Evidence map›Paper›PMID 32940450›Full record

ArticleACS nano2020

Nanotopography Enhances Dynamic Remodeling of Tight Junction Proteins through Cytosolic Liquid Complexes.

Xiao Huang, Xiaoyu Shi, Mollie Eva Hansen, Initha Setiady, Cameron L Nemeth, Anna Celli, Bo Huang, Theodora Mauro, Michael Koval, Tejal A Desai

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2020. 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, 27 citations in OpenAlex.

  1. Review
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  9. Mechanosensory entities and functionality of endothelial cells.Frontiers in cell and developmental biology · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Above the Matrix: Functional Roles for Apically Localized Integrins.Frontiers in cell and developmental biology · 2021
    Review
  14. Review
  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

10 authors at 2 institutions in 1 country.

Xiao HuangDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California 94158, United States.
Xiaoyu ShiDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California 94158, United States.
Mollie Eva HansenUC Berkeley-UCSF Graduate Program in Bioengineering, University of California, San Francisco, San Francisco, California 94158, United States.
Initha SetiadyDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California 94158, United States.
Cameron L NemethUC Berkeley-UCSF Graduate Program in Bioengineering, University of California, San Francisco, San Francisco, California 94158, United States.
Anna CelliDepartment of Dermatology, University of California, San Francisco, San Francisco, California 94158, United States.
Bo HuangDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California 94158, United States.ORCID 0000-0003-1704-4141
Theodora MauroDepartment of Dermatology, University of California, San Francisco, San Francisco, California 94158, United States.
Michael KovalDivision of Pulmonary, Allergy, and Critical Care Medicine and Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia 30322, United States.
Tejal A DesaiDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California 94158, United States.
University of California, San Francisco · USEmory University · US

Funding

Pathogenesis and Therapy of Ichthyosis in Disorders of Lipid MetabolismR01AR061106 · NIAMS · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI MAURO, THEODORA M · 2012 to 2022
$3.3M
ATP2A2-Regulated Keretinocyted Ca2+ Signaling MechanismsR01AR051930 · NIAMS · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI MAURO, THEODORA M · 2006 to 2019
$3.2M
Mechanisms of nanostructure-enhanced transepithelial drug deliveryR01EB018842 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DESAI, TEJAL A. · 2014 to 2017
$1.4M
Structure mapping of molecular complexes by super-resolution microscopyR01GM124334 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUANG, BO · 2018 to 2021
$1.3M
Elucidating How Primary Cilia Regulate Hedgehog Signaling by Super-Resolution MicroscopyR00GM126136 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI SHI, XIAOYU · 2020 to 2022
$746k
Elucidating How Primary Cilia Regulate Hedgehog Signaling by Super-Resolution MicroscopyK99GM126136 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHI, XIAOYU · 2018 to 2019
$128k
NIAMS NIH HHS R01 AR051930NIAMS NIH HHS R01 AR061106NIBIB NIH HHS R01 EB018842NIGMS NIH HHS K99 GM126136NIGMS NIH HHS R00 GM126136NIGMS NIH HHS R01 GM124334
6 · The paper itself

Abstract

Nanotopographic materials provide special biophysical stimuli that can regulate epithelial tight junctions and their barrier function. Through the use of total internal reflection fluorescence microscopy of live cells, we demonstrated that contact of synthetic surfaces with defined nanotopography at the apical surface of epithelial monolayers increased paracellular permeability of macromolecules. To monitor changes in tight junction morphology in live cells, we fluorescently tagged the scaffold protein zonula occludens-1 (ZO-1) through CRISPR/Cas9-based gene editing to enable live cell tracking of ZO-1 expressed at physiologic levels. Contact between cells and nanostructured surfaces destabilized junction-associated ZO-1 and promoted its arrangement into highly dynamic liquid cytosolic complexes with a 1-5 μm diameter. Junction-associated ZO-1 rapidly remodeled, and we observed the direct transformation of cytosolic complexes into junction-like structures. Claudin-family tight junction transmembrane proteins and F-actin also were associated with these ZO-1 containing cytosolic complexes. These data suggest that these cytosolic structures are important intermediates formed in response to nanotopographic cues that facilitate rapid tight junction remodeling in order to regulate paracellular permeability.

Indexed as

Tight Junction ProteinsTight JunctionsActin CytoskeletonEpithelial CellsPermeabilityPhosphoproteinsZonula Occludens-1 ProteinPhosphoproteinsTight Junction ProteinsZonula Occludens-1 Proteincytosolic complexdynamic remodelingnanotopographyparacellular permeabilitytight junction

Identifiers

PMID32940450
PMCPMC7606830
OpenAlexW3085017387

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.