Evidence map›Paper›PMID 31795328›Full record

ReviewInternational journal of molecular sciences2019

Reciprocal Association between the Apical Junctional Complex and AMPK: A Promising Therapeutic Target for Epithelial/Endothelial Barrier Function?

Kazuto Tsukita, Tomoki Yano, Atsushi Tamura, Sachiko Tsukita

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Research progress of gut microbiota and obesity caused by high-fat diet.Frontiers in cellular and infection microbiology · 2023
    Review
  8. Review
  9. Review
  10. Dehydrocostus Lactone Attenuates Methicillin-ResistantInternational journal of molecular sciences · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

4 authors at 3 institutions in 1 country.

Kazuto TsukitaLaboratory of Biological Science, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0811, Japan.ORCID 0000-0002-6878-2155
Tomoki YanoLaboratory of Biological Science, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0811, Japan.
Atsushi TamuraLaboratory of Biological Science, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0811, Japan.
Sachiko TsukitaLaboratory of Biological Science, Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0811, Japan.
Teikyo University · JPKyoto University · JPThe University of Osaka · JP

Funding

Japan Society for the Promotion of Science JP19H05468
6 · The paper itself

Abstract

Epithelial/endothelial cells adhere to each other via cell-cell junctions including tight junctions (TJs) and adherens junctions (AJs). TJs and AJs are spatiotemporally and functionally integrated, and are thus often collectively defined as apical junctional complexes (AJCs), regulating a number of spatiotemporal events including paracellular barrier, selective permeability, apicobasal cell polarity, mechano-sensing, intracellular signaling cascades, and epithelial morphogenesis. Over the past 15 years, it has been acknowledged that adenosine monophosphate (AMP)-activated protein kinase (AMPK), a well-known central regulator of energy metabolism, has a reciprocal association with AJCs. Here, we review the current knowledge of this association and show the following evidences: (1) as an upstream regulator, AJs activate the liver kinase B1 (LKB1)-AMPK axis particularly in response to applied junctional tension, and (2) TJ function and apicobasal cell polarization are downstream targets of AMPK and are promoted by AMPK activation. Although molecular mechanisms underlying these phenomena have not yet been completely elucidated, identifications of novel AMPK effectors in AJCs and AMPK-driven epithelial transcription factors have enhanced our knowledge. More intensive studies along this line would eventually lead to the development of AMPK-based therapies, enabling us to manipulate epithelial/endothelial barrier function.

Indexed as

Adherens JunctionsAMP-Activated Protein KinasesAnimalsCell PolarityEndothelial CellsEnergy MetabolismEpithelial CellsHumansPermeabilitySignal TransductionTight JunctionsAMP-Activated Protein Kinasesadherens junctionAMP-activated protein kinase (AMPK)apical junctional complexparacellular barriertight junction

Identifiers

PMID31795328
PMCPMC6928779
OpenAlexW2990964074

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.