK [MAPK (mitogen-activated protein kinase)/ERK kinase] inhibitor U0126. In contrast, EGF prevented H2O2-induced disruption of tight junctions in differentiated cell monolayers, which was also attenuated by U0126. Knockdown of ERK1/2 enhanced tight junction integrity and accelerated assembly of tight junctions in under-differentiated cell monolayers, whereas it had the opposite effect in differentiated cell monolayers. Regulated expression of wild-type and constitutively active MEK1 disrupted tight junctions, and the expression of dominant-negative MEK1 enhanced tight junction integrity in under-differentiated cells, whereas contrasting responses were recorded in differentiated cells. EGF prevented both H2O2-induced association of PP2A (protein phosphatase 2A), and loss of association of PKCζ (protein kinase Cζ), with occludin by an ERK-dependent mechanism in differentiated cell monolayers, but not in under-differentiated cell monolayers. Active ERK was distributed in the intracellular compartment in under-differentiated cell monolayers, whereas it was localized mainly in the perijunctional region in differentiated cell monolayers. Thus ERK may exhibit its contrasting influences on tight junction integrity in under-differentiated and differentiated epithelial cells by virtue of differences in its subcellular distribution and ability to regulate the association of PKCζ and PP2A with tight junction proteins.

Indexed as

Tight JunctionsCaco-2 CellsCell DifferentiationEpithelial CellsExtracellular Signal-Regulated MAP KinasesHumansMAP Kinase Kinase 1Protein BindingProtein Kinase CProtein Kinase C zetaProtein Phosphatase 2Tissue DistributionExtracellular Signal-Regulated MAP KinasesMAP Kinase Kinase 1Protein Kinase CProtein Kinase C zetaProtein Phosphatase 2

Identifiers

PMID20961289
PMCPMC4438673
OpenAlexW2040439274

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.